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1,000 | cggh/scikit-allel | allel/chunked/core.py | store | def store(data, arr, start=0, stop=None, offset=0, blen=None):
"""Copy `data` block-wise into `arr`."""
# setup
blen = _util.get_blen_array(data, blen)
if stop is None:
stop = len(data)
else:
stop = min(stop, len(data))
length = stop - start
if length < 0:
raise ValueError('invalid stop/start')
# copy block-wise
for bi in range(start, stop, blen):
bj = min(bi+blen, stop)
bl = bj - bi
arr[offset:offset+bl] = data[bi:bj]
offset += bl | python | def store(data, arr, start=0, stop=None, offset=0, blen=None):
# setup
blen = _util.get_blen_array(data, blen)
if stop is None:
stop = len(data)
else:
stop = min(stop, len(data))
length = stop - start
if length < 0:
raise ValueError('invalid stop/start')
# copy block-wise
for bi in range(start, stop, blen):
bj = min(bi+blen, stop)
bl = bj - bi
arr[offset:offset+bl] = data[bi:bj]
offset += bl | [
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1,001 | cggh/scikit-allel | allel/chunked/core.py | copy | def copy(data, start=0, stop=None, blen=None, storage=None, create='array',
**kwargs):
"""Copy `data` block-wise into a new array."""
# setup
storage = _util.get_storage(storage)
blen = _util.get_blen_array(data, blen)
if stop is None:
stop = len(data)
else:
stop = min(stop, len(data))
length = stop - start
if length < 0:
raise ValueError('invalid stop/start')
# copy block-wise
out = None
for i in range(start, stop, blen):
j = min(i+blen, stop)
block = data[i:j]
if out is None:
out = getattr(storage, create)(block, expectedlen=length, **kwargs)
else:
out.append(block)
return out | python | def copy(data, start=0, stop=None, blen=None, storage=None, create='array',
**kwargs):
# setup
storage = _util.get_storage(storage)
blen = _util.get_blen_array(data, blen)
if stop is None:
stop = len(data)
else:
stop = min(stop, len(data))
length = stop - start
if length < 0:
raise ValueError('invalid stop/start')
# copy block-wise
out = None
for i in range(start, stop, blen):
j = min(i+blen, stop)
block = data[i:j]
if out is None:
out = getattr(storage, create)(block, expectedlen=length, **kwargs)
else:
out.append(block)
return out | [
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1,002 | cggh/scikit-allel | allel/chunked/core.py | copy_table | def copy_table(tbl, start=0, stop=None, blen=None, storage=None,
create='table', **kwargs):
"""Copy `tbl` block-wise into a new table."""
# setup
names, columns = _util.check_table_like(tbl)
storage = _util.get_storage(storage)
blen = _util.get_blen_table(tbl, blen)
if stop is None:
stop = len(columns[0])
else:
stop = min(stop, len(columns[0]))
length = stop - start
if length < 0:
raise ValueError('invalid stop/start')
# copy block-wise
out = None
for i in range(start, stop, blen):
j = min(i+blen, stop)
res = [c[i:j] for c in columns]
if out is None:
out = getattr(storage, create)(res, names=names,
expectedlen=length, **kwargs)
else:
out.append(res)
return out | python | def copy_table(tbl, start=0, stop=None, blen=None, storage=None,
create='table', **kwargs):
# setup
names, columns = _util.check_table_like(tbl)
storage = _util.get_storage(storage)
blen = _util.get_blen_table(tbl, blen)
if stop is None:
stop = len(columns[0])
else:
stop = min(stop, len(columns[0]))
length = stop - start
if length < 0:
raise ValueError('invalid stop/start')
# copy block-wise
out = None
for i in range(start, stop, blen):
j = min(i+blen, stop)
res = [c[i:j] for c in columns]
if out is None:
out = getattr(storage, create)(res, names=names,
expectedlen=length, **kwargs)
else:
out.append(res)
return out | [
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1,003 | cggh/scikit-allel | allel/chunked/core.py | map_blocks | def map_blocks(data, f, blen=None, storage=None, create='array', **kwargs):
"""Apply function `f` block-wise over `data`."""
# setup
storage = _util.get_storage(storage)
if isinstance(data, tuple):
blen = max(_util.get_blen_array(d, blen) for d in data)
else:
blen = _util.get_blen_array(data, blen)
if isinstance(data, tuple):
_util.check_equal_length(*data)
length = len(data[0])
else:
length = len(data)
# block-wise iteration
out = None
for i in range(0, length, blen):
j = min(i+blen, length)
# obtain blocks
if isinstance(data, tuple):
blocks = [d[i:j] for d in data]
else:
blocks = [data[i:j]]
# map
res = f(*blocks)
# store
if out is None:
out = getattr(storage, create)(res, expectedlen=length, **kwargs)
else:
out.append(res)
return out | python | def map_blocks(data, f, blen=None, storage=None, create='array', **kwargs):
# setup
storage = _util.get_storage(storage)
if isinstance(data, tuple):
blen = max(_util.get_blen_array(d, blen) for d in data)
else:
blen = _util.get_blen_array(data, blen)
if isinstance(data, tuple):
_util.check_equal_length(*data)
length = len(data[0])
else:
length = len(data)
# block-wise iteration
out = None
for i in range(0, length, blen):
j = min(i+blen, length)
# obtain blocks
if isinstance(data, tuple):
blocks = [d[i:j] for d in data]
else:
blocks = [data[i:j]]
# map
res = f(*blocks)
# store
if out is None:
out = getattr(storage, create)(res, expectedlen=length, **kwargs)
else:
out.append(res)
return out | [
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1,004 | cggh/scikit-allel | allel/chunked/core.py | reduce_axis | def reduce_axis(data, reducer, block_reducer, mapper=None, axis=None,
blen=None, storage=None, create='array', **kwargs):
"""Apply an operation to `data` that reduces over one or more axes."""
# setup
storage = _util.get_storage(storage)
blen = _util.get_blen_array(data, blen)
length = len(data)
# normalise axis arg
if isinstance(axis, int):
axis = (axis,)
# deal with 'out' kwarg if supplied, can arise if a chunked array is
# passed as an argument to numpy.sum(), see also
# https://github.com/cggh/scikit-allel/issues/66
kwarg_out = kwargs.pop('out', None)
if kwarg_out is not None:
raise ValueError('keyword argument "out" is not supported')
if axis is None or 0 in axis:
# two-step reduction
out = None
for i in range(0, length, blen):
j = min(i+blen, length)
block = data[i:j]
if mapper:
block = mapper(block)
res = reducer(block, axis=axis)
if out is None:
out = res
else:
out = block_reducer(out, res)
if np.isscalar(out):
return out
elif len(out.shape) == 0:
return out[()]
else:
return getattr(storage, create)(out, **kwargs)
else:
# first dimension is preserved, no need to reduce blocks
out = None
for i in range(0, length, blen):
j = min(i+blen, length)
block = data[i:j]
if mapper:
block = mapper(block)
r = reducer(block, axis=axis)
if out is None:
out = getattr(storage, create)(r, expectedlen=length, **kwargs)
else:
out.append(r)
return out | python | def reduce_axis(data, reducer, block_reducer, mapper=None, axis=None,
blen=None, storage=None, create='array', **kwargs):
# setup
storage = _util.get_storage(storage)
blen = _util.get_blen_array(data, blen)
length = len(data)
# normalise axis arg
if isinstance(axis, int):
axis = (axis,)
# deal with 'out' kwarg if supplied, can arise if a chunked array is
# passed as an argument to numpy.sum(), see also
# https://github.com/cggh/scikit-allel/issues/66
kwarg_out = kwargs.pop('out', None)
if kwarg_out is not None:
raise ValueError('keyword argument "out" is not supported')
if axis is None or 0 in axis:
# two-step reduction
out = None
for i in range(0, length, blen):
j = min(i+blen, length)
block = data[i:j]
if mapper:
block = mapper(block)
res = reducer(block, axis=axis)
if out is None:
out = res
else:
out = block_reducer(out, res)
if np.isscalar(out):
return out
elif len(out.shape) == 0:
return out[()]
else:
return getattr(storage, create)(out, **kwargs)
else:
# first dimension is preserved, no need to reduce blocks
out = None
for i in range(0, length, blen):
j = min(i+blen, length)
block = data[i:j]
if mapper:
block = mapper(block)
r = reducer(block, axis=axis)
if out is None:
out = getattr(storage, create)(r, expectedlen=length, **kwargs)
else:
out.append(r)
return out | [
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1,005 | cggh/scikit-allel | allel/chunked/core.py | amax | def amax(data, axis=None, mapper=None, blen=None, storage=None,
create='array', **kwargs):
"""Compute the maximum value."""
return reduce_axis(data, axis=axis, reducer=np.amax,
block_reducer=np.maximum, mapper=mapper,
blen=blen, storage=storage, create=create, **kwargs) | python | def amax(data, axis=None, mapper=None, blen=None, storage=None,
create='array', **kwargs):
return reduce_axis(data, axis=axis, reducer=np.amax,
block_reducer=np.maximum, mapper=mapper,
blen=blen, storage=storage, create=create, **kwargs) | [
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1,006 | cggh/scikit-allel | allel/chunked/core.py | amin | def amin(data, axis=None, mapper=None, blen=None, storage=None,
create='array', **kwargs):
"""Compute the minimum value."""
return reduce_axis(data, axis=axis, reducer=np.amin,
block_reducer=np.minimum, mapper=mapper,
blen=blen, storage=storage, create=create, **kwargs) | python | def amin(data, axis=None, mapper=None, blen=None, storage=None,
create='array', **kwargs):
return reduce_axis(data, axis=axis, reducer=np.amin,
block_reducer=np.minimum, mapper=mapper,
blen=blen, storage=storage, create=create, **kwargs) | [
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1,007 | cggh/scikit-allel | allel/chunked/core.py | asum | def asum(data, axis=None, mapper=None, blen=None, storage=None,
create='array', **kwargs):
"""Compute the sum."""
return reduce_axis(data, axis=axis, reducer=np.sum,
block_reducer=np.add, mapper=mapper,
blen=blen, storage=storage, create=create, **kwargs) | python | def asum(data, axis=None, mapper=None, blen=None, storage=None,
create='array', **kwargs):
return reduce_axis(data, axis=axis, reducer=np.sum,
block_reducer=np.add, mapper=mapper,
blen=blen, storage=storage, create=create, **kwargs) | [
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1,008 | cggh/scikit-allel | allel/chunked/core.py | count_nonzero | def count_nonzero(data, mapper=None, blen=None, storage=None,
create='array', **kwargs):
"""Count the number of non-zero elements."""
return reduce_axis(data, reducer=np.count_nonzero,
block_reducer=np.add, mapper=mapper,
blen=blen, storage=storage, create=create, **kwargs) | python | def count_nonzero(data, mapper=None, blen=None, storage=None,
create='array', **kwargs):
return reduce_axis(data, reducer=np.count_nonzero,
block_reducer=np.add, mapper=mapper,
blen=blen, storage=storage, create=create, **kwargs) | [
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1,009 | cggh/scikit-allel | allel/chunked/core.py | subset | def subset(data, sel0=None, sel1=None, blen=None, storage=None, create='array',
**kwargs):
"""Return selected rows and columns of an array."""
# TODO refactor sel0 and sel1 normalization with ndarray.subset
# setup
storage = _util.get_storage(storage)
blen = _util.get_blen_array(data, blen)
length = len(data)
if sel0 is not None:
sel0 = np.asanyarray(sel0)
if sel1 is not None:
sel1 = np.asanyarray(sel1)
# ensure boolean array for dim 0
if sel0 is not None and sel0.dtype.kind != 'b':
# assume indices, convert to boolean condition
tmp = np.zeros(length, dtype=bool)
tmp[sel0] = True
sel0 = tmp
# ensure indices for dim 1
if sel1 is not None and sel1.dtype.kind == 'b':
# assume boolean condition, convert to indices
sel1, = np.nonzero(sel1)
# shortcuts
if sel0 is None and sel1 is None:
return copy(data, blen=blen, storage=storage, create=create, **kwargs)
elif sel1 is None:
return compress(sel0, data, axis=0, blen=blen, storage=storage,
create=create, **kwargs)
elif sel0 is None:
return take(data, sel1, axis=1, blen=blen, storage=storage,
create=create, **kwargs)
# build output
sel0_nnz = count_nonzero(sel0)
out = None
for i in range(0, length, blen):
j = min(i+blen, length)
bsel0 = sel0[i:j]
# don't access data unless we have to
if np.any(bsel0):
block = data[i:j]
res = _numpy_subset(block, bsel0, sel1)
if out is None:
out = getattr(storage, create)(res, expectedlen=sel0_nnz,
**kwargs)
else:
out.append(res)
return out | python | def subset(data, sel0=None, sel1=None, blen=None, storage=None, create='array',
**kwargs):
# TODO refactor sel0 and sel1 normalization with ndarray.subset
# setup
storage = _util.get_storage(storage)
blen = _util.get_blen_array(data, blen)
length = len(data)
if sel0 is not None:
sel0 = np.asanyarray(sel0)
if sel1 is not None:
sel1 = np.asanyarray(sel1)
# ensure boolean array for dim 0
if sel0 is not None and sel0.dtype.kind != 'b':
# assume indices, convert to boolean condition
tmp = np.zeros(length, dtype=bool)
tmp[sel0] = True
sel0 = tmp
# ensure indices for dim 1
if sel1 is not None and sel1.dtype.kind == 'b':
# assume boolean condition, convert to indices
sel1, = np.nonzero(sel1)
# shortcuts
if sel0 is None and sel1 is None:
return copy(data, blen=blen, storage=storage, create=create, **kwargs)
elif sel1 is None:
return compress(sel0, data, axis=0, blen=blen, storage=storage,
create=create, **kwargs)
elif sel0 is None:
return take(data, sel1, axis=1, blen=blen, storage=storage,
create=create, **kwargs)
# build output
sel0_nnz = count_nonzero(sel0)
out = None
for i in range(0, length, blen):
j = min(i+blen, length)
bsel0 = sel0[i:j]
# don't access data unless we have to
if np.any(bsel0):
block = data[i:j]
res = _numpy_subset(block, bsel0, sel1)
if out is None:
out = getattr(storage, create)(res, expectedlen=sel0_nnz,
**kwargs)
else:
out.append(res)
return out | [
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1,010 | cggh/scikit-allel | allel/chunked/core.py | binary_op | def binary_op(data, op, other, blen=None, storage=None, create='array',
**kwargs):
"""Compute a binary operation block-wise over `data`."""
# normalise scalars
if hasattr(other, 'shape') and len(other.shape) == 0:
other = other[()]
if np.isscalar(other):
def f(block):
return op(block, other)
return map_blocks(data, f, blen=blen, storage=storage, create=create, **kwargs)
elif len(data) == len(other):
def f(a, b):
return op(a, b)
return map_blocks((data, other), f, blen=blen, storage=storage, create=create,
**kwargs)
else:
raise NotImplementedError('argument type not supported') | python | def binary_op(data, op, other, blen=None, storage=None, create='array',
**kwargs):
# normalise scalars
if hasattr(other, 'shape') and len(other.shape) == 0:
other = other[()]
if np.isscalar(other):
def f(block):
return op(block, other)
return map_blocks(data, f, blen=blen, storage=storage, create=create, **kwargs)
elif len(data) == len(other):
def f(a, b):
return op(a, b)
return map_blocks((data, other), f, blen=blen, storage=storage, create=create,
**kwargs)
else:
raise NotImplementedError('argument type not supported') | [
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1,011 | cggh/scikit-allel | allel/chunked/core.py | eval_table | def eval_table(tbl, expression, vm='python', blen=None, storage=None,
create='array', vm_kwargs=None, **kwargs):
"""Evaluate `expression` against columns of a table."""
# setup
storage = _util.get_storage(storage)
names, columns = _util.check_table_like(tbl)
length = len(columns[0])
if vm_kwargs is None:
vm_kwargs = dict()
# setup vm
if vm == 'numexpr':
import numexpr
evaluate = numexpr.evaluate
elif vm == 'python':
# noinspection PyUnusedLocal
def evaluate(expr, local_dict=None, **kw):
# takes no keyword arguments
return eval(expr, dict(), local_dict)
else:
raise ValueError('expected vm either "numexpr" or "python"')
# compile expression and get required columns
variables = _get_expression_variables(expression, vm)
required_columns = {v: columns[names.index(v)] for v in variables}
# determine block size for evaluation
blen = _util.get_blen_table(required_columns, blen=blen)
# build output
out = None
for i in range(0, length, blen):
j = min(i+blen, length)
blocals = {v: c[i:j] for v, c in required_columns.items()}
res = evaluate(expression, local_dict=blocals, **vm_kwargs)
if out is None:
out = getattr(storage, create)(res, expectedlen=length, **kwargs)
else:
out.append(res)
return out | python | def eval_table(tbl, expression, vm='python', blen=None, storage=None,
create='array', vm_kwargs=None, **kwargs):
# setup
storage = _util.get_storage(storage)
names, columns = _util.check_table_like(tbl)
length = len(columns[0])
if vm_kwargs is None:
vm_kwargs = dict()
# setup vm
if vm == 'numexpr':
import numexpr
evaluate = numexpr.evaluate
elif vm == 'python':
# noinspection PyUnusedLocal
def evaluate(expr, local_dict=None, **kw):
# takes no keyword arguments
return eval(expr, dict(), local_dict)
else:
raise ValueError('expected vm either "numexpr" or "python"')
# compile expression and get required columns
variables = _get_expression_variables(expression, vm)
required_columns = {v: columns[names.index(v)] for v in variables}
# determine block size for evaluation
blen = _util.get_blen_table(required_columns, blen=blen)
# build output
out = None
for i in range(0, length, blen):
j = min(i+blen, length)
blocals = {v: c[i:j] for v, c in required_columns.items()}
res = evaluate(expression, local_dict=blocals, **vm_kwargs)
if out is None:
out = getattr(storage, create)(res, expectedlen=length, **kwargs)
else:
out.append(res)
return out | [
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1,012 | cggh/scikit-allel | allel/model/util.py | create_allele_mapping | def create_allele_mapping(ref, alt, alleles, dtype='i1'):
"""Create an array mapping variant alleles into a different allele index
system.
Parameters
----------
ref : array_like, S1, shape (n_variants,)
Reference alleles.
alt : array_like, S1, shape (n_variants, n_alt_alleles)
Alternate alleles.
alleles : array_like, S1, shape (n_variants, n_alleles)
Alleles defining the new allele indexing.
dtype : dtype, optional
Output dtype.
Returns
-------
mapping : ndarray, int8, shape (n_variants, n_alt_alleles + 1)
Examples
--------
Example with biallelic variants::
>>> import allel
>>> ref = [b'A', b'C', b'T', b'G']
>>> alt = [b'T', b'G', b'C', b'A']
>>> alleles = [[b'A', b'T'], # no transformation
... [b'G', b'C'], # swap
... [b'T', b'A'], # 1 missing
... [b'A', b'C']] # 1 missing
>>> mapping = allel.create_allele_mapping(ref, alt, alleles)
>>> mapping
array([[ 0, 1],
[ 1, 0],
[ 0, -1],
[-1, 0]], dtype=int8)
Example with multiallelic variants::
>>> ref = [b'A', b'C', b'T']
>>> alt = [[b'T', b'G'],
... [b'A', b'T'],
... [b'G', b'.']]
>>> alleles = [[b'A', b'T'],
... [b'C', b'T'],
... [b'G', b'A']]
>>> mapping = create_allele_mapping(ref, alt, alleles)
>>> mapping
array([[ 0, 1, -1],
[ 0, -1, 1],
[-1, 0, -1]], dtype=int8)
See Also
--------
GenotypeArray.map_alleles, HaplotypeArray.map_alleles, AlleleCountsArray.map_alleles
"""
ref = asarray_ndim(ref, 1)
alt = asarray_ndim(alt, 1, 2)
alleles = asarray_ndim(alleles, 1, 2)
check_dim0_aligned(ref, alt, alleles)
# reshape for convenience
ref = ref[:, None]
if alt.ndim == 1:
alt = alt[:, None]
if alleles.ndim == 1:
alleles = alleles[:, None]
source_alleles = np.append(ref, alt, axis=1)
# setup output array
out = np.empty(source_alleles.shape, dtype=dtype)
out.fill(-1)
# find matches
for ai in range(source_alleles.shape[1]):
match = source_alleles[:, ai, None] == alleles
match_i, match_j = match.nonzero()
out[match_i, ai] = match_j
return out | python | def create_allele_mapping(ref, alt, alleles, dtype='i1'):
ref = asarray_ndim(ref, 1)
alt = asarray_ndim(alt, 1, 2)
alleles = asarray_ndim(alleles, 1, 2)
check_dim0_aligned(ref, alt, alleles)
# reshape for convenience
ref = ref[:, None]
if alt.ndim == 1:
alt = alt[:, None]
if alleles.ndim == 1:
alleles = alleles[:, None]
source_alleles = np.append(ref, alt, axis=1)
# setup output array
out = np.empty(source_alleles.shape, dtype=dtype)
out.fill(-1)
# find matches
for ai in range(source_alleles.shape[1]):
match = source_alleles[:, ai, None] == alleles
match_i, match_j = match.nonzero()
out[match_i, ai] = match_j
return out | [
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system.
Parameters
----------
ref : array_like, S1, shape (n_variants,)
Reference alleles.
alt : array_like, S1, shape (n_variants, n_alt_alleles)
Alternate alleles.
alleles : array_like, S1, shape (n_variants, n_alleles)
Alleles defining the new allele indexing.
dtype : dtype, optional
Output dtype.
Returns
-------
mapping : ndarray, int8, shape (n_variants, n_alt_alleles + 1)
Examples
--------
Example with biallelic variants::
>>> import allel
>>> ref = [b'A', b'C', b'T', b'G']
>>> alt = [b'T', b'G', b'C', b'A']
>>> alleles = [[b'A', b'T'], # no transformation
... [b'G', b'C'], # swap
... [b'T', b'A'], # 1 missing
... [b'A', b'C']] # 1 missing
>>> mapping = allel.create_allele_mapping(ref, alt, alleles)
>>> mapping
array([[ 0, 1],
[ 1, 0],
[ 0, -1],
[-1, 0]], dtype=int8)
Example with multiallelic variants::
>>> ref = [b'A', b'C', b'T']
>>> alt = [[b'T', b'G'],
... [b'A', b'T'],
... [b'G', b'.']]
>>> alleles = [[b'A', b'T'],
... [b'C', b'T'],
... [b'G', b'A']]
>>> mapping = create_allele_mapping(ref, alt, alleles)
>>> mapping
array([[ 0, 1, -1],
[ 0, -1, 1],
[-1, 0, -1]], dtype=int8)
See Also
--------
GenotypeArray.map_alleles, HaplotypeArray.map_alleles, AlleleCountsArray.map_alleles | [
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1,013 | cggh/scikit-allel | allel/model/util.py | locate_fixed_differences | def locate_fixed_differences(ac1, ac2):
"""Locate variants with no shared alleles between two populations.
Parameters
----------
ac1 : array_like, int, shape (n_variants, n_alleles)
Allele counts array from the first population.
ac2 : array_like, int, shape (n_variants, n_alleles)
Allele counts array from the second population.
Returns
-------
loc : ndarray, bool, shape (n_variants,)
See Also
--------
allel.stats.diversity.windowed_df
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 0], [1, 1], [1, 1]],
... [[0, 1], [0, 1], [0, 1], [0, 1]],
... [[0, 1], [0, 1], [1, 1], [1, 1]],
... [[0, 0], [0, 0], [1, 1], [2, 2]],
... [[0, 0], [-1, -1], [1, 1], [-1, -1]]])
>>> ac1 = g.count_alleles(subpop=[0, 1])
>>> ac2 = g.count_alleles(subpop=[2, 3])
>>> loc_df = allel.locate_fixed_differences(ac1, ac2)
>>> loc_df
array([ True, False, False, True, True])
"""
# check inputs
ac1 = asarray_ndim(ac1, 2)
ac2 = asarray_ndim(ac2, 2)
check_dim0_aligned(ac1, ac2)
ac1, ac2 = ensure_dim1_aligned(ac1, ac2)
# stack allele counts for convenience
pac = np.dstack([ac1, ac2])
# count numbers of alleles called in each population
pan = np.sum(pac, axis=1)
# count the numbers of populations with each allele
npa = np.sum(pac > 0, axis=2)
# locate variants with allele calls in both populations
non_missing = np.all(pan > 0, axis=1)
# locate variants where all alleles are only found in a single population
no_shared_alleles = np.all(npa <= 1, axis=1)
return non_missing & no_shared_alleles | python | def locate_fixed_differences(ac1, ac2):
# check inputs
ac1 = asarray_ndim(ac1, 2)
ac2 = asarray_ndim(ac2, 2)
check_dim0_aligned(ac1, ac2)
ac1, ac2 = ensure_dim1_aligned(ac1, ac2)
# stack allele counts for convenience
pac = np.dstack([ac1, ac2])
# count numbers of alleles called in each population
pan = np.sum(pac, axis=1)
# count the numbers of populations with each allele
npa = np.sum(pac > 0, axis=2)
# locate variants with allele calls in both populations
non_missing = np.all(pan > 0, axis=1)
# locate variants where all alleles are only found in a single population
no_shared_alleles = np.all(npa <= 1, axis=1)
return non_missing & no_shared_alleles | [
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Parameters
----------
ac1 : array_like, int, shape (n_variants, n_alleles)
Allele counts array from the first population.
ac2 : array_like, int, shape (n_variants, n_alleles)
Allele counts array from the second population.
Returns
-------
loc : ndarray, bool, shape (n_variants,)
See Also
--------
allel.stats.diversity.windowed_df
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 0], [1, 1], [1, 1]],
... [[0, 1], [0, 1], [0, 1], [0, 1]],
... [[0, 1], [0, 1], [1, 1], [1, 1]],
... [[0, 0], [0, 0], [1, 1], [2, 2]],
... [[0, 0], [-1, -1], [1, 1], [-1, -1]]])
>>> ac1 = g.count_alleles(subpop=[0, 1])
>>> ac2 = g.count_alleles(subpop=[2, 3])
>>> loc_df = allel.locate_fixed_differences(ac1, ac2)
>>> loc_df
array([ True, False, False, True, True]) | [
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1,014 | cggh/scikit-allel | allel/model/util.py | locate_private_alleles | def locate_private_alleles(*acs):
"""Locate alleles that are found only in a single population.
Parameters
----------
*acs : array_like, int, shape (n_variants, n_alleles)
Allele counts arrays from each population.
Returns
-------
loc : ndarray, bool, shape (n_variants, n_alleles)
Boolean array where elements are True if allele is private to a
single population.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 0], [1, 1], [1, 1]],
... [[0, 1], [0, 1], [0, 1], [0, 1]],
... [[0, 1], [0, 1], [1, 1], [1, 1]],
... [[0, 0], [0, 0], [1, 1], [2, 2]],
... [[0, 0], [-1, -1], [1, 1], [-1, -1]]])
>>> ac1 = g.count_alleles(subpop=[0, 1])
>>> ac2 = g.count_alleles(subpop=[2])
>>> ac3 = g.count_alleles(subpop=[3])
>>> loc_private_alleles = allel.locate_private_alleles(ac1, ac2, ac3)
>>> loc_private_alleles
array([[ True, False, False],
[False, False, False],
[ True, False, False],
[ True, True, True],
[ True, True, False]])
>>> loc_private_variants = np.any(loc_private_alleles, axis=1)
>>> loc_private_variants
array([ True, False, True, True, True])
"""
# check inputs
acs = [asarray_ndim(ac, 2) for ac in acs]
check_dim0_aligned(*acs)
acs = ensure_dim1_aligned(*acs)
# stack allele counts for convenience
pac = np.dstack(acs)
# count the numbers of populations with each allele
npa = np.sum(pac > 0, axis=2)
# locate alleles found only in a single population
loc_pa = npa == 1
return loc_pa | python | def locate_private_alleles(*acs):
# check inputs
acs = [asarray_ndim(ac, 2) for ac in acs]
check_dim0_aligned(*acs)
acs = ensure_dim1_aligned(*acs)
# stack allele counts for convenience
pac = np.dstack(acs)
# count the numbers of populations with each allele
npa = np.sum(pac > 0, axis=2)
# locate alleles found only in a single population
loc_pa = npa == 1
return loc_pa | [
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Parameters
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*acs : array_like, int, shape (n_variants, n_alleles)
Allele counts arrays from each population.
Returns
-------
loc : ndarray, bool, shape (n_variants, n_alleles)
Boolean array where elements are True if allele is private to a
single population.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 0], [1, 1], [1, 1]],
... [[0, 1], [0, 1], [0, 1], [0, 1]],
... [[0, 1], [0, 1], [1, 1], [1, 1]],
... [[0, 0], [0, 0], [1, 1], [2, 2]],
... [[0, 0], [-1, -1], [1, 1], [-1, -1]]])
>>> ac1 = g.count_alleles(subpop=[0, 1])
>>> ac2 = g.count_alleles(subpop=[2])
>>> ac3 = g.count_alleles(subpop=[3])
>>> loc_private_alleles = allel.locate_private_alleles(ac1, ac2, ac3)
>>> loc_private_alleles
array([[ True, False, False],
[False, False, False],
[ True, False, False],
[ True, True, True],
[ True, True, False]])
>>> loc_private_variants = np.any(loc_private_alleles, axis=1)
>>> loc_private_variants
array([ True, False, True, True, True]) | [
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1,015 | cggh/scikit-allel | allel/stats/fst.py | patterson_fst | def patterson_fst(aca, acb):
"""Estimator of differentiation between populations A and B based on the
F2 parameter.
Parameters
----------
aca : array_like, int, shape (n_variants, 2)
Allele counts for population A.
acb : array_like, int, shape (n_variants, 2)
Allele counts for population B.
Returns
-------
num : ndarray, shape (n_variants,), float
Numerator.
den : ndarray, shape (n_variants,), float
Denominator.
Notes
-----
See Patterson (2012), Appendix A.
TODO check if this is numerically equivalent to Hudson's estimator.
"""
from allel.stats.admixture import patterson_f2, h_hat
num = patterson_f2(aca, acb)
den = num + h_hat(aca) + h_hat(acb)
return num, den | python | def patterson_fst(aca, acb):
from allel.stats.admixture import patterson_f2, h_hat
num = patterson_f2(aca, acb)
den = num + h_hat(aca) + h_hat(acb)
return num, den | [
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Parameters
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aca : array_like, int, shape (n_variants, 2)
Allele counts for population A.
acb : array_like, int, shape (n_variants, 2)
Allele counts for population B.
Returns
-------
num : ndarray, shape (n_variants,), float
Numerator.
den : ndarray, shape (n_variants,), float
Denominator.
Notes
-----
See Patterson (2012), Appendix A.
TODO check if this is numerically equivalent to Hudson's estimator. | [
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1,016 | cggh/scikit-allel | allel/stats/fst.py | average_weir_cockerham_fst | def average_weir_cockerham_fst(g, subpops, blen, max_allele=None):
"""Estimate average Fst and standard error using the block-jackknife.
Parameters
----------
g : array_like, int, shape (n_variants, n_samples, ploidy)
Genotype array.
subpops : sequence of sequences of ints
Sample indices for each subpopulation.
blen : int
Block size (number of variants).
max_allele : int, optional
The highest allele index to consider.
Returns
-------
fst : float
Estimated value of the statistic using all data.
se : float
Estimated standard error.
vb : ndarray, float, shape (n_blocks,)
Value of the statistic in each block.
vj : ndarray, float, shape (n_blocks,)
Values of the statistic from block-jackknife resampling.
"""
# calculate per-variant values
a, b, c = weir_cockerham_fst(g, subpops, max_allele=max_allele)
# calculate overall estimate
a_sum = np.nansum(a)
b_sum = np.nansum(b)
c_sum = np.nansum(c)
fst = a_sum / (a_sum + b_sum + c_sum)
# compute the numerator and denominator within each block
num_bsum = moving_statistic(a, statistic=np.nansum, size=blen)
den_bsum = moving_statistic(a + b + c, statistic=np.nansum, size=blen)
# calculate the statistic values in each block
vb = num_bsum / den_bsum
# estimate standard error
_, se, vj = jackknife((num_bsum, den_bsum),
statistic=lambda n, d: np.sum(n) / np.sum(d))
return fst, se, vb, vj | python | def average_weir_cockerham_fst(g, subpops, blen, max_allele=None):
# calculate per-variant values
a, b, c = weir_cockerham_fst(g, subpops, max_allele=max_allele)
# calculate overall estimate
a_sum = np.nansum(a)
b_sum = np.nansum(b)
c_sum = np.nansum(c)
fst = a_sum / (a_sum + b_sum + c_sum)
# compute the numerator and denominator within each block
num_bsum = moving_statistic(a, statistic=np.nansum, size=blen)
den_bsum = moving_statistic(a + b + c, statistic=np.nansum, size=blen)
# calculate the statistic values in each block
vb = num_bsum / den_bsum
# estimate standard error
_, se, vj = jackknife((num_bsum, den_bsum),
statistic=lambda n, d: np.sum(n) / np.sum(d))
return fst, se, vb, vj | [
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Parameters
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g : array_like, int, shape (n_variants, n_samples, ploidy)
Genotype array.
subpops : sequence of sequences of ints
Sample indices for each subpopulation.
blen : int
Block size (number of variants).
max_allele : int, optional
The highest allele index to consider.
Returns
-------
fst : float
Estimated value of the statistic using all data.
se : float
Estimated standard error.
vb : ndarray, float, shape (n_blocks,)
Value of the statistic in each block.
vj : ndarray, float, shape (n_blocks,)
Values of the statistic from block-jackknife resampling. | [
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1,017 | cggh/scikit-allel | allel/stats/ld.py | plot_pairwise_ld | def plot_pairwise_ld(m, colorbar=True, ax=None, imshow_kwargs=None):
"""Plot a matrix of genotype linkage disequilibrium values between
all pairs of variants.
Parameters
----------
m : array_like
Array of linkage disequilibrium values in condensed form.
colorbar : bool, optional
If True, add a colorbar to the current figure.
ax : axes, optional
The axes on which to draw. If not provided, a new figure will be
created.
imshow_kwargs : dict-like, optional
Additional keyword arguments passed through to
:func:`matplotlib.pyplot.imshow`.
Returns
-------
ax : axes
The axes on which the plot was drawn.
"""
import matplotlib.pyplot as plt
# check inputs
m_square = ensure_square(m)
# blank out lower triangle and flip up/down
m_square = np.tril(m_square)[::-1, :]
# set up axes
if ax is None:
# make a square figure with enough pixels to represent each variant
x = m_square.shape[0] / plt.rcParams['figure.dpi']
x = max(x, plt.rcParams['figure.figsize'][0])
fig, ax = plt.subplots(figsize=(x, x))
fig.tight_layout(pad=0)
# setup imshow arguments
if imshow_kwargs is None:
imshow_kwargs = dict()
imshow_kwargs.setdefault('interpolation', 'none')
imshow_kwargs.setdefault('cmap', 'Greys')
imshow_kwargs.setdefault('vmin', 0)
imshow_kwargs.setdefault('vmax', 1)
# plot as image
im = ax.imshow(m_square, **imshow_kwargs)
# tidy up
ax.set_xticks([])
ax.set_yticks([])
for s in 'bottom', 'right':
ax.spines[s].set_visible(False)
if colorbar:
plt.gcf().colorbar(im, shrink=.5, pad=0)
return ax | python | def plot_pairwise_ld(m, colorbar=True, ax=None, imshow_kwargs=None):
import matplotlib.pyplot as plt
# check inputs
m_square = ensure_square(m)
# blank out lower triangle and flip up/down
m_square = np.tril(m_square)[::-1, :]
# set up axes
if ax is None:
# make a square figure with enough pixels to represent each variant
x = m_square.shape[0] / plt.rcParams['figure.dpi']
x = max(x, plt.rcParams['figure.figsize'][0])
fig, ax = plt.subplots(figsize=(x, x))
fig.tight_layout(pad=0)
# setup imshow arguments
if imshow_kwargs is None:
imshow_kwargs = dict()
imshow_kwargs.setdefault('interpolation', 'none')
imshow_kwargs.setdefault('cmap', 'Greys')
imshow_kwargs.setdefault('vmin', 0)
imshow_kwargs.setdefault('vmax', 1)
# plot as image
im = ax.imshow(m_square, **imshow_kwargs)
# tidy up
ax.set_xticks([])
ax.set_yticks([])
for s in 'bottom', 'right':
ax.spines[s].set_visible(False)
if colorbar:
plt.gcf().colorbar(im, shrink=.5, pad=0)
return ax | [
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Parameters
----------
m : array_like
Array of linkage disequilibrium values in condensed form.
colorbar : bool, optional
If True, add a colorbar to the current figure.
ax : axes, optional
The axes on which to draw. If not provided, a new figure will be
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imshow_kwargs : dict-like, optional
Additional keyword arguments passed through to
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Returns
-------
ax : axes
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1,018 | cggh/scikit-allel | allel/io/util.py | array_to_hdf5 | def array_to_hdf5(a, parent, name, **kwargs):
"""Write a Numpy array to an HDF5 dataset.
Parameters
----------
a : ndarray
Data to write.
parent : string or h5py group
Parent HDF5 file or group. If a string, will be treated as HDF5 file
name.
name : string
Name or path of dataset to write data into.
kwargs : keyword arguments
Passed through to h5py require_dataset() function.
Returns
-------
h5d : h5py dataset
"""
import h5py
h5f = None
if isinstance(parent, str):
h5f = h5py.File(parent, mode='a')
parent = h5f
try:
kwargs.setdefault('chunks', True) # auto-chunking
kwargs.setdefault('dtype', a.dtype)
kwargs.setdefault('compression', 'gzip')
h5d = parent.require_dataset(name, shape=a.shape, **kwargs)
h5d[...] = a
return h5d
finally:
if h5f is not None:
h5f.close() | python | def array_to_hdf5(a, parent, name, **kwargs):
import h5py
h5f = None
if isinstance(parent, str):
h5f = h5py.File(parent, mode='a')
parent = h5f
try:
kwargs.setdefault('chunks', True) # auto-chunking
kwargs.setdefault('dtype', a.dtype)
kwargs.setdefault('compression', 'gzip')
h5d = parent.require_dataset(name, shape=a.shape, **kwargs)
h5d[...] = a
return h5d
finally:
if h5f is not None:
h5f.close() | [
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Parameters
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Data to write.
parent : string or h5py group
Parent HDF5 file or group. If a string, will be treated as HDF5 file
name.
name : string
Name or path of dataset to write data into.
kwargs : keyword arguments
Passed through to h5py require_dataset() function.
Returns
-------
h5d : h5py dataset | [
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1,019 | cggh/scikit-allel | allel/io/util.py | recarray_from_hdf5_group | def recarray_from_hdf5_group(*args, **kwargs):
"""Load a recarray from columns stored as separate datasets with an
HDF5 group.
Either provide an h5py group as a single positional argument,
or provide two positional arguments giving the HDF5 file path and the
group node path within the file.
The following optional parameters may be given.
Parameters
----------
start : int, optional
Index to start loading from.
stop : int, optional
Index to finish loading at.
condition : array_like, bool, optional
A 1-dimensional boolean array of the same length as the columns of the
table to load, indicating a selection of rows to load.
"""
import h5py
h5f = None
if len(args) == 1:
group = args[0]
elif len(args) == 2:
file_path, node_path = args
h5f = h5py.File(file_path, mode='r')
try:
group = h5f[node_path]
except Exception as e:
h5f.close()
raise e
else:
raise ValueError('bad arguments; expected group or (file_path, '
'node_path), found %s' % repr(args))
try:
if not isinstance(group, h5py.Group):
raise ValueError('expected group, found %r' % group)
# determine dataset names to load
available_dataset_names = [n for n in group.keys()
if isinstance(group[n], h5py.Dataset)]
names = kwargs.pop('names', available_dataset_names)
names = [str(n) for n in names] # needed for PY2
for n in names:
if n not in set(group.keys()):
raise ValueError('name not found: %s' % n)
if not isinstance(group[n], h5py.Dataset):
raise ValueError('name does not refer to a dataset: %s, %r'
% (n, group[n]))
# check datasets are aligned
datasets = [group[n] for n in names]
length = datasets[0].shape[0]
for d in datasets[1:]:
if d.shape[0] != length:
raise ValueError('datasets must be of equal length')
# determine start and stop parameters for load
start = kwargs.pop('start', 0)
stop = kwargs.pop('stop', length)
# check condition
condition = kwargs.pop('condition', None) # type: np.ndarray
condition = asarray_ndim(condition, 1, allow_none=True)
if condition is not None and condition.size != length:
raise ValueError('length of condition does not match length '
'of datasets')
# setup output data
dtype = [(n, d.dtype, d.shape[1:]) for n, d in zip(names, datasets)]
ra = np.empty(length, dtype=dtype)
for n, d in zip(names, datasets):
a = d[start:stop]
if condition is not None:
a = np.compress(condition[start:stop], a, axis=0)
ra[n] = a
return ra
finally:
if h5f is not None:
h5f.close() | python | def recarray_from_hdf5_group(*args, **kwargs):
import h5py
h5f = None
if len(args) == 1:
group = args[0]
elif len(args) == 2:
file_path, node_path = args
h5f = h5py.File(file_path, mode='r')
try:
group = h5f[node_path]
except Exception as e:
h5f.close()
raise e
else:
raise ValueError('bad arguments; expected group or (file_path, '
'node_path), found %s' % repr(args))
try:
if not isinstance(group, h5py.Group):
raise ValueError('expected group, found %r' % group)
# determine dataset names to load
available_dataset_names = [n for n in group.keys()
if isinstance(group[n], h5py.Dataset)]
names = kwargs.pop('names', available_dataset_names)
names = [str(n) for n in names] # needed for PY2
for n in names:
if n not in set(group.keys()):
raise ValueError('name not found: %s' % n)
if not isinstance(group[n], h5py.Dataset):
raise ValueError('name does not refer to a dataset: %s, %r'
% (n, group[n]))
# check datasets are aligned
datasets = [group[n] for n in names]
length = datasets[0].shape[0]
for d in datasets[1:]:
if d.shape[0] != length:
raise ValueError('datasets must be of equal length')
# determine start and stop parameters for load
start = kwargs.pop('start', 0)
stop = kwargs.pop('stop', length)
# check condition
condition = kwargs.pop('condition', None) # type: np.ndarray
condition = asarray_ndim(condition, 1, allow_none=True)
if condition is not None and condition.size != length:
raise ValueError('length of condition does not match length '
'of datasets')
# setup output data
dtype = [(n, d.dtype, d.shape[1:]) for n, d in zip(names, datasets)]
ra = np.empty(length, dtype=dtype)
for n, d in zip(names, datasets):
a = d[start:stop]
if condition is not None:
a = np.compress(condition[start:stop], a, axis=0)
ra[n] = a
return ra
finally:
if h5f is not None:
h5f.close() | [
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Either provide an h5py group as a single positional argument,
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The following optional parameters may be given.
Parameters
----------
start : int, optional
Index to start loading from.
stop : int, optional
Index to finish loading at.
condition : array_like, bool, optional
A 1-dimensional boolean array of the same length as the columns of the
table to load, indicating a selection of rows to load. | [
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1,020 | cggh/scikit-allel | allel/io/util.py | recarray_to_hdf5_group | def recarray_to_hdf5_group(ra, parent, name, **kwargs):
"""Write each column in a recarray to a dataset in an HDF5 group.
Parameters
----------
ra : recarray
Numpy recarray to store.
parent : string or h5py group
Parent HDF5 file or group. If a string, will be treated as HDF5 file
name.
name : string
Name or path of group to write data into.
kwargs : keyword arguments
Passed through to h5py require_dataset() function.
Returns
-------
h5g : h5py group
"""
import h5py
h5f = None
if isinstance(parent, str):
h5f = h5py.File(parent, mode='a')
parent = h5f
try:
h5g = parent.require_group(name)
for n in ra.dtype.names:
array_to_hdf5(ra[n], h5g, n, **kwargs)
return h5g
finally:
if h5f is not None:
h5f.close() | python | def recarray_to_hdf5_group(ra, parent, name, **kwargs):
import h5py
h5f = None
if isinstance(parent, str):
h5f = h5py.File(parent, mode='a')
parent = h5f
try:
h5g = parent.require_group(name)
for n in ra.dtype.names:
array_to_hdf5(ra[n], h5g, n, **kwargs)
return h5g
finally:
if h5f is not None:
h5f.close() | [
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1,021 | cggh/scikit-allel | allel/model/ndarray.py | subset | def subset(data, sel0, sel1):
"""Apply selections on first and second axes."""
# check inputs
data = np.asarray(data)
if data.ndim < 2:
raise ValueError('data must have 2 or more dimensions')
sel0 = asarray_ndim(sel0, 1, allow_none=True)
sel1 = asarray_ndim(sel1, 1, allow_none=True)
# ensure indices
if sel0 is not None and sel0.dtype.kind == 'b':
sel0, = np.nonzero(sel0)
if sel1 is not None and sel1.dtype.kind == 'b':
sel1, = np.nonzero(sel1)
# ensure leading dimension indices can be broadcast correctly
if sel0 is not None and sel1 is not None:
sel0 = sel0[:, np.newaxis]
# deal with None arguments
if sel0 is None:
sel0 = _total_slice
if sel1 is None:
sel1 = _total_slice
return data[sel0, sel1] | python | def subset(data, sel0, sel1):
# check inputs
data = np.asarray(data)
if data.ndim < 2:
raise ValueError('data must have 2 or more dimensions')
sel0 = asarray_ndim(sel0, 1, allow_none=True)
sel1 = asarray_ndim(sel1, 1, allow_none=True)
# ensure indices
if sel0 is not None and sel0.dtype.kind == 'b':
sel0, = np.nonzero(sel0)
if sel1 is not None and sel1.dtype.kind == 'b':
sel1, = np.nonzero(sel1)
# ensure leading dimension indices can be broadcast correctly
if sel0 is not None and sel1 is not None:
sel0 = sel0[:, np.newaxis]
# deal with None arguments
if sel0 is None:
sel0 = _total_slice
if sel1 is None:
sel1 = _total_slice
return data[sel0, sel1] | [
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1,022 | cggh/scikit-allel | allel/model/ndarray.py | NumpyRecArrayWrapper.eval | def eval(self, expression, vm='python'):
"""Evaluate an expression against the table columns.
Parameters
----------
expression : string
Expression to evaluate.
vm : {'numexpr', 'python'}
Virtual machine to use.
Returns
-------
result : ndarray
"""
if vm == 'numexpr':
import numexpr as ne
return ne.evaluate(expression, local_dict=self)
else:
if PY2:
# locals must be a mapping
m = {k: self[k] for k in self.dtype.names}
else:
m = self
return eval(expression, dict(), m) | python | def eval(self, expression, vm='python'):
if vm == 'numexpr':
import numexpr as ne
return ne.evaluate(expression, local_dict=self)
else:
if PY2:
# locals must be a mapping
m = {k: self[k] for k in self.dtype.names}
else:
m = self
return eval(expression, dict(), m) | [
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-------
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1,023 | cggh/scikit-allel | allel/model/ndarray.py | NumpyRecArrayWrapper.query | def query(self, expression, vm='python'):
"""Evaluate expression and then use it to extract rows from the table.
Parameters
----------
expression : string
Expression to evaluate.
vm : {'numexpr', 'python'}
Virtual machine to use.
Returns
-------
result : structured array
"""
condition = self.eval(expression, vm=vm)
return self.compress(condition) | python | def query(self, expression, vm='python'):
condition = self.eval(expression, vm=vm)
return self.compress(condition) | [
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1,024 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.fill_masked | def fill_masked(self, value=-1, copy=True):
"""Fill masked genotype calls with a given value.
Parameters
----------
value : int, optional
The fill value.
copy : bool, optional
If False, modify the array in place.
Returns
-------
g : GenotypeArray
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 1], [1, 1]],
... [[0, 2], [-1, -1]]], dtype='i1')
>>> mask = [[True, False], [False, True], [False, False]]
>>> g.mask = mask
>>> g.fill_masked().values
array([[[-1, -1],
[ 0, 1]],
[[ 0, 1],
[-1, -1]],
[[ 0, 2],
[-1, -1]]], dtype=int8)
"""
if self.mask is None:
raise ValueError('no mask is set')
# apply the mask
data = np.array(self.values, copy=copy)
data[self.mask, ...] = value
if copy:
out = type(self)(data) # wrap
out.is_phased = self.is_phased
# don't set mask because it has been filled in
else:
out = self
out.mask = None # reset mask
return out | python | def fill_masked(self, value=-1, copy=True):
if self.mask is None:
raise ValueError('no mask is set')
# apply the mask
data = np.array(self.values, copy=copy)
data[self.mask, ...] = value
if copy:
out = type(self)(data) # wrap
out.is_phased = self.is_phased
# don't set mask because it has been filled in
else:
out = self
out.mask = None # reset mask
return out | [
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Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
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... [[0, 2], [-1, -1]]], dtype='i1')
>>> mask = [[True, False], [False, True], [False, False]]
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1,025 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.is_called | def is_called(self):
"""Find non-missing genotype calls.
Returns
-------
out : ndarray, bool, shape (n_variants, n_samples)
Array where elements are True if the genotype call matches the
condition.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 1], [1, 1]],
... [[0, 2], [-1, -1]]])
>>> g.is_called()
array([[ True, True],
[ True, True],
[ True, False]])
>>> v = g[:, 1]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/1 1/1 ./.
>>> v.is_called()
array([ True, True, False])
"""
out = np.all(self.values >= 0, axis=-1)
# handle mask
if self.mask is not None:
out &= ~self.mask
return out | python | def is_called(self):
out = np.all(self.values >= 0, axis=-1)
# handle mask
if self.mask is not None:
out &= ~self.mask
return out | [
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Returns
-------
out : ndarray, bool, shape (n_variants, n_samples)
Array where elements are True if the genotype call matches the
condition.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 1], [1, 1]],
... [[0, 2], [-1, -1]]])
>>> g.is_called()
array([[ True, True],
[ True, True],
[ True, False]])
>>> v = g[:, 1]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/1 1/1 ./.
>>> v.is_called()
array([ True, True, False]) | [
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1,026 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.is_missing | def is_missing(self):
"""Find missing genotype calls.
Returns
-------
out : ndarray, bool, shape (n_variants, n_samples)
Array where elements are True if the genotype call matches the
condition.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 1], [1, 1]],
... [[0, 2], [-1, -1]]])
>>> g.is_missing()
array([[False, False],
[False, False],
[False, True]])
>>> v = g[:, 1]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/1 1/1 ./.
>>> v.is_missing()
array([False, False, True])
"""
out = np.any(self.values < 0, axis=-1)
# handle mask
if self.mask is not None:
out |= self.mask
return out | python | def is_missing(self):
out = np.any(self.values < 0, axis=-1)
# handle mask
if self.mask is not None:
out |= self.mask
return out | [
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Returns
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out : ndarray, bool, shape (n_variants, n_samples)
Array where elements are True if the genotype call matches the
condition.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 1], [1, 1]],
... [[0, 2], [-1, -1]]])
>>> g.is_missing()
array([[False, False],
[False, False],
[False, True]])
>>> v = g[:, 1]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/1 1/1 ./.
>>> v.is_missing()
array([False, False, True]) | [
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1,027 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.is_hom | def is_hom(self, allele=None):
"""Find genotype calls that are homozygous.
Parameters
----------
allele : int, optional
Allele index.
Returns
-------
out : ndarray, bool, shape (n_variants, n_samples)
Array where elements are True if the genotype call matches the
condition.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 1], [1, 1]],
... [[2, 2], [-1, -1]]])
>>> g.is_hom()
array([[ True, False],
[False, True],
[ True, False]])
>>> g.is_hom(allele=1)
array([[False, False],
[False, True],
[False, False]])
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/0 0/1 2/2
>>> v.is_hom()
array([ True, False, True])
"""
if allele is None:
allele1 = self.values[..., 0, np.newaxis]
other_alleles = self.values[..., 1:]
tmp = (allele1 >= 0) & (allele1 == other_alleles)
out = np.all(tmp, axis=-1)
else:
out = np.all(self.values == allele, axis=-1)
# handle mask
if self.mask is not None:
out &= ~self.mask
return out | python | def is_hom(self, allele=None):
if allele is None:
allele1 = self.values[..., 0, np.newaxis]
other_alleles = self.values[..., 1:]
tmp = (allele1 >= 0) & (allele1 == other_alleles)
out = np.all(tmp, axis=-1)
else:
out = np.all(self.values == allele, axis=-1)
# handle mask
if self.mask is not None:
out &= ~self.mask
return out | [
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Parameters
----------
allele : int, optional
Allele index.
Returns
-------
out : ndarray, bool, shape (n_variants, n_samples)
Array where elements are True if the genotype call matches the
condition.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 1], [1, 1]],
... [[2, 2], [-1, -1]]])
>>> g.is_hom()
array([[ True, False],
[False, True],
[ True, False]])
>>> g.is_hom(allele=1)
array([[False, False],
[False, True],
[False, False]])
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/0 0/1 2/2
>>> v.is_hom()
array([ True, False, True]) | [
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] | 3c979a57a100240ba959dd13f98839349530f215 | https://github.com/cggh/scikit-allel/blob/3c979a57a100240ba959dd13f98839349530f215/allel/model/ndarray.py#L456-L506 |
1,028 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.is_het | def is_het(self, allele=None):
"""Find genotype calls that are heterozygous.
Returns
-------
out : ndarray, bool, shape (n_variants, n_samples)
Array where elements are True if the genotype call matches the
condition.
allele : int, optional
Heterozygous allele.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 1], [1, 1]],
... [[0, 2], [-1, -1]]])
>>> g.is_het()
array([[False, True],
[ True, False],
[ True, False]])
>>> g.is_het(2)
array([[False, False],
[False, False],
[ True, False]])
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/0 0/1 0/2
>>> v.is_het()
array([False, True, True])
"""
allele1 = self.values[..., 0, np.newaxis] # type: np.ndarray
other_alleles = self.values[..., 1:] # type: np.ndarray
out = np.all(self.values >= 0, axis=-1) & np.any(allele1 != other_alleles, axis=-1)
if allele is not None:
out &= np.any(self.values == allele, axis=-1)
# handle mask
if self.mask is not None:
out &= ~self.mask
return out | python | def is_het(self, allele=None):
allele1 = self.values[..., 0, np.newaxis] # type: np.ndarray
other_alleles = self.values[..., 1:] # type: np.ndarray
out = np.all(self.values >= 0, axis=-1) & np.any(allele1 != other_alleles, axis=-1)
if allele is not None:
out &= np.any(self.values == allele, axis=-1)
# handle mask
if self.mask is not None:
out &= ~self.mask
return out | [
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Returns
-------
out : ndarray, bool, shape (n_variants, n_samples)
Array where elements are True if the genotype call matches the
condition.
allele : int, optional
Heterozygous allele.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 1], [1, 1]],
... [[0, 2], [-1, -1]]])
>>> g.is_het()
array([[False, True],
[ True, False],
[ True, False]])
>>> g.is_het(2)
array([[False, False],
[False, False],
[ True, False]])
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/0 0/1 0/2
>>> v.is_het()
array([False, True, True]) | [
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] | 3c979a57a100240ba959dd13f98839349530f215 | https://github.com/cggh/scikit-allel/blob/3c979a57a100240ba959dd13f98839349530f215/allel/model/ndarray.py#L580-L625 |
1,029 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.is_call | def is_call(self, call):
"""Locate genotypes with a given call.
Parameters
----------
call : array_like, int, shape (ploidy,)
The genotype call to find.
Returns
-------
out : ndarray, bool, shape (n_variants, n_samples)
Array where elements are True if the genotype is `call`.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 1], [1, 1]],
... [[0, 2], [-1, -1]]])
>>> g.is_call((0, 2))
array([[False, False],
[False, False],
[ True, False]])
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/0 0/1 0/2
>>> v.is_call((0, 2))
array([False, False, True])
"""
# guard conditions
if not len(call) == self.shape[-1]:
raise ValueError('invalid call ploidy: %s', repr(call))
if self.ndim == 2:
call = np.asarray(call)[np.newaxis, :]
else:
call = np.asarray(call)[np.newaxis, np.newaxis, :]
out = np.all(self.values == call, axis=-1)
# handle mask
if self.mask is not None:
out &= ~self.mask
return out | python | def is_call(self, call):
# guard conditions
if not len(call) == self.shape[-1]:
raise ValueError('invalid call ploidy: %s', repr(call))
if self.ndim == 2:
call = np.asarray(call)[np.newaxis, :]
else:
call = np.asarray(call)[np.newaxis, np.newaxis, :]
out = np.all(self.values == call, axis=-1)
# handle mask
if self.mask is not None:
out &= ~self.mask
return out | [
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Parameters
----------
call : array_like, int, shape (ploidy,)
The genotype call to find.
Returns
-------
out : ndarray, bool, shape (n_variants, n_samples)
Array where elements are True if the genotype is `call`.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 1], [1, 1]],
... [[0, 2], [-1, -1]]])
>>> g.is_call((0, 2))
array([[False, False],
[False, False],
[ True, False]])
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/0 0/1 0/2
>>> v.is_call((0, 2))
array([False, False, True]) | [
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1,030 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.count_called | def count_called(self, axis=None):
"""Count called genotypes.
Parameters
----------
axis : int, optional
Axis over which to count, or None to perform overall count.
"""
b = self.is_called()
return np.sum(b, axis=axis) | python | def count_called(self, axis=None):
b = self.is_called()
return np.sum(b, axis=axis) | [
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----------
axis : int, optional
Axis over which to count, or None to perform overall count. | [
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1,031 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.count_missing | def count_missing(self, axis=None):
"""Count missing genotypes.
Parameters
----------
axis : int, optional
Axis over which to count, or None to perform overall count.
"""
b = self.is_missing()
return np.sum(b, axis=axis) | python | def count_missing(self, axis=None):
b = self.is_missing()
return np.sum(b, axis=axis) | [
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Axis over which to count, or None to perform overall count. | [
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1,032 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.count_hom | def count_hom(self, allele=None, axis=None):
"""Count homozygous genotypes.
Parameters
----------
allele : int, optional
Allele index.
axis : int, optional
Axis over which to count, or None to perform overall count.
"""
b = self.is_hom(allele=allele)
return np.sum(b, axis=axis) | python | def count_hom(self, allele=None, axis=None):
b = self.is_hom(allele=allele)
return np.sum(b, axis=axis) | [
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Allele index.
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Axis over which to count, or None to perform overall count. | [
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1,033 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.count_hom_ref | def count_hom_ref(self, axis=None):
"""Count homozygous reference genotypes.
Parameters
----------
axis : int, optional
Axis over which to count, or None to perform overall count.
"""
b = self.is_hom_ref()
return np.sum(b, axis=axis) | python | def count_hom_ref(self, axis=None):
b = self.is_hom_ref()
return np.sum(b, axis=axis) | [
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1,034 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.count_hom_alt | def count_hom_alt(self, axis=None):
"""Count homozygous alternate genotypes.
Parameters
----------
axis : int, optional
Axis over which to count, or None to perform overall count.
"""
b = self.is_hom_alt()
return np.sum(b, axis=axis) | python | def count_hom_alt(self, axis=None):
b = self.is_hom_alt()
return np.sum(b, axis=axis) | [
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Axis over which to count, or None to perform overall count. | [
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] | 3c979a57a100240ba959dd13f98839349530f215 | https://github.com/cggh/scikit-allel/blob/3c979a57a100240ba959dd13f98839349530f215/allel/model/ndarray.py#L726-L736 |
1,035 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.count_het | def count_het(self, allele=None, axis=None):
"""Count heterozygous genotypes.
Parameters
----------
allele : int, optional
Allele index.
axis : int, optional
Axis over which to count, or None to perform overall count.
"""
b = self.is_het(allele=allele)
return np.sum(b, axis=axis) | python | def count_het(self, allele=None, axis=None):
b = self.is_het(allele=allele)
return np.sum(b, axis=axis) | [
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Parameters
----------
allele : int, optional
Allele index.
axis : int, optional
Axis over which to count, or None to perform overall count. | [
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1,036 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.count_call | def count_call(self, call, axis=None):
"""Count genotypes with a given call.
Parameters
----------
call : array_like, int, shape (ploidy,)
The genotype call to find.
axis : int, optional
Axis over which to count, or None to perform overall count.
"""
b = self.is_call(call=call)
return np.sum(b, axis=axis) | python | def count_call(self, call, axis=None):
b = self.is_call(call=call)
return np.sum(b, axis=axis) | [
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Parameters
----------
call : array_like, int, shape (ploidy,)
The genotype call to find.
axis : int, optional
Axis over which to count, or None to perform overall count. | [
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1,037 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.to_n_ref | def to_n_ref(self, fill=0, dtype='i1'):
"""Transform each genotype call into the number of
reference alleles.
Parameters
----------
fill : int, optional
Use this value to represent missing calls.
dtype : dtype, optional
Output dtype.
Returns
-------
out : ndarray, int8, shape (n_variants, n_samples)
Array of ref alleles per genotype call.
Notes
-----
By default this function returns 0 for missing genotype calls
**and** for homozygous non-reference genotype calls. Use the
`fill` argument to change how missing calls are represented.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[2, 2], [-1, -1]]])
>>> g.to_n_ref()
array([[2, 1],
[1, 0],
[0, 0]], dtype=int8)
>>> g.to_n_ref(fill=-1)
array([[ 2, 1],
[ 1, 0],
[ 0, -1]], dtype=int8)
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/0 0/2 2/2
>>> v.to_n_ref()
array([2, 1, 0], dtype=int8)
"""
# count number of alternate alleles
out = np.empty(self.shape[:-1], dtype=dtype)
np.sum(self.values == 0, axis=-1, out=out)
# fill missing calls
if fill != 0:
m = self.is_missing()
out[m] = fill
# handle mask
if self.mask is not None:
out[self.mask] = fill
return out | python | def to_n_ref(self, fill=0, dtype='i1'):
# count number of alternate alleles
out = np.empty(self.shape[:-1], dtype=dtype)
np.sum(self.values == 0, axis=-1, out=out)
# fill missing calls
if fill != 0:
m = self.is_missing()
out[m] = fill
# handle mask
if self.mask is not None:
out[self.mask] = fill
return out | [
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reference alleles.
Parameters
----------
fill : int, optional
Use this value to represent missing calls.
dtype : dtype, optional
Output dtype.
Returns
-------
out : ndarray, int8, shape (n_variants, n_samples)
Array of ref alleles per genotype call.
Notes
-----
By default this function returns 0 for missing genotype calls
**and** for homozygous non-reference genotype calls. Use the
`fill` argument to change how missing calls are represented.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[2, 2], [-1, -1]]])
>>> g.to_n_ref()
array([[2, 1],
[1, 0],
[0, 0]], dtype=int8)
>>> g.to_n_ref(fill=-1)
array([[ 2, 1],
[ 1, 0],
[ 0, -1]], dtype=int8)
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/0 0/2 2/2
>>> v.to_n_ref()
array([2, 1, 0], dtype=int8) | [
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1,038 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.to_allele_counts | def to_allele_counts(self, max_allele=None, dtype='u1'):
"""Transform genotype calls into allele counts per call.
Parameters
----------
max_allele : int, optional
Highest allele index. Provide this value to speed up computation.
dtype : dtype, optional
Output dtype.
Returns
-------
out : ndarray, uint8, shape (n_variants, n_samples, len(alleles))
Array of allele counts per call.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[2, 2], [-1, -1]]])
>>> g.to_allele_counts()
<GenotypeAlleleCountsArray shape=(3, 2, 3) dtype=uint8>
2:0:0 1:1:0
1:0:1 0:2:0
0:0:2 0:0:0
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/0 0/2 2/2
>>> v.to_allele_counts()
<GenotypeAlleleCountsVector shape=(3, 3) dtype=uint8>
2:0:0 1:0:1 0:0:2
"""
# determine alleles to count
if max_allele is None:
max_allele = self.max()
alleles = list(range(max_allele + 1))
# set up output array
outshape = self.shape[:-1] + (len(alleles),)
out = np.zeros(outshape, dtype=dtype)
for allele in alleles:
# count alleles along ploidy dimension
allele_match = self.values == allele
if self.mask is not None:
allele_match &= ~self.mask[..., np.newaxis]
np.sum(allele_match, axis=-1, out=out[..., allele])
if self.ndim == 2:
out = GenotypeAlleleCountsVector(out)
elif self.ndim == 3:
out = GenotypeAlleleCountsArray(out)
return out | python | def to_allele_counts(self, max_allele=None, dtype='u1'):
# determine alleles to count
if max_allele is None:
max_allele = self.max()
alleles = list(range(max_allele + 1))
# set up output array
outshape = self.shape[:-1] + (len(alleles),)
out = np.zeros(outshape, dtype=dtype)
for allele in alleles:
# count alleles along ploidy dimension
allele_match = self.values == allele
if self.mask is not None:
allele_match &= ~self.mask[..., np.newaxis]
np.sum(allele_match, axis=-1, out=out[..., allele])
if self.ndim == 2:
out = GenotypeAlleleCountsVector(out)
elif self.ndim == 3:
out = GenotypeAlleleCountsArray(out)
return out | [
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Parameters
----------
max_allele : int, optional
Highest allele index. Provide this value to speed up computation.
dtype : dtype, optional
Output dtype.
Returns
-------
out : ndarray, uint8, shape (n_variants, n_samples, len(alleles))
Array of allele counts per call.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[2, 2], [-1, -1]]])
>>> g.to_allele_counts()
<GenotypeAlleleCountsArray shape=(3, 2, 3) dtype=uint8>
2:0:0 1:1:0
1:0:1 0:2:0
0:0:2 0:0:0
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(3, 2) dtype=int64>
0/0 0/2 2/2
>>> v.to_allele_counts()
<GenotypeAlleleCountsVector shape=(3, 3) dtype=uint8>
2:0:0 1:0:1 0:0:2 | [
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1,039 | cggh/scikit-allel | allel/model/ndarray.py | Genotypes.to_gt | def to_gt(self, max_allele=None):
"""Convert genotype calls to VCF-style string representation.
Returns
-------
gt : ndarray, string, shape (n_variants, n_samples)
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[1, 2], [2, 1]],
... [[2, 2], [-1, -1]]])
>>> g.to_gt()
chararray([[b'0/0', b'0/1'],
[b'0/2', b'1/1'],
[b'1/2', b'2/1'],
[b'2/2', b'./.']],
dtype='|S3')
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(4, 2) dtype=int64>
0/0 0/2 1/2 2/2
>>> v.to_gt()
chararray([b'0/0', b'0/2', b'1/2', b'2/2'],
dtype='|S3')
>>> g.is_phased = np.ones(g.shape[:-1])
>>> g.to_gt()
chararray([[b'0|0', b'0|1'],
[b'0|2', b'1|1'],
[b'1|2', b'2|1'],
[b'2|2', b'.|.']],
dtype='|S3')
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(4, 2) dtype=int64>
0|0 0|2 1|2 2|2
>>> v.to_gt()
chararray([b'0|0', b'0|2', b'1|2', b'2|2'],
dtype='|S3')
"""
# how many characters needed per allele call?
if max_allele is None:
max_allele = np.max(self)
if max_allele <= 0:
max_allele = 1
nchar = int(np.floor(np.log10(max_allele))) + 1
# convert to string
a = self.astype((np.string_, nchar)).view(np.chararray)
# recode missing alleles
a[self < 0] = b'.'
if self.mask is not None:
a[self.mask] = b'.'
# determine allele call separator
if self.is_phased is None:
sep = b'/'
else:
sep = np.empty(self.shape[:-1], dtype='S1').view(np.chararray)
sep[self.is_phased] = b'|'
sep[~self.is_phased] = b'/'
# join via separator, coping with any ploidy
gt = a[..., 0]
for i in range(1, self.ploidy):
gt = gt + sep + a[..., i]
return gt | python | def to_gt(self, max_allele=None):
# how many characters needed per allele call?
if max_allele is None:
max_allele = np.max(self)
if max_allele <= 0:
max_allele = 1
nchar = int(np.floor(np.log10(max_allele))) + 1
# convert to string
a = self.astype((np.string_, nchar)).view(np.chararray)
# recode missing alleles
a[self < 0] = b'.'
if self.mask is not None:
a[self.mask] = b'.'
# determine allele call separator
if self.is_phased is None:
sep = b'/'
else:
sep = np.empty(self.shape[:-1], dtype='S1').view(np.chararray)
sep[self.is_phased] = b'|'
sep[~self.is_phased] = b'/'
# join via separator, coping with any ploidy
gt = a[..., 0]
for i in range(1, self.ploidy):
gt = gt + sep + a[..., i]
return gt | [
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Returns
-------
gt : ndarray, string, shape (n_variants, n_samples)
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[1, 2], [2, 1]],
... [[2, 2], [-1, -1]]])
>>> g.to_gt()
chararray([[b'0/0', b'0/1'],
[b'0/2', b'1/1'],
[b'1/2', b'2/1'],
[b'2/2', b'./.']],
dtype='|S3')
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(4, 2) dtype=int64>
0/0 0/2 1/2 2/2
>>> v.to_gt()
chararray([b'0/0', b'0/2', b'1/2', b'2/2'],
dtype='|S3')
>>> g.is_phased = np.ones(g.shape[:-1])
>>> g.to_gt()
chararray([[b'0|0', b'0|1'],
[b'0|2', b'1|1'],
[b'1|2', b'2|1'],
[b'2|2', b'.|.']],
dtype='|S3')
>>> v = g[:, 0]
>>> v
<GenotypeVector shape=(4, 2) dtype=int64>
0|0 0|2 1|2 2|2
>>> v.to_gt()
chararray([b'0|0', b'0|2', b'1|2', b'2|2'],
dtype='|S3') | [
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1,040 | cggh/scikit-allel | allel/model/ndarray.py | GenotypeArray.to_packed | def to_packed(self, boundscheck=True):
"""Pack diploid genotypes into a single byte for each genotype,
using the left-most 4 bits for the first allele and the right-most 4
bits for the second allele. Allows single byte encoding of diploid
genotypes for variants with up to 15 alleles.
Parameters
----------
boundscheck : bool, optional
If False, do not check that minimum and maximum alleles are
compatible with bit-packing.
Returns
-------
packed : ndarray, uint8, shape (n_variants, n_samples)
Bit-packed genotype array.
Notes
-----
If a mask has been set, it is ignored by this function.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[2, 2], [-1, -1]]], dtype='i1')
>>> g.to_packed()
array([[ 0, 1],
[ 2, 17],
[ 34, 239]], dtype=uint8)
"""
check_ploidy(self.ploidy, 2)
if boundscheck:
amx = self.max()
if amx > 14:
raise ValueError('max allele for packing is 14, found %s' % amx)
amn = self.min()
if amn < -1:
raise ValueError('min allele for packing is -1, found %s' % amn)
# pack data
values = memoryview_safe(self.values)
packed = genotype_array_pack_diploid(values)
return packed | python | def to_packed(self, boundscheck=True):
check_ploidy(self.ploidy, 2)
if boundscheck:
amx = self.max()
if amx > 14:
raise ValueError('max allele for packing is 14, found %s' % amx)
amn = self.min()
if amn < -1:
raise ValueError('min allele for packing is -1, found %s' % amn)
# pack data
values = memoryview_safe(self.values)
packed = genotype_array_pack_diploid(values)
return packed | [
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using the left-most 4 bits for the first allele and the right-most 4
bits for the second allele. Allows single byte encoding of diploid
genotypes for variants with up to 15 alleles.
Parameters
----------
boundscheck : bool, optional
If False, do not check that minimum and maximum alleles are
compatible with bit-packing.
Returns
-------
packed : ndarray, uint8, shape (n_variants, n_samples)
Bit-packed genotype array.
Notes
-----
If a mask has been set, it is ignored by this function.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[2, 2], [-1, -1]]], dtype='i1')
>>> g.to_packed()
array([[ 0, 1],
[ 2, 17],
[ 34, 239]], dtype=uint8) | [
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1,041 | cggh/scikit-allel | allel/model/ndarray.py | GenotypeArray.from_packed | def from_packed(cls, packed):
"""Unpack diploid genotypes that have been bit-packed into single
bytes.
Parameters
----------
packed : ndarray, uint8, shape (n_variants, n_samples)
Bit-packed diploid genotype array.
Returns
-------
g : GenotypeArray, shape (n_variants, n_samples, 2)
Genotype array.
Examples
--------
>>> import allel
>>> import numpy as np
>>> packed = np.array([[0, 1],
... [2, 17],
... [34, 239]], dtype='u1')
>>> allel.GenotypeArray.from_packed(packed)
<GenotypeArray shape=(3, 2, 2) dtype=int8>
0/0 0/1
0/2 1/1
2/2 ./.
"""
# check arguments
packed = np.asarray(packed)
check_ndim(packed, 2)
check_dtype(packed, 'u1')
packed = memoryview_safe(packed)
data = genotype_array_unpack_diploid(packed)
return cls(data) | python | def from_packed(cls, packed):
# check arguments
packed = np.asarray(packed)
check_ndim(packed, 2)
check_dtype(packed, 'u1')
packed = memoryview_safe(packed)
data = genotype_array_unpack_diploid(packed)
return cls(data) | [
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Parameters
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packed : ndarray, uint8, shape (n_variants, n_samples)
Bit-packed diploid genotype array.
Returns
-------
g : GenotypeArray, shape (n_variants, n_samples, 2)
Genotype array.
Examples
--------
>>> import allel
>>> import numpy as np
>>> packed = np.array([[0, 1],
... [2, 17],
... [34, 239]], dtype='u1')
>>> allel.GenotypeArray.from_packed(packed)
<GenotypeArray shape=(3, 2, 2) dtype=int8>
0/0 0/1
0/2 1/1
2/2 ./. | [
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1,042 | cggh/scikit-allel | allel/model/ndarray.py | GenotypeArray.from_sparse | def from_sparse(m, ploidy, order=None, out=None):
"""Construct a genotype array from a sparse matrix.
Parameters
----------
m : scipy.sparse.spmatrix
Sparse matrix
ploidy : int
The sample ploidy.
order : {'C', 'F'}, optional
Whether to store data in C (row-major) or Fortran (column-major)
order in memory.
out : ndarray, shape (n_variants, n_samples), optional
Use this array as the output buffer.
Returns
-------
g : GenotypeArray, shape (n_variants, n_samples, ploidy)
Genotype array.
Examples
--------
>>> import allel
>>> import numpy as np
>>> import scipy.sparse
>>> data = np.array([ 1, 1, 1, 1, -1, -1], dtype=np.int8)
>>> indices = np.array([1, 3, 0, 1, 2, 3], dtype=np.int32)
>>> indptr = np.array([0, 0, 2, 4, 6], dtype=np.int32)
>>> m = scipy.sparse.csr_matrix((data, indices, indptr))
>>> g = allel.GenotypeArray.from_sparse(m, ploidy=2)
>>> g
<GenotypeArray shape=(4, 2, 2) dtype=int8>
0/0 0/0
0/1 0/1
1/1 0/0
0/0 ./.
"""
h = HaplotypeArray.from_sparse(m, order=order, out=out)
g = h.to_genotypes(ploidy=ploidy)
return g | python | def from_sparse(m, ploidy, order=None, out=None):
h = HaplotypeArray.from_sparse(m, order=order, out=out)
g = h.to_genotypes(ploidy=ploidy)
return g | [
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Parameters
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m : scipy.sparse.spmatrix
Sparse matrix
ploidy : int
The sample ploidy.
order : {'C', 'F'}, optional
Whether to store data in C (row-major) or Fortran (column-major)
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out : ndarray, shape (n_variants, n_samples), optional
Use this array as the output buffer.
Returns
-------
g : GenotypeArray, shape (n_variants, n_samples, ploidy)
Genotype array.
Examples
--------
>>> import allel
>>> import numpy as np
>>> import scipy.sparse
>>> data = np.array([ 1, 1, 1, 1, -1, -1], dtype=np.int8)
>>> indices = np.array([1, 3, 0, 1, 2, 3], dtype=np.int32)
>>> indptr = np.array([0, 0, 2, 4, 6], dtype=np.int32)
>>> m = scipy.sparse.csr_matrix((data, indices, indptr))
>>> g = allel.GenotypeArray.from_sparse(m, ploidy=2)
>>> g
<GenotypeArray shape=(4, 2, 2) dtype=int8>
0/0 0/0
0/1 0/1
1/1 0/0
0/0 ./. | [
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1,043 | cggh/scikit-allel | allel/model/ndarray.py | GenotypeArray.haploidify_samples | def haploidify_samples(self):
"""Construct a pseudo-haplotype for each sample by randomly
selecting an allele from each genotype call.
Returns
-------
h : HaplotypeArray
Notes
-----
If a mask has been set, it is ignored by this function.
Examples
--------
>>> import allel
>>> import numpy as np
>>> np.random.seed(42)
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[1, 2], [2, 1]],
... [[2, 2], [-1, -1]]])
>>> g.haploidify_samples()
<HaplotypeArray shape=(4, 2) dtype=int64>
0 1
0 1
1 1
2 .
>>> g = allel.GenotypeArray([[[0, 0, 0], [0, 0, 1]],
... [[0, 1, 1], [1, 1, 1]],
... [[0, 1, 2], [-1, -1, -1]]])
>>> g.haploidify_samples()
<HaplotypeArray shape=(3, 2) dtype=int64>
0 0
1 1
2 .
"""
# N.B., this implementation is obscure and uses more memory than
# necessary, TODO review
# define the range of possible indices, e.g., diploid => (0, 1)
index_range = np.arange(0, self.ploidy, dtype='u1')
# create a random index for each genotype call
indices = np.random.choice(index_range, size=self.n_calls, replace=True)
# reshape genotype data so it's suitable for passing to np.choose
# by merging the variants and samples dimensions
choices = self.reshape(-1, self.ploidy).T
# now use random indices to haploidify
data = np.choose(indices, choices)
# reshape the haploidified data to restore the variants and samples
# dimensions
data = data.reshape((self.n_variants, self.n_samples))
# view as haplotype array
h = HaplotypeArray(data, copy=False)
return h | python | def haploidify_samples(self):
# N.B., this implementation is obscure and uses more memory than
# necessary, TODO review
# define the range of possible indices, e.g., diploid => (0, 1)
index_range = np.arange(0, self.ploidy, dtype='u1')
# create a random index for each genotype call
indices = np.random.choice(index_range, size=self.n_calls, replace=True)
# reshape genotype data so it's suitable for passing to np.choose
# by merging the variants and samples dimensions
choices = self.reshape(-1, self.ploidy).T
# now use random indices to haploidify
data = np.choose(indices, choices)
# reshape the haploidified data to restore the variants and samples
# dimensions
data = data.reshape((self.n_variants, self.n_samples))
# view as haplotype array
h = HaplotypeArray(data, copy=False)
return h | [
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Returns
-------
h : HaplotypeArray
Notes
-----
If a mask has been set, it is ignored by this function.
Examples
--------
>>> import allel
>>> import numpy as np
>>> np.random.seed(42)
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[1, 2], [2, 1]],
... [[2, 2], [-1, -1]]])
>>> g.haploidify_samples()
<HaplotypeArray shape=(4, 2) dtype=int64>
0 1
0 1
1 1
2 .
>>> g = allel.GenotypeArray([[[0, 0, 0], [0, 0, 1]],
... [[0, 1, 1], [1, 1, 1]],
... [[0, 1, 2], [-1, -1, -1]]])
>>> g.haploidify_samples()
<HaplotypeArray shape=(3, 2) dtype=int64>
0 0
1 1
2 . | [
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1,044 | cggh/scikit-allel | allel/model/ndarray.py | GenotypeArray.count_alleles_subpops | def count_alleles_subpops(self, subpops, max_allele=None):
"""Count alleles for multiple subpopulations simultaneously.
Parameters
----------
subpops : dict (string -> sequence of ints)
Mapping of subpopulation names to sample indices.
max_allele : int, optional
The highest allele index to count. Alleles above this will be
ignored.
Returns
-------
out : dict (string -> AlleleCountsArray)
A mapping of subpopulation names to allele counts arrays.
"""
if max_allele is None:
max_allele = self.max()
out = {name: self.count_alleles(max_allele=max_allele, subpop=subpop)
for name, subpop in subpops.items()}
return out | python | def count_alleles_subpops(self, subpops, max_allele=None):
if max_allele is None:
max_allele = self.max()
out = {name: self.count_alleles(max_allele=max_allele, subpop=subpop)
for name, subpop in subpops.items()}
return out | [
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Parameters
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subpops : dict (string -> sequence of ints)
Mapping of subpopulation names to sample indices.
max_allele : int, optional
The highest allele index to count. Alleles above this will be
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Returns
-------
out : dict (string -> AlleleCountsArray)
A mapping of subpopulation names to allele counts arrays. | [
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1,045 | cggh/scikit-allel | allel/model/ndarray.py | HaplotypeArray.subset | def subset(self, sel0=None, sel1=None):
"""Make a sub-selection of variants and haplotypes.
Parameters
----------
sel0 : array_like
Boolean array or array of indices selecting variants.
sel1 : array_like
Boolean array or array of indices selecting haplotypes.
Returns
-------
out : HaplotypeArray
See Also
--------
HaplotypeArray.take, HaplotypeArray.compress
"""
return subset_haplotype_array(self, sel0, sel1, cls=type(self), subset=subset) | python | def subset(self, sel0=None, sel1=None):
return subset_haplotype_array(self, sel0, sel1, cls=type(self), subset=subset) | [
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Parameters
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sel0 : array_like
Boolean array or array of indices selecting variants.
sel1 : array_like
Boolean array or array of indices selecting haplotypes.
Returns
-------
out : HaplotypeArray
See Also
--------
HaplotypeArray.take, HaplotypeArray.compress | [
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1,046 | cggh/scikit-allel | allel/model/ndarray.py | HaplotypeArray.concatenate | def concatenate(self, others, axis=0):
"""Join a sequence of arrays along an existing axis.
Parameters
----------
others : sequence of array_like
The arrays must have the same shape, except in the dimension
corresponding to `axis` (the first, by default).
axis : int, optional
The axis along which the arrays will be joined. Default is 0.
Returns
-------
res : ndarray
The concatenated array.
Examples
--------
>>> import allel
>>> h = allel.HaplotypeArray([[0, 0, 0, 1],
... [0, 1, 1, 1],
... [0, 2, -1, -1]], dtype='i1')
>>> h.concatenate([h], axis=0)
<HaplotypeArray shape=(6, 4) dtype=int8>
0 0 0 1
0 1 1 1
0 2 . .
0 0 0 1
0 1 1 1
0 2 . .
>>> h.concatenate([h], axis=1)
<HaplotypeArray shape=(3, 8) dtype=int8>
0 0 0 1 0 0 0 1
0 1 1 1 0 1 1 1
0 2 . . 0 2 . .
"""
return concatenate_haplotype_array(self, others, axis=axis, cls=type(self),
concatenate=np.concatenate) | python | def concatenate(self, others, axis=0):
return concatenate_haplotype_array(self, others, axis=axis, cls=type(self),
concatenate=np.concatenate) | [
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axis : int, optional
The axis along which the arrays will be joined. Default is 0.
Returns
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Examples
--------
>>> import allel
>>> h = allel.HaplotypeArray([[0, 0, 0, 1],
... [0, 1, 1, 1],
... [0, 2, -1, -1]], dtype='i1')
>>> h.concatenate([h], axis=0)
<HaplotypeArray shape=(6, 4) dtype=int8>
0 0 0 1
0 1 1 1
0 2 . .
0 0 0 1
0 1 1 1
0 2 . .
>>> h.concatenate([h], axis=1)
<HaplotypeArray shape=(3, 8) dtype=int8>
0 0 0 1 0 0 0 1
0 1 1 1 0 1 1 1
0 2 . . 0 2 . . | [
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1,047 | cggh/scikit-allel | allel/model/ndarray.py | HaplotypeArray.to_genotypes | def to_genotypes(self, ploidy, copy=False):
"""Reshape a haplotype array to view it as genotypes by restoring the
ploidy dimension.
Parameters
----------
ploidy : int
The sample ploidy.
copy : bool, optional
If True, make a copy of data.
Returns
-------
g : ndarray, int, shape (n_variants, n_samples, ploidy)
Genotype array (sharing same underlying buffer).
copy : bool, optional
If True, copy the data.
Examples
--------
>>> import allel
>>> h = allel.HaplotypeArray([[0, 0, 0, 1],
... [0, 1, 1, 1],
... [0, 2, -1, -1]], dtype='i1')
>>> h.to_genotypes(ploidy=2)
<GenotypeArray shape=(3, 2, 2) dtype=int8>
0/0 0/1
0/1 1/1
0/2 ./.
"""
# check ploidy is compatible
if (self.shape[1] % ploidy) > 0:
raise ValueError('incompatible ploidy')
# reshape
newshape = (self.shape[0], -1, ploidy)
data = self.reshape(newshape)
# wrap
g = GenotypeArray(data, copy=copy)
return g | python | def to_genotypes(self, ploidy, copy=False):
# check ploidy is compatible
if (self.shape[1] % ploidy) > 0:
raise ValueError('incompatible ploidy')
# reshape
newshape = (self.shape[0], -1, ploidy)
data = self.reshape(newshape)
# wrap
g = GenotypeArray(data, copy=copy)
return g | [
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ploidy dimension.
Parameters
----------
ploidy : int
The sample ploidy.
copy : bool, optional
If True, make a copy of data.
Returns
-------
g : ndarray, int, shape (n_variants, n_samples, ploidy)
Genotype array (sharing same underlying buffer).
copy : bool, optional
If True, copy the data.
Examples
--------
>>> import allel
>>> h = allel.HaplotypeArray([[0, 0, 0, 1],
... [0, 1, 1, 1],
... [0, 2, -1, -1]], dtype='i1')
>>> h.to_genotypes(ploidy=2)
<GenotypeArray shape=(3, 2, 2) dtype=int8>
0/0 0/1
0/1 1/1
0/2 ./. | [
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1,048 | cggh/scikit-allel | allel/model/ndarray.py | HaplotypeArray.from_sparse | def from_sparse(m, order=None, out=None):
"""Construct a haplotype array from a sparse matrix.
Parameters
----------
m : scipy.sparse.spmatrix
Sparse matrix
order : {'C', 'F'}, optional
Whether to store data in C (row-major) or Fortran (column-major)
order in memory.
out : ndarray, shape (n_variants, n_samples), optional
Use this array as the output buffer.
Returns
-------
h : HaplotypeArray, shape (n_variants, n_haplotypes)
Haplotype array.
Examples
--------
>>> import allel
>>> import numpy as np
>>> import scipy.sparse
>>> data = np.array([ 1, 1, 1, 1, -1, -1], dtype=np.int8)
>>> indices = np.array([1, 3, 0, 1, 2, 3], dtype=np.int32)
>>> indptr = np.array([0, 0, 2, 4, 6], dtype=np.int32)
>>> m = scipy.sparse.csr_matrix((data, indices, indptr))
>>> h = allel.HaplotypeArray.from_sparse(m)
>>> h
<HaplotypeArray shape=(4, 4) dtype=int8>
0 0 0 0
0 1 0 1
1 1 0 0
0 0 . .
"""
import scipy.sparse
# check arguments
if not scipy.sparse.isspmatrix(m):
raise ValueError('not a sparse matrix: %r' % m)
# convert to dense array
data = m.toarray(order=order, out=out)
# wrap
h = HaplotypeArray(data)
return h | python | def from_sparse(m, order=None, out=None):
import scipy.sparse
# check arguments
if not scipy.sparse.isspmatrix(m):
raise ValueError('not a sparse matrix: %r' % m)
# convert to dense array
data = m.toarray(order=order, out=out)
# wrap
h = HaplotypeArray(data)
return h | [
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Sparse matrix
order : {'C', 'F'}, optional
Whether to store data in C (row-major) or Fortran (column-major)
order in memory.
out : ndarray, shape (n_variants, n_samples), optional
Use this array as the output buffer.
Returns
-------
h : HaplotypeArray, shape (n_variants, n_haplotypes)
Haplotype array.
Examples
--------
>>> import allel
>>> import numpy as np
>>> import scipy.sparse
>>> data = np.array([ 1, 1, 1, 1, -1, -1], dtype=np.int8)
>>> indices = np.array([1, 3, 0, 1, 2, 3], dtype=np.int32)
>>> indptr = np.array([0, 0, 2, 4, 6], dtype=np.int32)
>>> m = scipy.sparse.csr_matrix((data, indices, indptr))
>>> h = allel.HaplotypeArray.from_sparse(m)
>>> h
<HaplotypeArray shape=(4, 4) dtype=int8>
0 0 0 0
0 1 0 1
1 1 0 0
0 0 . . | [
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1,049 | cggh/scikit-allel | allel/model/ndarray.py | HaplotypeArray.distinct | def distinct(self):
"""Return sets of indices for each distinct haplotype."""
# setup collection
d = collections.defaultdict(set)
# iterate over haplotypes
for i in range(self.shape[1]):
# hash the haplotype
k = hash(self.values[:, i].tobytes())
# collect
d[k].add(i)
# extract sets, sorted by most common
return sorted(d.values(), key=len, reverse=True) | python | def distinct(self):
# setup collection
d = collections.defaultdict(set)
# iterate over haplotypes
for i in range(self.shape[1]):
# hash the haplotype
k = hash(self.values[:, i].tobytes())
# collect
d[k].add(i)
# extract sets, sorted by most common
return sorted(d.values(), key=len, reverse=True) | [
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1,050 | cggh/scikit-allel | allel/model/ndarray.py | HaplotypeArray.distinct_counts | def distinct_counts(self):
"""Return counts for each distinct haplotype."""
# hash the haplotypes
k = [hash(self.values[:, i].tobytes()) for i in range(self.shape[1])]
# count and sort
# noinspection PyArgumentList
counts = sorted(collections.Counter(k).values(), reverse=True)
return np.asarray(counts) | python | def distinct_counts(self):
# hash the haplotypes
k = [hash(self.values[:, i].tobytes()) for i in range(self.shape[1])]
# count and sort
# noinspection PyArgumentList
counts = sorted(collections.Counter(k).values(), reverse=True)
return np.asarray(counts) | [
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1,051 | cggh/scikit-allel | allel/model/ndarray.py | HaplotypeArray.distinct_frequencies | def distinct_frequencies(self):
"""Return frequencies for each distinct haplotype."""
c = self.distinct_counts()
n = self.shape[1]
return c / n | python | def distinct_frequencies(self):
c = self.distinct_counts()
n = self.shape[1]
return c / n | [
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1,052 | cggh/scikit-allel | allel/model/ndarray.py | AlleleCountsArray.to_frequencies | def to_frequencies(self, fill=np.nan):
"""Compute allele frequencies.
Parameters
----------
fill : float, optional
Value to use when number of allele calls is 0.
Returns
-------
af : ndarray, float, shape (n_variants, n_alleles)
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[2, 2], [-1, -1]]])
>>> ac = g.count_alleles()
>>> ac.to_frequencies()
array([[0.75, 0.25, 0. ],
[0.25, 0.5 , 0.25],
[0. , 0. , 1. ]])
"""
an = np.sum(self, axis=1)[:, None]
with ignore_invalid():
af = np.where(an > 0, self / an, fill)
return af | python | def to_frequencies(self, fill=np.nan):
an = np.sum(self, axis=1)[:, None]
with ignore_invalid():
af = np.where(an > 0, self / an, fill)
return af | [
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Parameters
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fill : float, optional
Value to use when number of allele calls is 0.
Returns
-------
af : ndarray, float, shape (n_variants, n_alleles)
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[2, 2], [-1, -1]]])
>>> ac = g.count_alleles()
>>> ac.to_frequencies()
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1,053 | cggh/scikit-allel | allel/model/ndarray.py | AlleleCountsArray.max_allele | def max_allele(self):
"""Return the highest allele index for each variant.
Returns
-------
n : ndarray, int, shape (n_variants,)
Allele index array.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[2, 2], [-1, -1]]])
>>> ac = g.count_alleles()
>>> ac.max_allele()
array([1, 2, 2], dtype=int8)
"""
out = np.empty(self.shape[0], dtype='i1')
out.fill(-1)
for i in range(self.shape[1]):
d = self.values[:, i] > 0
out[d] = i
return out | python | def max_allele(self):
out = np.empty(self.shape[0], dtype='i1')
out.fill(-1)
for i in range(self.shape[1]):
d = self.values[:, i] > 0
out[d] = i
return out | [
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Returns
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Allele index array.
Examples
--------
>>> import allel
>>> g = allel.GenotypeArray([[[0, 0], [0, 1]],
... [[0, 2], [1, 1]],
... [[2, 2], [-1, -1]]])
>>> ac = g.count_alleles()
>>> ac.max_allele()
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1,054 | cggh/scikit-allel | allel/model/ndarray.py | SortedIndex.is_unique | def is_unique(self):
"""True if no duplicate entries."""
if self._is_unique is None:
t = self.values[:-1] == self.values[1:] # type: np.ndarray
self._is_unique = ~np.any(t)
return self._is_unique | python | def is_unique(self):
if self._is_unique is None:
t = self.values[:-1] == self.values[1:] # type: np.ndarray
self._is_unique = ~np.any(t)
return self._is_unique | [
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1,055 | cggh/scikit-allel | allel/model/ndarray.py | SortedIndex.intersect | def intersect(self, other):
"""Intersect with `other` sorted index.
Parameters
----------
other : array_like, int
Array of values to intersect with.
Returns
-------
out : SortedIndex
Values in common.
Examples
--------
>>> import allel
>>> idx1 = allel.SortedIndex([3, 6, 11, 20, 35])
>>> idx2 = allel.SortedIndex([4, 6, 20, 39])
>>> idx1.intersect(idx2)
<SortedIndex shape=(2,) dtype=int64>
[6, 20]
"""
loc = self.locate_keys(other, strict=False)
return self.compress(loc, axis=0) | python | def intersect(self, other):
loc = self.locate_keys(other, strict=False)
return self.compress(loc, axis=0) | [
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Parameters
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other : array_like, int
Array of values to intersect with.
Returns
-------
out : SortedIndex
Values in common.
Examples
--------
>>> import allel
>>> idx1 = allel.SortedIndex([3, 6, 11, 20, 35])
>>> idx2 = allel.SortedIndex([4, 6, 20, 39])
>>> idx1.intersect(idx2)
<SortedIndex shape=(2,) dtype=int64>
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1,056 | cggh/scikit-allel | allel/model/ndarray.py | SortedIndex.locate_intersection_ranges | def locate_intersection_ranges(self, starts, stops):
"""Locate the intersection with a set of ranges.
Parameters
----------
starts : array_like, int
Range start values.
stops : array_like, int
Range stop values.
Returns
-------
loc : ndarray, bool
Boolean array with location of entries found.
loc_ranges : ndarray, bool
Boolean array with location of ranges containing one or more
entries.
Examples
--------
>>> import allel
>>> import numpy as np
>>> idx = allel.SortedIndex([3, 6, 11, 20, 35])
>>> ranges = np.array([[0, 2], [6, 17], [12, 15], [31, 35],
... [100, 120]])
>>> starts = ranges[:, 0]
>>> stops = ranges[:, 1]
>>> loc, loc_ranges = idx.locate_intersection_ranges(starts, stops)
>>> loc
array([False, True, True, False, True])
>>> loc_ranges
array([False, True, False, True, False])
>>> idx[loc]
<SortedIndex shape=(3,) dtype=int64>
[6, 11, 35]
>>> ranges[loc_ranges]
array([[ 6, 17],
[31, 35]])
"""
# check inputs
starts = asarray_ndim(starts, 1)
stops = asarray_ndim(stops, 1)
check_dim0_aligned(starts, stops)
# find indices of start and stop values in idx
start_indices = np.searchsorted(self, starts)
stop_indices = np.searchsorted(self, stops, side='right')
# find intervals overlapping at least one value
loc_ranges = start_indices < stop_indices
# find values within at least one interval
loc = np.zeros(self.shape, dtype=np.bool)
for i, j in zip(start_indices[loc_ranges], stop_indices[loc_ranges]):
loc[i:j] = True
return loc, loc_ranges | python | def locate_intersection_ranges(self, starts, stops):
# check inputs
starts = asarray_ndim(starts, 1)
stops = asarray_ndim(stops, 1)
check_dim0_aligned(starts, stops)
# find indices of start and stop values in idx
start_indices = np.searchsorted(self, starts)
stop_indices = np.searchsorted(self, stops, side='right')
# find intervals overlapping at least one value
loc_ranges = start_indices < stop_indices
# find values within at least one interval
loc = np.zeros(self.shape, dtype=np.bool)
for i, j in zip(start_indices[loc_ranges], stop_indices[loc_ranges]):
loc[i:j] = True
return loc, loc_ranges | [
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Parameters
----------
starts : array_like, int
Range start values.
stops : array_like, int
Range stop values.
Returns
-------
loc : ndarray, bool
Boolean array with location of entries found.
loc_ranges : ndarray, bool
Boolean array with location of ranges containing one or more
entries.
Examples
--------
>>> import allel
>>> import numpy as np
>>> idx = allel.SortedIndex([3, 6, 11, 20, 35])
>>> ranges = np.array([[0, 2], [6, 17], [12, 15], [31, 35],
... [100, 120]])
>>> starts = ranges[:, 0]
>>> stops = ranges[:, 1]
>>> loc, loc_ranges = idx.locate_intersection_ranges(starts, stops)
>>> loc
array([False, True, True, False, True])
>>> loc_ranges
array([False, True, False, True, False])
>>> idx[loc]
<SortedIndex shape=(3,) dtype=int64>
[6, 11, 35]
>>> ranges[loc_ranges]
array([[ 6, 17],
[31, 35]]) | [
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1,057 | cggh/scikit-allel | allel/model/ndarray.py | SortedIndex.locate_ranges | def locate_ranges(self, starts, stops, strict=True):
"""Locate items within the given ranges.
Parameters
----------
starts : array_like, int
Range start values.
stops : array_like, int
Range stop values.
strict : bool, optional
If True, raise KeyError if any ranges contain no entries.
Returns
-------
loc : ndarray, bool
Boolean array with location of entries found.
Examples
--------
>>> import allel
>>> import numpy as np
>>> idx = allel.SortedIndex([3, 6, 11, 20, 35])
>>> ranges = np.array([[0, 2], [6, 17], [12, 15], [31, 35],
... [100, 120]])
>>> starts = ranges[:, 0]
>>> stops = ranges[:, 1]
>>> loc = idx.locate_ranges(starts, stops, strict=False)
>>> loc
array([False, True, True, False, True])
>>> idx[loc]
<SortedIndex shape=(3,) dtype=int64>
[6, 11, 35]
"""
loc, found = self.locate_intersection_ranges(starts, stops)
if strict and np.any(~found):
raise KeyError(starts[~found], stops[~found])
return loc | python | def locate_ranges(self, starts, stops, strict=True):
loc, found = self.locate_intersection_ranges(starts, stops)
if strict and np.any(~found):
raise KeyError(starts[~found], stops[~found])
return loc | [
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Range stop values.
strict : bool, optional
If True, raise KeyError if any ranges contain no entries.
Returns
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loc : ndarray, bool
Boolean array with location of entries found.
Examples
--------
>>> import allel
>>> import numpy as np
>>> idx = allel.SortedIndex([3, 6, 11, 20, 35])
>>> ranges = np.array([[0, 2], [6, 17], [12, 15], [31, 35],
... [100, 120]])
>>> starts = ranges[:, 0]
>>> stops = ranges[:, 1]
>>> loc = idx.locate_ranges(starts, stops, strict=False)
>>> loc
array([False, True, True, False, True])
>>> idx[loc]
<SortedIndex shape=(3,) dtype=int64>
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1,058 | cggh/scikit-allel | allel/model/ndarray.py | SortedIndex.intersect_ranges | def intersect_ranges(self, starts, stops):
"""Intersect with a set of ranges.
Parameters
----------
starts : array_like, int
Range start values.
stops : array_like, int
Range stop values.
Returns
-------
idx : SortedIndex
Examples
--------
>>> import allel
>>> import numpy as np
>>> idx = allel.SortedIndex([3, 6, 11, 20, 35])
>>> ranges = np.array([[0, 2], [6, 17], [12, 15], [31, 35],
... [100, 120]])
>>> starts = ranges[:, 0]
>>> stops = ranges[:, 1]
>>> idx.intersect_ranges(starts, stops)
<SortedIndex shape=(3,) dtype=int64>
[6, 11, 35]
"""
loc = self.locate_ranges(starts, stops, strict=False)
return self.compress(loc, axis=0) | python | def intersect_ranges(self, starts, stops):
loc = self.locate_ranges(starts, stops, strict=False)
return self.compress(loc, axis=0) | [
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Range start values.
stops : array_like, int
Range stop values.
Returns
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idx : SortedIndex
Examples
--------
>>> import allel
>>> import numpy as np
>>> idx = allel.SortedIndex([3, 6, 11, 20, 35])
>>> ranges = np.array([[0, 2], [6, 17], [12, 15], [31, 35],
... [100, 120]])
>>> starts = ranges[:, 0]
>>> stops = ranges[:, 1]
>>> idx.intersect_ranges(starts, stops)
<SortedIndex shape=(3,) dtype=int64>
[6, 11, 35] | [
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1,059 | cggh/scikit-allel | allel/model/ndarray.py | VariantTable.set_index | def set_index(self, index):
"""Set or reset the index.
Parameters
----------
index : string or pair of strings, optional
Names of columns to use for positional index, e.g., 'POS' if table
contains a 'POS' column and records from a single
chromosome/contig, or ('CHROM', 'POS') if table contains records
from multiple chromosomes/contigs.
"""
if index is None:
pass
elif isinstance(index, str):
index = SortedIndex(self[index], copy=False)
elif isinstance(index, (tuple, list)) and len(index) == 2:
index = SortedMultiIndex(self[index[0]], self[index[1]],
copy=False)
else:
raise ValueError('invalid index argument, expected string or '
'pair of strings, found %s' % repr(index))
self.index = index | python | def set_index(self, index):
if index is None:
pass
elif isinstance(index, str):
index = SortedIndex(self[index], copy=False)
elif isinstance(index, (tuple, list)) and len(index) == 2:
index = SortedMultiIndex(self[index[0]], self[index[1]],
copy=False)
else:
raise ValueError('invalid index argument, expected string or '
'pair of strings, found %s' % repr(index))
self.index = index | [
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Parameters
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index : string or pair of strings, optional
Names of columns to use for positional index, e.g., 'POS' if table
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chromosome/contig, or ('CHROM', 'POS') if table contains records
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1,060 | cggh/scikit-allel | allel/model/ndarray.py | VariantTable.query_position | def query_position(self, chrom=None, position=None):
"""Query the table, returning row or rows matching the given genomic
position.
Parameters
----------
chrom : string, optional
Chromosome/contig.
position : int, optional
Position (1-based).
Returns
-------
result : row or VariantTable
"""
if self.index is None:
raise ValueError('no index has been set')
if isinstance(self.index, SortedIndex):
# ignore chrom
loc = self.index.locate_key(position)
else:
loc = self.index.locate_key(chrom, position)
return self[loc] | python | def query_position(self, chrom=None, position=None):
if self.index is None:
raise ValueError('no index has been set')
if isinstance(self.index, SortedIndex):
# ignore chrom
loc = self.index.locate_key(position)
else:
loc = self.index.locate_key(chrom, position)
return self[loc] | [
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1,061 | cggh/scikit-allel | allel/model/ndarray.py | VariantTable.query_region | def query_region(self, chrom=None, start=None, stop=None):
"""Query the table, returning row or rows within the given genomic
region.
Parameters
----------
chrom : string, optional
Chromosome/contig.
start : int, optional
Region start position (1-based).
stop : int, optional
Region stop position (1-based).
Returns
-------
result : VariantTable
"""
if self.index is None:
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# ignore chrom
loc = self.index.locate_range(start, stop)
else:
loc = self.index.locate_range(chrom, start, stop)
return self[loc] | python | def query_region(self, chrom=None, start=None, stop=None):
if self.index is None:
raise ValueError('no index has been set')
if isinstance(self.index, SortedIndex):
# ignore chrom
loc = self.index.locate_range(start, stop)
else:
loc = self.index.locate_range(chrom, start, stop)
return self[loc] | [
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Region start position (1-based).
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Region stop position (1-based).
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1,062 | cggh/scikit-allel | allel/model/ndarray.py | FeatureTable.to_mask | def to_mask(self, size, start_name='start', stop_name='end'):
"""Construct a mask array where elements are True if the fall within
features in the table.
Parameters
----------
size : int
Size of chromosome/contig.
start_name : string, optional
Name of column with start coordinates.
stop_name : string, optional
Name of column with stop coordinates.
Returns
-------
mask : ndarray, bool
"""
m = np.zeros(size, dtype=bool)
for start, stop in self[[start_name, stop_name]]:
m[start-1:stop] = True
return m | python | def to_mask(self, size, start_name='start', stop_name='end'):
m = np.zeros(size, dtype=bool)
for start, stop in self[[start_name, stop_name]]:
m[start-1:stop] = True
return m | [
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Name of column with start coordinates.
stop_name : string, optional
Name of column with stop coordinates.
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-------
mask : ndarray, bool | [
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1,063 | cggh/scikit-allel | allel/model/ndarray.py | FeatureTable.from_gff3 | def from_gff3(path, attributes=None, region=None, score_fill=-1, phase_fill=-1,
attributes_fill='.', dtype=None):
"""Read a feature table from a GFF3 format file.
Parameters
----------
path : string
File path.
attributes : list of strings, optional
List of columns to extract from the "attributes" field.
region : string, optional
Genome region to extract. If given, file must be position
sorted, bgzipped and tabix indexed. Tabix must also be installed
and on the system path.
score_fill : int, optional
Value to use where score field has a missing value.
phase_fill : int, optional
Value to use where phase field has a missing value.
attributes_fill : object or list of objects, optional
Value(s) to use where attribute field(s) have a missing value.
dtype : numpy dtype, optional
Manually specify a dtype.
Returns
-------
ft : FeatureTable
"""
a = gff3_to_recarray(path, attributes=attributes, region=region,
score_fill=score_fill, phase_fill=phase_fill,
attributes_fill=attributes_fill, dtype=dtype)
if a is None:
return None
else:
return FeatureTable(a, copy=False) | python | def from_gff3(path, attributes=None, region=None, score_fill=-1, phase_fill=-1,
attributes_fill='.', dtype=None):
a = gff3_to_recarray(path, attributes=attributes, region=region,
score_fill=score_fill, phase_fill=phase_fill,
attributes_fill=attributes_fill, dtype=dtype)
if a is None:
return None
else:
return FeatureTable(a, copy=False) | [
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File path.
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List of columns to extract from the "attributes" field.
region : string, optional
Genome region to extract. If given, file must be position
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score_fill : int, optional
Value to use where score field has a missing value.
phase_fill : int, optional
Value to use where phase field has a missing value.
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Value(s) to use where attribute field(s) have a missing value.
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1,064 | cggh/scikit-allel | allel/stats/distance.py | pcoa | def pcoa(dist):
"""Perform principal coordinate analysis of a distance matrix, a.k.a.
classical multi-dimensional scaling.
Parameters
----------
dist : array_like
Distance matrix in condensed form.
Returns
-------
coords : ndarray, shape (n_samples, n_dimensions)
Transformed coordinates for the samples.
explained_ratio : ndarray, shape (n_dimensions)
Variance explained by each dimension.
"""
import scipy.linalg
# This implementation is based on the skbio.math.stats.ordination.PCoA
# implementation, with some minor adjustments.
# check inputs
dist = ensure_square(dist)
# perform scaling
e_matrix = (dist ** 2) / -2
row_means = np.mean(e_matrix, axis=1, keepdims=True)
col_means = np.mean(e_matrix, axis=0, keepdims=True)
matrix_mean = np.mean(e_matrix)
f_matrix = e_matrix - row_means - col_means + matrix_mean
eigvals, eigvecs = scipy.linalg.eigh(f_matrix)
# deal with eigvals close to zero
close_to_zero = np.isclose(eigvals, 0)
eigvals[close_to_zero] = 0
# sort descending
idxs = eigvals.argsort()[::-1]
eigvals = eigvals[idxs]
eigvecs = eigvecs[:, idxs]
# keep only positive eigenvalues
keep = eigvals >= 0
eigvecs = eigvecs[:, keep]
eigvals = eigvals[keep]
# compute coordinates
coords = eigvecs * np.sqrt(eigvals)
# compute ratio explained
explained_ratio = eigvals / eigvals.sum()
return coords, explained_ratio | python | def pcoa(dist):
import scipy.linalg
# This implementation is based on the skbio.math.stats.ordination.PCoA
# implementation, with some minor adjustments.
# check inputs
dist = ensure_square(dist)
# perform scaling
e_matrix = (dist ** 2) / -2
row_means = np.mean(e_matrix, axis=1, keepdims=True)
col_means = np.mean(e_matrix, axis=0, keepdims=True)
matrix_mean = np.mean(e_matrix)
f_matrix = e_matrix - row_means - col_means + matrix_mean
eigvals, eigvecs = scipy.linalg.eigh(f_matrix)
# deal with eigvals close to zero
close_to_zero = np.isclose(eigvals, 0)
eigvals[close_to_zero] = 0
# sort descending
idxs = eigvals.argsort()[::-1]
eigvals = eigvals[idxs]
eigvecs = eigvecs[:, idxs]
# keep only positive eigenvalues
keep = eigvals >= 0
eigvecs = eigvecs[:, keep]
eigvals = eigvals[keep]
# compute coordinates
coords = eigvecs * np.sqrt(eigvals)
# compute ratio explained
explained_ratio = eigvals / eigvals.sum()
return coords, explained_ratio | [
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dist : array_like
Distance matrix in condensed form.
Returns
-------
coords : ndarray, shape (n_samples, n_dimensions)
Transformed coordinates for the samples.
explained_ratio : ndarray, shape (n_dimensions)
Variance explained by each dimension. | [
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1,065 | cggh/scikit-allel | allel/stats/distance.py | condensed_coords | def condensed_coords(i, j, n):
"""Transform square distance matrix coordinates to the corresponding
index into a condensed, 1D form of the matrix.
Parameters
----------
i : int
Row index.
j : int
Column index.
n : int
Size of the square matrix (length of first or second dimension).
Returns
-------
ix : int
"""
# guard conditions
if i == j or i >= n or j >= n or i < 0 or j < 0:
raise ValueError('invalid coordinates: %s, %s' % (i, j))
# normalise order
i, j = sorted([i, j])
# calculate number of items in rows before this one (sum of arithmetic
# progression)
x = i * ((2 * n) - i - 1) / 2
# add on previous items in current row
ix = x + j - i - 1
return int(ix) | python | def condensed_coords(i, j, n):
# guard conditions
if i == j or i >= n or j >= n or i < 0 or j < 0:
raise ValueError('invalid coordinates: %s, %s' % (i, j))
# normalise order
i, j = sorted([i, j])
# calculate number of items in rows before this one (sum of arithmetic
# progression)
x = i * ((2 * n) - i - 1) / 2
# add on previous items in current row
ix = x + j - i - 1
return int(ix) | [
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1,066 | cggh/scikit-allel | allel/stats/distance.py | condensed_coords_within | def condensed_coords_within(pop, n):
"""Return indices into a condensed distance matrix for all
pairwise comparisons within the given population.
Parameters
----------
pop : array_like, int
Indices of samples or haplotypes within the population.
n : int
Size of the square matrix (length of first or second dimension).
Returns
-------
indices : ndarray, int
"""
return [condensed_coords(i, j, n)
for i, j in itertools.combinations(sorted(pop), 2)] | python | def condensed_coords_within(pop, n):
return [condensed_coords(i, j, n)
for i, j in itertools.combinations(sorted(pop), 2)] | [
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Size of the square matrix (length of first or second dimension).
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1,067 | cggh/scikit-allel | allel/stats/distance.py | condensed_coords_between | def condensed_coords_between(pop1, pop2, n):
"""Return indices into a condensed distance matrix for all pairwise
comparisons between two populations.
Parameters
----------
pop1 : array_like, int
Indices of samples or haplotypes within the first population.
pop2 : array_like, int
Indices of samples or haplotypes within the second population.
n : int
Size of the square matrix (length of first or second dimension).
Returns
-------
indices : ndarray, int
"""
return [condensed_coords(i, j, n)
for i, j in itertools.product(sorted(pop1), sorted(pop2))] | python | def condensed_coords_between(pop1, pop2, n):
return [condensed_coords(i, j, n)
for i, j in itertools.product(sorted(pop1), sorted(pop2))] | [
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1,068 | cggh/scikit-allel | allel/stats/distance.py | plot_pairwise_distance | def plot_pairwise_distance(dist, labels=None, colorbar=True, ax=None,
imshow_kwargs=None):
"""Plot a pairwise distance matrix.
Parameters
----------
dist : array_like
The distance matrix in condensed form.
labels : sequence of strings, optional
Sample labels for the axes.
colorbar : bool, optional
If True, add a colorbar to the current figure.
ax : axes, optional
The axes on which to draw. If not provided, a new figure will be
created.
imshow_kwargs : dict-like, optional
Additional keyword arguments passed through to
:func:`matplotlib.pyplot.imshow`.
Returns
-------
ax : axes
The axes on which the plot was drawn
"""
import matplotlib.pyplot as plt
# check inputs
dist_square = ensure_square(dist)
# set up axes
if ax is None:
# make a square figure
x = plt.rcParams['figure.figsize'][0]
fig, ax = plt.subplots(figsize=(x, x))
fig.tight_layout()
# setup imshow arguments
if imshow_kwargs is None:
imshow_kwargs = dict()
imshow_kwargs.setdefault('interpolation', 'none')
imshow_kwargs.setdefault('cmap', 'jet')
imshow_kwargs.setdefault('vmin', np.min(dist))
imshow_kwargs.setdefault('vmax', np.max(dist))
# plot as image
im = ax.imshow(dist_square, **imshow_kwargs)
# tidy up
if labels:
ax.set_xticks(range(len(labels)))
ax.set_yticks(range(len(labels)))
ax.set_xticklabels(labels, rotation=90)
ax.set_yticklabels(labels, rotation=0)
else:
ax.set_xticks([])
ax.set_yticks([])
if colorbar:
plt.gcf().colorbar(im, shrink=.5)
return ax | python | def plot_pairwise_distance(dist, labels=None, colorbar=True, ax=None,
imshow_kwargs=None):
import matplotlib.pyplot as plt
# check inputs
dist_square = ensure_square(dist)
# set up axes
if ax is None:
# make a square figure
x = plt.rcParams['figure.figsize'][0]
fig, ax = plt.subplots(figsize=(x, x))
fig.tight_layout()
# setup imshow arguments
if imshow_kwargs is None:
imshow_kwargs = dict()
imshow_kwargs.setdefault('interpolation', 'none')
imshow_kwargs.setdefault('cmap', 'jet')
imshow_kwargs.setdefault('vmin', np.min(dist))
imshow_kwargs.setdefault('vmax', np.max(dist))
# plot as image
im = ax.imshow(dist_square, **imshow_kwargs)
# tidy up
if labels:
ax.set_xticks(range(len(labels)))
ax.set_yticks(range(len(labels)))
ax.set_xticklabels(labels, rotation=90)
ax.set_yticklabels(labels, rotation=0)
else:
ax.set_xticks([])
ax.set_yticks([])
if colorbar:
plt.gcf().colorbar(im, shrink=.5)
return ax | [
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Parameters
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labels : sequence of strings, optional
Sample labels for the axes.
colorbar : bool, optional
If True, add a colorbar to the current figure.
ax : axes, optional
The axes on which to draw. If not provided, a new figure will be
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imshow_kwargs : dict-like, optional
Additional keyword arguments passed through to
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Returns
-------
ax : axes
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1,069 | cggh/scikit-allel | allel/stats/misc.py | jackknife | def jackknife(values, statistic):
"""Estimate standard error for `statistic` computed over `values` using
the jackknife.
Parameters
----------
values : array_like or tuple of array_like
Input array, or tuple of input arrays.
statistic : function
The statistic to compute.
Returns
-------
m : float
Mean of jackknife values.
se : float
Estimate of standard error.
vj : ndarray
Statistic values computed for each jackknife iteration.
"""
if isinstance(values, tuple):
# multiple input arrays
n = len(values[0])
masked_values = [np.ma.asarray(v) for v in values]
for m in masked_values:
assert m.ndim == 1, 'only 1D arrays supported'
assert m.shape[0] == n, 'input arrays not of equal length'
m.mask = np.zeros(m.shape, dtype=bool)
else:
n = len(values)
masked_values = np.ma.asarray(values)
assert masked_values.ndim == 1, 'only 1D arrays supported'
masked_values.mask = np.zeros(masked_values.shape, dtype=bool)
# values of the statistic calculated in each jackknife iteration
vj = list()
for i in range(n):
if isinstance(values, tuple):
# multiple input arrays
for m in masked_values:
m.mask[i] = True
x = statistic(*masked_values)
for m in masked_values:
m.mask[i] = False
else:
masked_values.mask[i] = True
x = statistic(masked_values)
masked_values.mask[i] = False
vj.append(x)
# convert to array for convenience
vj = np.array(vj)
# compute mean of jackknife values
m = vj.mean()
# compute standard error
sv = ((n - 1) / n) * np.sum((vj - m) ** 2)
se = np.sqrt(sv)
return m, se, vj | python | def jackknife(values, statistic):
if isinstance(values, tuple):
# multiple input arrays
n = len(values[0])
masked_values = [np.ma.asarray(v) for v in values]
for m in masked_values:
assert m.ndim == 1, 'only 1D arrays supported'
assert m.shape[0] == n, 'input arrays not of equal length'
m.mask = np.zeros(m.shape, dtype=bool)
else:
n = len(values)
masked_values = np.ma.asarray(values)
assert masked_values.ndim == 1, 'only 1D arrays supported'
masked_values.mask = np.zeros(masked_values.shape, dtype=bool)
# values of the statistic calculated in each jackknife iteration
vj = list()
for i in range(n):
if isinstance(values, tuple):
# multiple input arrays
for m in masked_values:
m.mask[i] = True
x = statistic(*masked_values)
for m in masked_values:
m.mask[i] = False
else:
masked_values.mask[i] = True
x = statistic(masked_values)
masked_values.mask[i] = False
vj.append(x)
# convert to array for convenience
vj = np.array(vj)
# compute mean of jackknife values
m = vj.mean()
# compute standard error
sv = ((n - 1) / n) * np.sum((vj - m) ** 2)
se = np.sqrt(sv)
return m, se, vj | [
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the jackknife.
Parameters
----------
values : array_like or tuple of array_like
Input array, or tuple of input arrays.
statistic : function
The statistic to compute.
Returns
-------
m : float
Mean of jackknife values.
se : float
Estimate of standard error.
vj : ndarray
Statistic values computed for each jackknife iteration. | [
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1,070 | cggh/scikit-allel | allel/stats/misc.py | tabulate_state_transitions | def tabulate_state_transitions(x, states, pos=None):
"""Construct a dataframe where each row provides information about a state transition.
Parameters
----------
x : array_like, int
1-dimensional array of state values.
states : set
Set of states of interest. Any state value not in this set will be ignored.
pos : array_like, int, optional
Array of positions corresponding to values in `x`.
Returns
-------
df : DataFrame
Notes
-----
The resulting dataframe includes one row at the start representing the first state
observation and one row at the end representing the last state observation.
Examples
--------
>>> import allel
>>> x = [1, 1, 0, 1, 1, 2, 2, 0, 2, 1, 1]
>>> df = allel.tabulate_state_transitions(x, states={1, 2})
>>> df
lstate rstate lidx ridx
0 -1 1 -1 0
1 1 2 4 5
2 2 1 8 9
3 1 -1 10 -1
>>> pos = [2, 4, 7, 8, 10, 14, 19, 23, 28, 30, 31]
>>> df = allel.tabulate_state_transitions(x, states={1, 2}, pos=pos)
>>> df
lstate rstate lidx ridx lpos rpos
0 -1 1 -1 0 -1 2
1 1 2 4 5 10 14
2 2 1 8 9 28 30
3 1 -1 10 -1 31 -1
"""
# check inputs
x = asarray_ndim(x, 1)
check_integer_dtype(x)
x = memoryview_safe(x)
# find state transitions
switch_points, transitions, _ = state_transitions(x, states)
# start to build a dataframe
items = [('lstate', transitions[:, 0]),
('rstate', transitions[:, 1]),
('lidx', switch_points[:, 0]),
('ridx', switch_points[:, 1])]
# deal with optional positions
if pos is not None:
pos = asarray_ndim(pos, 1)
check_dim0_aligned(x, pos)
check_integer_dtype(pos)
# find switch positions
switch_positions = np.take(pos, switch_points)
# deal with boundary transitions
switch_positions[0, 0] = -1
switch_positions[-1, 1] = -1
# add columns into dataframe
items += [('lpos', switch_positions[:, 0]),
('rpos', switch_positions[:, 1])]
import pandas
return pandas.DataFrame.from_dict(OrderedDict(items)) | python | def tabulate_state_transitions(x, states, pos=None):
# check inputs
x = asarray_ndim(x, 1)
check_integer_dtype(x)
x = memoryview_safe(x)
# find state transitions
switch_points, transitions, _ = state_transitions(x, states)
# start to build a dataframe
items = [('lstate', transitions[:, 0]),
('rstate', transitions[:, 1]),
('lidx', switch_points[:, 0]),
('ridx', switch_points[:, 1])]
# deal with optional positions
if pos is not None:
pos = asarray_ndim(pos, 1)
check_dim0_aligned(x, pos)
check_integer_dtype(pos)
# find switch positions
switch_positions = np.take(pos, switch_points)
# deal with boundary transitions
switch_positions[0, 0] = -1
switch_positions[-1, 1] = -1
# add columns into dataframe
items += [('lpos', switch_positions[:, 0]),
('rpos', switch_positions[:, 1])]
import pandas
return pandas.DataFrame.from_dict(OrderedDict(items)) | [
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Parameters
----------
x : array_like, int
1-dimensional array of state values.
states : set
Set of states of interest. Any state value not in this set will be ignored.
pos : array_like, int, optional
Array of positions corresponding to values in `x`.
Returns
-------
df : DataFrame
Notes
-----
The resulting dataframe includes one row at the start representing the first state
observation and one row at the end representing the last state observation.
Examples
--------
>>> import allel
>>> x = [1, 1, 0, 1, 1, 2, 2, 0, 2, 1, 1]
>>> df = allel.tabulate_state_transitions(x, states={1, 2})
>>> df
lstate rstate lidx ridx
0 -1 1 -1 0
1 1 2 4 5
2 2 1 8 9
3 1 -1 10 -1
>>> pos = [2, 4, 7, 8, 10, 14, 19, 23, 28, 30, 31]
>>> df = allel.tabulate_state_transitions(x, states={1, 2}, pos=pos)
>>> df
lstate rstate lidx ridx lpos rpos
0 -1 1 -1 0 -1 2
1 1 2 4 5 10 14
2 2 1 8 9 28 30
3 1 -1 10 -1 31 -1 | [
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1,071 | cggh/scikit-allel | allel/stats/misc.py | tabulate_state_blocks | def tabulate_state_blocks(x, states, pos=None):
"""Construct a dataframe where each row provides information about continuous state blocks.
Parameters
----------
x : array_like, int
1-dimensional array of state values.
states : set
Set of states of interest. Any state value not in this set will be ignored.
pos : array_like, int, optional
Array of positions corresponding to values in `x`.
Returns
-------
df : DataFrame
Examples
--------
>>> import allel
>>> x = [1, 1, 0, 1, 1, 2, 2, 0, 2, 1, 1]
>>> df = allel.tabulate_state_blocks(x, states={1, 2})
>>> df
state support start_lidx ... size_min size_max is_marginal
0 1 4 -1 ... 5 -1 True
1 2 3 4 ... 4 4 False
2 1 2 8 ... 2 -1 True
[3 rows x 9 columns]
>>> pos = [2, 4, 7, 8, 10, 14, 19, 23, 28, 30, 31]
>>> df = allel.tabulate_state_blocks(x, states={1, 2}, pos=pos)
>>> df
state support start_lidx ... stop_rpos length_min length_max
0 1 4 -1 ... 14 9 -1
1 2 3 4 ... 30 15 19
2 1 2 8 ... -1 2 -1
[3 rows x 15 columns]
"""
# check inputs
x = asarray_ndim(x, 1)
check_integer_dtype(x)
x = memoryview_safe(x)
# find state transitions
switch_points, transitions, observations = state_transitions(x, states)
# setup some helpers
t = transitions[1:, 0]
o = observations[1:]
s1 = switch_points[:-1]
s2 = switch_points[1:]
is_marginal = (s1[:, 0] < 0) | (s2[:, 1] < 0)
size_min = s2[:, 0] - s1[:, 1] + 1
size_max = s2[:, 1] - s1[:, 0] - 1
size_max[is_marginal] = -1
# start to build a dataframe
items = [
('state', t),
('support', o),
('start_lidx', s1[:, 0]),
('start_ridx', s1[:, 1]),
('stop_lidx', s2[:, 0]),
('stop_ridx', s2[:, 1]),
('size_min', size_min),
('size_max', size_max),
('is_marginal', is_marginal)
]
# deal with optional positions
if pos is not None:
pos = asarray_ndim(pos, 1)
check_dim0_aligned(x, pos)
check_integer_dtype(pos)
# obtain switch positions
switch_positions = np.take(pos, switch_points)
# deal with boundary transitions
switch_positions[0, 0] = -1
switch_positions[-1, 1] = -1
# setup helpers
p1 = switch_positions[:-1]
p2 = switch_positions[1:]
length_min = p2[:, 0] - p1[:, 1] + 1
length_max = p2[:, 1] - p1[:, 0] - 1
length_max[is_marginal] = -1
items += [
('start_lpos', p1[:, 0]),
('start_rpos', p1[:, 1]),
('stop_lpos', p2[:, 0]),
('stop_rpos', p2[:, 1]),
('length_min', length_min),
('length_max', length_max),
]
import pandas
return pandas.DataFrame.from_dict(OrderedDict(items)) | python | def tabulate_state_blocks(x, states, pos=None):
# check inputs
x = asarray_ndim(x, 1)
check_integer_dtype(x)
x = memoryview_safe(x)
# find state transitions
switch_points, transitions, observations = state_transitions(x, states)
# setup some helpers
t = transitions[1:, 0]
o = observations[1:]
s1 = switch_points[:-1]
s2 = switch_points[1:]
is_marginal = (s1[:, 0] < 0) | (s2[:, 1] < 0)
size_min = s2[:, 0] - s1[:, 1] + 1
size_max = s2[:, 1] - s1[:, 0] - 1
size_max[is_marginal] = -1
# start to build a dataframe
items = [
('state', t),
('support', o),
('start_lidx', s1[:, 0]),
('start_ridx', s1[:, 1]),
('stop_lidx', s2[:, 0]),
('stop_ridx', s2[:, 1]),
('size_min', size_min),
('size_max', size_max),
('is_marginal', is_marginal)
]
# deal with optional positions
if pos is not None:
pos = asarray_ndim(pos, 1)
check_dim0_aligned(x, pos)
check_integer_dtype(pos)
# obtain switch positions
switch_positions = np.take(pos, switch_points)
# deal with boundary transitions
switch_positions[0, 0] = -1
switch_positions[-1, 1] = -1
# setup helpers
p1 = switch_positions[:-1]
p2 = switch_positions[1:]
length_min = p2[:, 0] - p1[:, 1] + 1
length_max = p2[:, 1] - p1[:, 0] - 1
length_max[is_marginal] = -1
items += [
('start_lpos', p1[:, 0]),
('start_rpos', p1[:, 1]),
('stop_lpos', p2[:, 0]),
('stop_rpos', p2[:, 1]),
('length_min', length_min),
('length_max', length_max),
]
import pandas
return pandas.DataFrame.from_dict(OrderedDict(items)) | [
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Parameters
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x : array_like, int
1-dimensional array of state values.
states : set
Set of states of interest. Any state value not in this set will be ignored.
pos : array_like, int, optional
Array of positions corresponding to values in `x`.
Returns
-------
df : DataFrame
Examples
--------
>>> import allel
>>> x = [1, 1, 0, 1, 1, 2, 2, 0, 2, 1, 1]
>>> df = allel.tabulate_state_blocks(x, states={1, 2})
>>> df
state support start_lidx ... size_min size_max is_marginal
0 1 4 -1 ... 5 -1 True
1 2 3 4 ... 4 4 False
2 1 2 8 ... 2 -1 True
[3 rows x 9 columns]
>>> pos = [2, 4, 7, 8, 10, 14, 19, 23, 28, 30, 31]
>>> df = allel.tabulate_state_blocks(x, states={1, 2}, pos=pos)
>>> df
state support start_lidx ... stop_rpos length_min length_max
0 1 4 -1 ... 14 9 -1
1 2 3 4 ... 30 15 19
2 1 2 8 ... -1 2 -1
[3 rows x 15 columns] | [
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1,072 | cggh/scikit-allel | allel/io/vcf_write.py | write_vcf | def write_vcf(path, callset, rename=None, number=None, description=None,
fill=None, write_header=True):
"""Preliminary support for writing a VCF file. Currently does not support sample data.
Needs further work."""
names, callset = normalize_callset(callset)
with open(path, 'w') as vcf_file:
if write_header:
write_vcf_header(vcf_file, names, callset=callset, rename=rename,
number=number, description=description)
write_vcf_data(vcf_file, names, callset=callset, rename=rename, fill=fill) | python | def write_vcf(path, callset, rename=None, number=None, description=None,
fill=None, write_header=True):
names, callset = normalize_callset(callset)
with open(path, 'w') as vcf_file:
if write_header:
write_vcf_header(vcf_file, names, callset=callset, rename=rename,
number=number, description=description)
write_vcf_data(vcf_file, names, callset=callset, rename=rename, fill=fill) | [
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1,073 | cggh/scikit-allel | allel/util.py | asarray_ndim | def asarray_ndim(a, *ndims, **kwargs):
"""Ensure numpy array.
Parameters
----------
a : array_like
*ndims : int, optional
Allowed values for number of dimensions.
**kwargs
Passed through to :func:`numpy.array`.
Returns
-------
a : numpy.ndarray
"""
allow_none = kwargs.pop('allow_none', False)
kwargs.setdefault('copy', False)
if a is None and allow_none:
return None
a = np.array(a, **kwargs)
if a.ndim not in ndims:
if len(ndims) > 1:
expect_str = 'one of %s' % str(ndims)
else:
# noinspection PyUnresolvedReferences
expect_str = '%s' % ndims[0]
raise TypeError('bad number of dimensions: expected %s; found %s' %
(expect_str, a.ndim))
return a | python | def asarray_ndim(a, *ndims, **kwargs):
allow_none = kwargs.pop('allow_none', False)
kwargs.setdefault('copy', False)
if a is None and allow_none:
return None
a = np.array(a, **kwargs)
if a.ndim not in ndims:
if len(ndims) > 1:
expect_str = 'one of %s' % str(ndims)
else:
# noinspection PyUnresolvedReferences
expect_str = '%s' % ndims[0]
raise TypeError('bad number of dimensions: expected %s; found %s' %
(expect_str, a.ndim))
return a | [
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Parameters
----------
a : array_like
*ndims : int, optional
Allowed values for number of dimensions.
**kwargs
Passed through to :func:`numpy.array`.
Returns
-------
a : numpy.ndarray | [
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1,074 | cggh/scikit-allel | allel/util.py | hdf5_cache | def hdf5_cache(filepath=None, parent=None, group=None, names=None, typed=False,
hashed_key=False, **h5dcreate_kwargs):
"""HDF5 cache decorator.
Parameters
----------
filepath : string, optional
Path to HDF5 file. If None a temporary file name will be used.
parent : string, optional
Path to group within HDF5 file to use as parent. If None the root
group will be used.
group : string, optional
Path to group within HDF5 file, relative to parent, to use as
container for cached data. If None the name of the wrapped function
will be used.
names : sequence of strings, optional
Name(s) of dataset(s). If None, default names will be 'f00', 'f01',
etc.
typed : bool, optional
If True, arguments of different types will be cached separately.
For example, f(3.0) and f(3) will be treated as distinct calls with
distinct results.
hashed_key : bool, optional
If False (default) the key will not be hashed, which makes for
readable cache group names. If True the key will be hashed, however
note that on Python >= 3.3 the hash value will not be the same between
sessions unless the environment variable PYTHONHASHSEED has been set
to the same value.
Returns
-------
decorator : function
Examples
--------
Without any arguments, will cache using a temporary HDF5 file::
>>> import allel
>>> @allel.util.hdf5_cache()
... def foo(n):
... print('executing foo')
... return np.arange(n)
...
>>> foo(3)
executing foo
array([0, 1, 2])
>>> foo(3)
array([0, 1, 2])
>>> foo.cache_filepath # doctest: +SKIP
'/tmp/tmp_jwtwgjz'
Supports multiple return values, including scalars, e.g.::
>>> @allel.util.hdf5_cache()
... def bar(n):
... print('executing bar')
... a = np.arange(n)
... return a, a**2, n**2
...
>>> bar(3)
executing bar
(array([0, 1, 2]), array([0, 1, 4]), 9)
>>> bar(3)
(array([0, 1, 2]), array([0, 1, 4]), 9)
Names can also be specified for the datasets, e.g.::
>>> @allel.util.hdf5_cache(names=['z', 'x', 'y'])
... def baz(n):
... print('executing baz')
... a = np.arange(n)
... return a, a**2, n**2
...
>>> baz(3)
executing baz
(array([0, 1, 2]), array([0, 1, 4]), 9)
>>> baz(3)
(array([0, 1, 2]), array([0, 1, 4]), 9)
"""
# initialise HDF5 file path
if filepath is None:
import tempfile
filepath = tempfile.mktemp(prefix='scikit_allel_', suffix='.h5')
atexit.register(os.remove, filepath)
# initialise defaults for dataset creation
h5dcreate_kwargs.setdefault('chunks', True)
def decorator(user_function):
# setup the name for the cache container group
if group is None:
container = user_function.__name__
else:
container = group
def wrapper(*args, **kwargs):
# load from cache or not
no_cache = kwargs.pop('no_cache', False)
# compute a key from the function arguments
key = _make_key(args, kwargs, typed)
if hashed_key:
key = str(hash(key))
else:
key = str(key).replace('/', '__slash__')
return _hdf5_cache_act(filepath, parent, container, key, names,
no_cache, user_function, args, kwargs,
h5dcreate_kwargs)
wrapper.cache_filepath = filepath
return update_wrapper(wrapper, user_function)
return decorator | python | def hdf5_cache(filepath=None, parent=None, group=None, names=None, typed=False,
hashed_key=False, **h5dcreate_kwargs):
# initialise HDF5 file path
if filepath is None:
import tempfile
filepath = tempfile.mktemp(prefix='scikit_allel_', suffix='.h5')
atexit.register(os.remove, filepath)
# initialise defaults for dataset creation
h5dcreate_kwargs.setdefault('chunks', True)
def decorator(user_function):
# setup the name for the cache container group
if group is None:
container = user_function.__name__
else:
container = group
def wrapper(*args, **kwargs):
# load from cache or not
no_cache = kwargs.pop('no_cache', False)
# compute a key from the function arguments
key = _make_key(args, kwargs, typed)
if hashed_key:
key = str(hash(key))
else:
key = str(key).replace('/', '__slash__')
return _hdf5_cache_act(filepath, parent, container, key, names,
no_cache, user_function, args, kwargs,
h5dcreate_kwargs)
wrapper.cache_filepath = filepath
return update_wrapper(wrapper, user_function)
return decorator | [
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Parameters
----------
filepath : string, optional
Path to HDF5 file. If None a temporary file name will be used.
parent : string, optional
Path to group within HDF5 file to use as parent. If None the root
group will be used.
group : string, optional
Path to group within HDF5 file, relative to parent, to use as
container for cached data. If None the name of the wrapped function
will be used.
names : sequence of strings, optional
Name(s) of dataset(s). If None, default names will be 'f00', 'f01',
etc.
typed : bool, optional
If True, arguments of different types will be cached separately.
For example, f(3.0) and f(3) will be treated as distinct calls with
distinct results.
hashed_key : bool, optional
If False (default) the key will not be hashed, which makes for
readable cache group names. If True the key will be hashed, however
note that on Python >= 3.3 the hash value will not be the same between
sessions unless the environment variable PYTHONHASHSEED has been set
to the same value.
Returns
-------
decorator : function
Examples
--------
Without any arguments, will cache using a temporary HDF5 file::
>>> import allel
>>> @allel.util.hdf5_cache()
... def foo(n):
... print('executing foo')
... return np.arange(n)
...
>>> foo(3)
executing foo
array([0, 1, 2])
>>> foo(3)
array([0, 1, 2])
>>> foo.cache_filepath # doctest: +SKIP
'/tmp/tmp_jwtwgjz'
Supports multiple return values, including scalars, e.g.::
>>> @allel.util.hdf5_cache()
... def bar(n):
... print('executing bar')
... a = np.arange(n)
... return a, a**2, n**2
...
>>> bar(3)
executing bar
(array([0, 1, 2]), array([0, 1, 4]), 9)
>>> bar(3)
(array([0, 1, 2]), array([0, 1, 4]), 9)
Names can also be specified for the datasets, e.g.::
>>> @allel.util.hdf5_cache(names=['z', 'x', 'y'])
... def baz(n):
... print('executing baz')
... a = np.arange(n)
... return a, a**2, n**2
...
>>> baz(3)
executing baz
(array([0, 1, 2]), array([0, 1, 4]), 9)
>>> baz(3)
(array([0, 1, 2]), array([0, 1, 4]), 9) | [
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] | 3c979a57a100240ba959dd13f98839349530f215 | https://github.com/cggh/scikit-allel/blob/3c979a57a100240ba959dd13f98839349530f215/allel/util.py#L283-L401 |
1,075 | cggh/scikit-allel | allel/stats/decomposition.py | pca | def pca(gn, n_components=10, copy=True, scaler='patterson', ploidy=2):
"""Perform principal components analysis of genotype data, via singular
value decomposition.
Parameters
----------
gn : array_like, float, shape (n_variants, n_samples)
Genotypes at biallelic variants, coded as the number of alternate
alleles per call (i.e., 0 = hom ref, 1 = het, 2 = hom alt).
n_components : int, optional
Number of components to keep.
copy : bool, optional
If False, data passed to fit are overwritten.
scaler : {'patterson', 'standard', None}
Scaling method; 'patterson' applies the method of Patterson et al
2006; 'standard' scales to unit variance; None centers the data only.
ploidy : int, optional
Sample ploidy, only relevant if 'patterson' scaler is used.
Returns
-------
coords : ndarray, float, shape (n_samples, n_components)
Transformed coordinates for the samples.
model : GenotypePCA
Model instance containing the variance ratio explained and the stored
components (a.k.a., loadings). Can be used to project further data
into the same principal components space via the transform() method.
Notes
-----
Genotype data should be filtered prior to using this function to remove
variants in linkage disequilibrium.
See Also
--------
randomized_pca, allel.stats.ld.locate_unlinked
"""
# set up the model
model = GenotypePCA(n_components, copy=copy, scaler=scaler, ploidy=ploidy)
# fit the model and project the input data onto the new dimensions
coords = model.fit_transform(gn)
return coords, model | python | def pca(gn, n_components=10, copy=True, scaler='patterson', ploidy=2):
# set up the model
model = GenotypePCA(n_components, copy=copy, scaler=scaler, ploidy=ploidy)
# fit the model and project the input data onto the new dimensions
coords = model.fit_transform(gn)
return coords, model | [
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gn : array_like, float, shape (n_variants, n_samples)
Genotypes at biallelic variants, coded as the number of alternate
alleles per call (i.e., 0 = hom ref, 1 = het, 2 = hom alt).
n_components : int, optional
Number of components to keep.
copy : bool, optional
If False, data passed to fit are overwritten.
scaler : {'patterson', 'standard', None}
Scaling method; 'patterson' applies the method of Patterson et al
2006; 'standard' scales to unit variance; None centers the data only.
ploidy : int, optional
Sample ploidy, only relevant if 'patterson' scaler is used.
Returns
-------
coords : ndarray, float, shape (n_samples, n_components)
Transformed coordinates for the samples.
model : GenotypePCA
Model instance containing the variance ratio explained and the stored
components (a.k.a., loadings). Can be used to project further data
into the same principal components space via the transform() method.
Notes
-----
Genotype data should be filtered prior to using this function to remove
variants in linkage disequilibrium.
See Also
--------
randomized_pca, allel.stats.ld.locate_unlinked | [
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1,076 | cggh/scikit-allel | allel/stats/decomposition.py | randomized_pca | def randomized_pca(gn, n_components=10, copy=True, iterated_power=3,
random_state=None, scaler='patterson', ploidy=2):
"""Perform principal components analysis of genotype data, via an
approximate truncated singular value decomposition using randomization
to speed up the computation.
Parameters
----------
gn : array_like, float, shape (n_variants, n_samples)
Genotypes at biallelic variants, coded as the number of alternate
alleles per call (i.e., 0 = hom ref, 1 = het, 2 = hom alt).
n_components : int, optional
Number of components to keep.
copy : bool, optional
If False, data passed to fit are overwritten.
iterated_power : int, optional
Number of iterations for the power method.
random_state : int or RandomState instance or None (default)
Pseudo Random Number generator seed control. If None, use the
numpy.random singleton.
scaler : {'patterson', 'standard', None}
Scaling method; 'patterson' applies the method of Patterson et al
2006; 'standard' scales to unit variance; None centers the data only.
ploidy : int, optional
Sample ploidy, only relevant if 'patterson' scaler is used.
Returns
-------
coords : ndarray, float, shape (n_samples, n_components)
Transformed coordinates for the samples.
model : GenotypeRandomizedPCA
Model instance containing the variance ratio explained and the stored
components (a.k.a., loadings). Can be used to project further data
into the same principal components space via the transform() method.
Notes
-----
Genotype data should be filtered prior to using this function to remove
variants in linkage disequilibrium.
Based on the :class:`sklearn.decomposition.RandomizedPCA` implementation.
See Also
--------
pca, allel.stats.ld.locate_unlinked
"""
# set up the model
model = GenotypeRandomizedPCA(n_components, copy=copy,
iterated_power=iterated_power,
random_state=random_state, scaler=scaler,
ploidy=ploidy)
# fit the model and project the input data onto the new dimensions
coords = model.fit_transform(gn)
return coords, model | python | def randomized_pca(gn, n_components=10, copy=True, iterated_power=3,
random_state=None, scaler='patterson', ploidy=2):
# set up the model
model = GenotypeRandomizedPCA(n_components, copy=copy,
iterated_power=iterated_power,
random_state=random_state, scaler=scaler,
ploidy=ploidy)
# fit the model and project the input data onto the new dimensions
coords = model.fit_transform(gn)
return coords, model | [
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gn : array_like, float, shape (n_variants, n_samples)
Genotypes at biallelic variants, coded as the number of alternate
alleles per call (i.e., 0 = hom ref, 1 = het, 2 = hom alt).
n_components : int, optional
Number of components to keep.
copy : bool, optional
If False, data passed to fit are overwritten.
iterated_power : int, optional
Number of iterations for the power method.
random_state : int or RandomState instance or None (default)
Pseudo Random Number generator seed control. If None, use the
numpy.random singleton.
scaler : {'patterson', 'standard', None}
Scaling method; 'patterson' applies the method of Patterson et al
2006; 'standard' scales to unit variance; None centers the data only.
ploidy : int, optional
Sample ploidy, only relevant if 'patterson' scaler is used.
Returns
-------
coords : ndarray, float, shape (n_samples, n_components)
Transformed coordinates for the samples.
model : GenotypeRandomizedPCA
Model instance containing the variance ratio explained and the stored
components (a.k.a., loadings). Can be used to project further data
into the same principal components space via the transform() method.
Notes
-----
Genotype data should be filtered prior to using this function to remove
variants in linkage disequilibrium.
Based on the :class:`sklearn.decomposition.RandomizedPCA` implementation.
See Also
--------
pca, allel.stats.ld.locate_unlinked | [
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1,077 | cggh/scikit-allel | allel/model/dask.py | get_chunks | def get_chunks(data, chunks=None):
"""Try to guess a reasonable chunk shape to use for block-wise
algorithms operating over `data`."""
if chunks is None:
if hasattr(data, 'chunklen') and hasattr(data, 'shape'):
# bcolz carray, chunk first dimension only
return (data.chunklen,) + data.shape[1:]
elif hasattr(data, 'chunks') and hasattr(data, 'shape') and \
len(data.chunks) == len(data.shape):
# h5py dataset or zarr array
return data.chunks
else:
# fall back to something simple, ~4Mb chunks of first dimension
row = np.asarray(data[0])
chunklen = max(1, (2**22) // row.nbytes)
if row.shape:
chunks = (chunklen,) + row.shape
else:
chunks = (chunklen,)
return chunks
else:
return chunks | python | def get_chunks(data, chunks=None):
if chunks is None:
if hasattr(data, 'chunklen') and hasattr(data, 'shape'):
# bcolz carray, chunk first dimension only
return (data.chunklen,) + data.shape[1:]
elif hasattr(data, 'chunks') and hasattr(data, 'shape') and \
len(data.chunks) == len(data.shape):
# h5py dataset or zarr array
return data.chunks
else:
# fall back to something simple, ~4Mb chunks of first dimension
row = np.asarray(data[0])
chunklen = max(1, (2**22) // row.nbytes)
if row.shape:
chunks = (chunklen,) + row.shape
else:
chunks = (chunklen,)
return chunks
else:
return chunks | [
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1,078 | cggh/scikit-allel | allel/io/gff.py | iter_gff3 | def iter_gff3(path, attributes=None, region=None, score_fill=-1,
phase_fill=-1, attributes_fill='.', tabix='tabix'):
"""Iterate over records in a GFF3 file.
Parameters
----------
path : string
Path to input file.
attributes : list of strings, optional
List of columns to extract from the "attributes" field.
region : string, optional
Genome region to extract. If given, file must be position
sorted, bgzipped and tabix indexed. Tabix must also be installed
and on the system path.
score_fill : int, optional
Value to use where score field has a missing value.
phase_fill : int, optional
Value to use where phase field has a missing value.
attributes_fill : object or list of objects, optional
Value(s) to use where attribute field(s) have a missing value.
tabix : string
Tabix command.
Returns
-------
Iterator
"""
# prepare fill values for attributes
if attributes is not None:
attributes = list(attributes)
if isinstance(attributes_fill, (list, tuple)):
if len(attributes) != len(attributes_fill):
raise ValueError('number of fills does not match attributes')
else:
attributes_fill = [attributes_fill] * len(attributes)
# open input stream
if region is not None:
cmd = [tabix, path, region]
buffer = subprocess.Popen(cmd, stdout=subprocess.PIPE).stdout
elif path.endswith('.gz') or path.endswith('.bgz'):
buffer = gzip.open(path, mode='rb')
else:
buffer = open(path, mode='rb')
try:
for line in buffer:
if line[0] == b'>':
# assume begin embedded FASTA
return
if line[0] == b'#':
# skip comment lines
continue
vals = line.split(b'\t')
if len(vals) == 9:
# unpack for processing
fseqid, fsource, ftype, fstart, fend, fscore, fstrand, fphase, fattrs = vals
# convert numerics
fstart = int(fstart)
fend = int(fend)
if fscore == b'.':
fscore = score_fill
else:
fscore = float(fscore)
if fphase == b'.':
fphase = phase_fill
else:
fphase = int(fphase)
if not PY2:
fseqid = str(fseqid, 'ascii')
fsource = str(fsource, 'ascii')
ftype = str(ftype, 'ascii')
fstrand = str(fstrand, 'ascii')
fattrs = str(fattrs, 'ascii')
rec = (fseqid, fsource, ftype, fstart, fend, fscore, fstrand, fphase)
if attributes is not None:
dattrs = gff3_parse_attributes(fattrs)
vattrs = tuple(
dattrs.get(k, f)
for k, f in zip(attributes, attributes_fill)
)
rec += vattrs
yield rec
finally:
buffer.close() | python | def iter_gff3(path, attributes=None, region=None, score_fill=-1,
phase_fill=-1, attributes_fill='.', tabix='tabix'):
# prepare fill values for attributes
if attributes is not None:
attributes = list(attributes)
if isinstance(attributes_fill, (list, tuple)):
if len(attributes) != len(attributes_fill):
raise ValueError('number of fills does not match attributes')
else:
attributes_fill = [attributes_fill] * len(attributes)
# open input stream
if region is not None:
cmd = [tabix, path, region]
buffer = subprocess.Popen(cmd, stdout=subprocess.PIPE).stdout
elif path.endswith('.gz') or path.endswith('.bgz'):
buffer = gzip.open(path, mode='rb')
else:
buffer = open(path, mode='rb')
try:
for line in buffer:
if line[0] == b'>':
# assume begin embedded FASTA
return
if line[0] == b'#':
# skip comment lines
continue
vals = line.split(b'\t')
if len(vals) == 9:
# unpack for processing
fseqid, fsource, ftype, fstart, fend, fscore, fstrand, fphase, fattrs = vals
# convert numerics
fstart = int(fstart)
fend = int(fend)
if fscore == b'.':
fscore = score_fill
else:
fscore = float(fscore)
if fphase == b'.':
fphase = phase_fill
else:
fphase = int(fphase)
if not PY2:
fseqid = str(fseqid, 'ascii')
fsource = str(fsource, 'ascii')
ftype = str(ftype, 'ascii')
fstrand = str(fstrand, 'ascii')
fattrs = str(fattrs, 'ascii')
rec = (fseqid, fsource, ftype, fstart, fend, fscore, fstrand, fphase)
if attributes is not None:
dattrs = gff3_parse_attributes(fattrs)
vattrs = tuple(
dattrs.get(k, f)
for k, f in zip(attributes, attributes_fill)
)
rec += vattrs
yield rec
finally:
buffer.close() | [
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Parameters
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path : string
Path to input file.
attributes : list of strings, optional
List of columns to extract from the "attributes" field.
region : string, optional
Genome region to extract. If given, file must be position
sorted, bgzipped and tabix indexed. Tabix must also be installed
and on the system path.
score_fill : int, optional
Value to use where score field has a missing value.
phase_fill : int, optional
Value to use where phase field has a missing value.
attributes_fill : object or list of objects, optional
Value(s) to use where attribute field(s) have a missing value.
tabix : string
Tabix command.
Returns
-------
Iterator | [
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] | 3c979a57a100240ba959dd13f98839349530f215 | https://github.com/cggh/scikit-allel/blob/3c979a57a100240ba959dd13f98839349530f215/allel/io/gff.py#L31-L118 |
1,079 | cggh/scikit-allel | allel/io/gff.py | gff3_to_recarray | def gff3_to_recarray(path, attributes=None, region=None, score_fill=-1,
phase_fill=-1, attributes_fill='.', tabix='tabix', dtype=None):
"""Load data from a GFF3 into a NumPy recarray.
Parameters
----------
path : string
Path to input file.
attributes : list of strings, optional
List of columns to extract from the "attributes" field.
region : string, optional
Genome region to extract. If given, file must be position
sorted, bgzipped and tabix indexed. Tabix must also be installed
and on the system path.
score_fill : int, optional
Value to use where score field has a missing value.
phase_fill : int, optional
Value to use where phase field has a missing value.
attributes_fill : object or list of objects, optional
Value(s) to use where attribute field(s) have a missing value.
tabix : string, optional
Tabix command.
dtype : dtype, optional
Override dtype.
Returns
-------
np.recarray
"""
# read records
recs = list(iter_gff3(path, attributes=attributes, region=region,
score_fill=score_fill, phase_fill=phase_fill,
attributes_fill=attributes_fill, tabix=tabix))
if not recs:
return None
# determine dtype
if dtype is None:
dtype = [('seqid', object),
('source', object),
('type', object),
('start', int),
('end', int),
('score', float),
('strand', object),
('phase', int)]
if attributes:
for n in attributes:
dtype.append((n, object))
a = np.rec.fromrecords(recs, dtype=dtype)
return a | python | def gff3_to_recarray(path, attributes=None, region=None, score_fill=-1,
phase_fill=-1, attributes_fill='.', tabix='tabix', dtype=None):
# read records
recs = list(iter_gff3(path, attributes=attributes, region=region,
score_fill=score_fill, phase_fill=phase_fill,
attributes_fill=attributes_fill, tabix=tabix))
if not recs:
return None
# determine dtype
if dtype is None:
dtype = [('seqid', object),
('source', object),
('type', object),
('start', int),
('end', int),
('score', float),
('strand', object),
('phase', int)]
if attributes:
for n in attributes:
dtype.append((n, object))
a = np.rec.fromrecords(recs, dtype=dtype)
return a | [
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Parameters
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path : string
Path to input file.
attributes : list of strings, optional
List of columns to extract from the "attributes" field.
region : string, optional
Genome region to extract. If given, file must be position
sorted, bgzipped and tabix indexed. Tabix must also be installed
and on the system path.
score_fill : int, optional
Value to use where score field has a missing value.
phase_fill : int, optional
Value to use where phase field has a missing value.
attributes_fill : object or list of objects, optional
Value(s) to use where attribute field(s) have a missing value.
tabix : string, optional
Tabix command.
dtype : dtype, optional
Override dtype.
Returns
-------
np.recarray | [
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1,080 | cggh/scikit-allel | allel/io/gff.py | gff3_to_dataframe | def gff3_to_dataframe(path, attributes=None, region=None, score_fill=-1,
phase_fill=-1, attributes_fill='.', tabix='tabix', **kwargs):
"""Load data from a GFF3 into a pandas DataFrame.
Parameters
----------
path : string
Path to input file.
attributes : list of strings, optional
List of columns to extract from the "attributes" field.
region : string, optional
Genome region to extract. If given, file must be position
sorted, bgzipped and tabix indexed. Tabix must also be installed
and on the system path.
score_fill : int, optional
Value to use where score field has a missing value.
phase_fill : int, optional
Value to use where phase field has a missing value.
attributes_fill : object or list of objects, optional
Value(s) to use where attribute field(s) have a missing value.
tabix : string, optional
Tabix command.
Returns
-------
pandas.DataFrame
"""
import pandas
# read records
recs = list(iter_gff3(path, attributes=attributes, region=region,
score_fill=score_fill, phase_fill=phase_fill,
attributes_fill=attributes_fill, tabix=tabix))
# load into pandas
columns = ['seqid', 'source', 'type', 'start', 'end', 'score', 'strand', 'phase']
if attributes:
columns += list(attributes)
df = pandas.DataFrame.from_records(recs, columns=columns, **kwargs)
return df | python | def gff3_to_dataframe(path, attributes=None, region=None, score_fill=-1,
phase_fill=-1, attributes_fill='.', tabix='tabix', **kwargs):
import pandas
# read records
recs = list(iter_gff3(path, attributes=attributes, region=region,
score_fill=score_fill, phase_fill=phase_fill,
attributes_fill=attributes_fill, tabix=tabix))
# load into pandas
columns = ['seqid', 'source', 'type', 'start', 'end', 'score', 'strand', 'phase']
if attributes:
columns += list(attributes)
df = pandas.DataFrame.from_records(recs, columns=columns, **kwargs)
return df | [
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Parameters
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path : string
Path to input file.
attributes : list of strings, optional
List of columns to extract from the "attributes" field.
region : string, optional
Genome region to extract. If given, file must be position
sorted, bgzipped and tabix indexed. Tabix must also be installed
and on the system path.
score_fill : int, optional
Value to use where score field has a missing value.
phase_fill : int, optional
Value to use where phase field has a missing value.
attributes_fill : object or list of objects, optional
Value(s) to use where attribute field(s) have a missing value.
tabix : string, optional
Tabix command.
Returns
-------
pandas.DataFrame | [
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1,081 | cggh/scikit-allel | allel/stats/selection.py | voight_painting | def voight_painting(h):
"""Paint haplotypes, assigning a unique integer to each shared haplotype
prefix.
Parameters
----------
h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
Returns
-------
painting : ndarray, int, shape (n_variants, n_haplotypes)
Painting array.
indices : ndarray, int, shape (n_hapotypes,)
Haplotype indices after sorting by prefix.
"""
# check inputs
# N.B., ensure int8 so we can use cython optimisation
h = HaplotypeArray(np.asarray(h), copy=False)
if h.max() > 1:
raise NotImplementedError('only biallelic variants are supported')
if h.min() < 0:
raise NotImplementedError('missing calls are not supported')
# sort by prefix
indices = h.prefix_argsort()
h = np.take(h, indices, axis=1)
# paint
painting = paint_shared_prefixes(memoryview_safe(np.asarray(h)))
return painting, indices | python | def voight_painting(h):
# check inputs
# N.B., ensure int8 so we can use cython optimisation
h = HaplotypeArray(np.asarray(h), copy=False)
if h.max() > 1:
raise NotImplementedError('only biallelic variants are supported')
if h.min() < 0:
raise NotImplementedError('missing calls are not supported')
# sort by prefix
indices = h.prefix_argsort()
h = np.take(h, indices, axis=1)
# paint
painting = paint_shared_prefixes(memoryview_safe(np.asarray(h)))
return painting, indices | [
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prefix.
Parameters
----------
h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
Returns
-------
painting : ndarray, int, shape (n_variants, n_haplotypes)
Painting array.
indices : ndarray, int, shape (n_hapotypes,)
Haplotype indices after sorting by prefix. | [
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1,082 | cggh/scikit-allel | allel/stats/selection.py | plot_voight_painting | def plot_voight_painting(painting, palette='colorblind', flank='right',
ax=None, height_factor=0.01):
"""Plot a painting of shared haplotype prefixes.
Parameters
----------
painting : array_like, int, shape (n_variants, n_haplotypes)
Painting array.
ax : axes, optional
The axes on which to draw. If not provided, a new figure will be
created.
palette : string, optional
A Seaborn palette name.
flank : {'right', 'left'}, optional
If left, painting will be reversed along first axis.
height_factor : float, optional
If no axes provided, determine height of figure by multiplying
height of painting array by this number.
Returns
-------
ax : axes
"""
import seaborn as sns
from matplotlib.colors import ListedColormap
import matplotlib.pyplot as plt
if flank == 'left':
painting = painting[::-1]
n_colors = painting.max()
palette = sns.color_palette(palette, n_colors)
# use white for singleton haplotypes
cmap = ListedColormap(['white'] + palette)
# setup axes
if ax is None:
w = plt.rcParams['figure.figsize'][0]
h = height_factor*painting.shape[1]
fig, ax = plt.subplots(figsize=(w, h))
sns.despine(ax=ax, bottom=True, left=True)
ax.pcolormesh(painting.T, cmap=cmap)
ax.set_xticks([])
ax.set_yticks([])
ax.set_xlim(0, painting.shape[0])
ax.set_ylim(0, painting.shape[1])
return ax | python | def plot_voight_painting(painting, palette='colorblind', flank='right',
ax=None, height_factor=0.01):
import seaborn as sns
from matplotlib.colors import ListedColormap
import matplotlib.pyplot as plt
if flank == 'left':
painting = painting[::-1]
n_colors = painting.max()
palette = sns.color_palette(palette, n_colors)
# use white for singleton haplotypes
cmap = ListedColormap(['white'] + palette)
# setup axes
if ax is None:
w = plt.rcParams['figure.figsize'][0]
h = height_factor*painting.shape[1]
fig, ax = plt.subplots(figsize=(w, h))
sns.despine(ax=ax, bottom=True, left=True)
ax.pcolormesh(painting.T, cmap=cmap)
ax.set_xticks([])
ax.set_yticks([])
ax.set_xlim(0, painting.shape[0])
ax.set_ylim(0, painting.shape[1])
return ax | [
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Parameters
----------
painting : array_like, int, shape (n_variants, n_haplotypes)
Painting array.
ax : axes, optional
The axes on which to draw. If not provided, a new figure will be
created.
palette : string, optional
A Seaborn palette name.
flank : {'right', 'left'}, optional
If left, painting will be reversed along first axis.
height_factor : float, optional
If no axes provided, determine height of figure by multiplying
height of painting array by this number.
Returns
-------
ax : axes | [
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] | 3c979a57a100240ba959dd13f98839349530f215 | https://github.com/cggh/scikit-allel/blob/3c979a57a100240ba959dd13f98839349530f215/allel/stats/selection.py#L98-L148 |
1,083 | cggh/scikit-allel | allel/stats/selection.py | fig_voight_painting | def fig_voight_painting(h, index=None, palette='colorblind',
height_factor=0.01, fig=None):
"""Make a figure of shared haplotype prefixes for both left and right
flanks, centred on some variant of choice.
Parameters
----------
h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
index : int, optional
Index of the variant within the haplotype array to centre on. If not
provided, the middle variant will be used.
palette : string, optional
A Seaborn palette name.
height_factor : float, optional
If no axes provided, determine height of figure by multiplying
height of painting array by this number.
fig : figure
The figure on which to draw. If not provided, a new figure will be
created.
Returns
-------
fig : figure
Notes
-----
N.B., the ordering of haplotypes on the left and right flanks will be
different. This means that haplotypes on the right flank **will not**
correspond to haplotypes on the left flank at the same vertical position.
"""
import matplotlib.pyplot as plt
from matplotlib.gridspec import GridSpec
import seaborn as sns
# check inputs
h = asarray_ndim(h, 2)
if index is None:
# use midpoint
index = h.shape[0] // 2
# divide data into two flanks
hl = h[:index+1][::-1]
hr = h[index:]
# paint both flanks
pl, il = voight_painting(hl)
pr, ir = voight_painting(hr)
# compute ehh decay for both flanks
el = ehh_decay(hl, truncate=False)
er = ehh_decay(hr, truncate=False)
# setup figure
# fixed height for EHH decay subplot
h_ehh = plt.rcParams['figure.figsize'][1] // 3
# add height for paintings
h_painting = height_factor*h.shape[1]
if fig is None:
w = plt.rcParams['figure.figsize'][0]
h = h_ehh + h_painting
fig = plt.figure(figsize=(w, h))
# setup gridspec
gs = GridSpec(2, 2,
width_ratios=[hl.shape[0], hr.shape[0]],
height_ratios=[h_painting, h_ehh])
# plot paintings
ax = fig.add_subplot(gs[0, 0])
sns.despine(ax=ax, left=True, bottom=True)
plot_voight_painting(pl, palette=palette, flank='left', ax=ax)
ax = fig.add_subplot(gs[0, 1])
sns.despine(ax=ax, left=True, bottom=True)
plot_voight_painting(pr, palette=palette, flank='right', ax=ax)
# plot ehh
ax = fig.add_subplot(gs[1, 0])
sns.despine(ax=ax, offset=3)
x = np.arange(el.shape[0])
y = el
ax.fill_between(x, 0, y)
ax.set_ylim(0, 1)
ax.set_yticks([0, 1])
ax.set_ylabel('EHH')
ax.invert_xaxis()
ax = fig.add_subplot(gs[1, 1])
sns.despine(ax=ax, left=True, right=False, offset=3)
ax.yaxis.tick_right()
ax.set_ylim(0, 1)
ax.set_yticks([0, 1])
x = np.arange(er.shape[0])
y = er
ax.fill_between(x, 0, y)
# tidy up
fig.tight_layout()
return fig | python | def fig_voight_painting(h, index=None, palette='colorblind',
height_factor=0.01, fig=None):
import matplotlib.pyplot as plt
from matplotlib.gridspec import GridSpec
import seaborn as sns
# check inputs
h = asarray_ndim(h, 2)
if index is None:
# use midpoint
index = h.shape[0] // 2
# divide data into two flanks
hl = h[:index+1][::-1]
hr = h[index:]
# paint both flanks
pl, il = voight_painting(hl)
pr, ir = voight_painting(hr)
# compute ehh decay for both flanks
el = ehh_decay(hl, truncate=False)
er = ehh_decay(hr, truncate=False)
# setup figure
# fixed height for EHH decay subplot
h_ehh = plt.rcParams['figure.figsize'][1] // 3
# add height for paintings
h_painting = height_factor*h.shape[1]
if fig is None:
w = plt.rcParams['figure.figsize'][0]
h = h_ehh + h_painting
fig = plt.figure(figsize=(w, h))
# setup gridspec
gs = GridSpec(2, 2,
width_ratios=[hl.shape[0], hr.shape[0]],
height_ratios=[h_painting, h_ehh])
# plot paintings
ax = fig.add_subplot(gs[0, 0])
sns.despine(ax=ax, left=True, bottom=True)
plot_voight_painting(pl, palette=palette, flank='left', ax=ax)
ax = fig.add_subplot(gs[0, 1])
sns.despine(ax=ax, left=True, bottom=True)
plot_voight_painting(pr, palette=palette, flank='right', ax=ax)
# plot ehh
ax = fig.add_subplot(gs[1, 0])
sns.despine(ax=ax, offset=3)
x = np.arange(el.shape[0])
y = el
ax.fill_between(x, 0, y)
ax.set_ylim(0, 1)
ax.set_yticks([0, 1])
ax.set_ylabel('EHH')
ax.invert_xaxis()
ax = fig.add_subplot(gs[1, 1])
sns.despine(ax=ax, left=True, right=False, offset=3)
ax.yaxis.tick_right()
ax.set_ylim(0, 1)
ax.set_yticks([0, 1])
x = np.arange(er.shape[0])
y = er
ax.fill_between(x, 0, y)
# tidy up
fig.tight_layout()
return fig | [
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Parameters
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h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
index : int, optional
Index of the variant within the haplotype array to centre on. If not
provided, the middle variant will be used.
palette : string, optional
A Seaborn palette name.
height_factor : float, optional
If no axes provided, determine height of figure by multiplying
height of painting array by this number.
fig : figure
The figure on which to draw. If not provided, a new figure will be
created.
Returns
-------
fig : figure
Notes
-----
N.B., the ordering of haplotypes on the left and right flanks will be
different. This means that haplotypes on the right flank **will not**
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1,084 | cggh/scikit-allel | allel/stats/selection.py | compute_ihh_gaps | def compute_ihh_gaps(pos, map_pos, gap_scale, max_gap, is_accessible):
"""Compute spacing between variants for integrating haplotype
homozygosity.
Parameters
----------
pos : array_like, int, shape (n_variants,)
Variant positions (physical distance).
map_pos : array_like, float, shape (n_variants,)
Variant positions (genetic map distance).
gap_scale : int, optional
Rescale distance between variants if gap is larger than this value.
max_gap : int, optional
Do not report scores if EHH spans a gap larger than this number of
base pairs.
is_accessible : array_like, bool, optional
Genome accessibility array. If provided, distance between variants
will be computed as the number of accessible bases between them.
Returns
-------
gaps : ndarray, float, shape (n_variants - 1,)
"""
# check inputs
if map_pos is None:
# integrate over physical distance
map_pos = pos
else:
map_pos = asarray_ndim(map_pos, 1)
check_dim0_aligned(pos, map_pos)
# compute physical gaps
physical_gaps = np.diff(pos)
# compute genetic gaps
gaps = np.diff(map_pos).astype('f8')
if is_accessible is not None:
# compute accessible gaps
is_accessible = asarray_ndim(is_accessible, 1)
assert is_accessible.shape[0] > pos[-1], \
'accessibility array too short'
accessible_gaps = np.zeros_like(physical_gaps)
for i in range(1, len(pos)):
# N.B., expect pos is 1-based
n_access = np.count_nonzero(is_accessible[pos[i-1]-1:pos[i]-1])
accessible_gaps[i-1] = n_access
# adjust using accessibility
scaling = accessible_gaps / physical_gaps
gaps = gaps * scaling
elif gap_scale is not None and gap_scale > 0:
scaling = np.ones(gaps.shape, dtype='f8')
loc_scale = physical_gaps > gap_scale
scaling[loc_scale] = gap_scale / physical_gaps[loc_scale]
gaps = gaps * scaling
if max_gap is not None and max_gap > 0:
# deal with very large gaps
gaps[physical_gaps > max_gap] = -1
return gaps | python | def compute_ihh_gaps(pos, map_pos, gap_scale, max_gap, is_accessible):
# check inputs
if map_pos is None:
# integrate over physical distance
map_pos = pos
else:
map_pos = asarray_ndim(map_pos, 1)
check_dim0_aligned(pos, map_pos)
# compute physical gaps
physical_gaps = np.diff(pos)
# compute genetic gaps
gaps = np.diff(map_pos).astype('f8')
if is_accessible is not None:
# compute accessible gaps
is_accessible = asarray_ndim(is_accessible, 1)
assert is_accessible.shape[0] > pos[-1], \
'accessibility array too short'
accessible_gaps = np.zeros_like(physical_gaps)
for i in range(1, len(pos)):
# N.B., expect pos is 1-based
n_access = np.count_nonzero(is_accessible[pos[i-1]-1:pos[i]-1])
accessible_gaps[i-1] = n_access
# adjust using accessibility
scaling = accessible_gaps / physical_gaps
gaps = gaps * scaling
elif gap_scale is not None and gap_scale > 0:
scaling = np.ones(gaps.shape, dtype='f8')
loc_scale = physical_gaps > gap_scale
scaling[loc_scale] = gap_scale / physical_gaps[loc_scale]
gaps = gaps * scaling
if max_gap is not None and max_gap > 0:
# deal with very large gaps
gaps[physical_gaps > max_gap] = -1
return gaps | [
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Parameters
----------
pos : array_like, int, shape (n_variants,)
Variant positions (physical distance).
map_pos : array_like, float, shape (n_variants,)
Variant positions (genetic map distance).
gap_scale : int, optional
Rescale distance between variants if gap is larger than this value.
max_gap : int, optional
Do not report scores if EHH spans a gap larger than this number of
base pairs.
is_accessible : array_like, bool, optional
Genome accessibility array. If provided, distance between variants
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Returns
-------
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1,085 | cggh/scikit-allel | allel/stats/selection.py | xpnsl | def xpnsl(h1, h2, use_threads=True):
"""Cross-population version of the NSL statistic.
Parameters
----------
h1 : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array for the first population.
h2 : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array for the second population.
use_threads : bool, optional
If True use multiple threads to compute.
Returns
-------
score : ndarray, float, shape (n_variants,)
Unstandardized XPNSL scores.
"""
# check inputs
h1 = asarray_ndim(h1, 2)
check_integer_dtype(h1)
h2 = asarray_ndim(h2, 2)
check_integer_dtype(h2)
check_dim0_aligned(h1, h2)
h1 = memoryview_safe(h1)
h2 = memoryview_safe(h2)
if use_threads and multiprocessing.cpu_count() > 1:
# use multiple threads
# setup threadpool
pool = ThreadPool(min(4, multiprocessing.cpu_count()))
# scan forward
res1_fwd = pool.apply_async(nsl_scan, args=(h1,))
res2_fwd = pool.apply_async(nsl_scan, args=(h2,))
# scan backward
res1_rev = pool.apply_async(nsl_scan, args=(h1[::-1],))
res2_rev = pool.apply_async(nsl_scan, args=(h2[::-1],))
# wait for both to finish
pool.close()
pool.join()
# obtain results
nsl1_fwd = res1_fwd.get()
nsl2_fwd = res2_fwd.get()
nsl1_rev = res1_rev.get()
nsl2_rev = res2_rev.get()
# cleanup
pool.terminate()
else:
# compute without threads
# scan forward
nsl1_fwd = nsl_scan(h1)
nsl2_fwd = nsl_scan(h2)
# scan backward
nsl1_rev = nsl_scan(h1[::-1])
nsl2_rev = nsl_scan(h2[::-1])
# handle reverse scans
nsl1_rev = nsl1_rev[::-1]
nsl2_rev = nsl2_rev[::-1]
# compute unstandardized score
nsl1 = nsl1_fwd + nsl1_rev
nsl2 = nsl2_fwd + nsl2_rev
score = np.log(nsl1 / nsl2)
return score | python | def xpnsl(h1, h2, use_threads=True):
# check inputs
h1 = asarray_ndim(h1, 2)
check_integer_dtype(h1)
h2 = asarray_ndim(h2, 2)
check_integer_dtype(h2)
check_dim0_aligned(h1, h2)
h1 = memoryview_safe(h1)
h2 = memoryview_safe(h2)
if use_threads and multiprocessing.cpu_count() > 1:
# use multiple threads
# setup threadpool
pool = ThreadPool(min(4, multiprocessing.cpu_count()))
# scan forward
res1_fwd = pool.apply_async(nsl_scan, args=(h1,))
res2_fwd = pool.apply_async(nsl_scan, args=(h2,))
# scan backward
res1_rev = pool.apply_async(nsl_scan, args=(h1[::-1],))
res2_rev = pool.apply_async(nsl_scan, args=(h2[::-1],))
# wait for both to finish
pool.close()
pool.join()
# obtain results
nsl1_fwd = res1_fwd.get()
nsl2_fwd = res2_fwd.get()
nsl1_rev = res1_rev.get()
nsl2_rev = res2_rev.get()
# cleanup
pool.terminate()
else:
# compute without threads
# scan forward
nsl1_fwd = nsl_scan(h1)
nsl2_fwd = nsl_scan(h2)
# scan backward
nsl1_rev = nsl_scan(h1[::-1])
nsl2_rev = nsl_scan(h2[::-1])
# handle reverse scans
nsl1_rev = nsl1_rev[::-1]
nsl2_rev = nsl2_rev[::-1]
# compute unstandardized score
nsl1 = nsl1_fwd + nsl1_rev
nsl2 = nsl2_fwd + nsl2_rev
score = np.log(nsl1 / nsl2)
return score | [
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Parameters
----------
h1 : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array for the first population.
h2 : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array for the second population.
use_threads : bool, optional
If True use multiple threads to compute.
Returns
-------
score : ndarray, float, shape (n_variants,)
Unstandardized XPNSL scores. | [
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1,086 | cggh/scikit-allel | allel/stats/selection.py | haplotype_diversity | def haplotype_diversity(h):
"""Estimate haplotype diversity.
Parameters
----------
h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
Returns
-------
hd : float
Haplotype diversity.
"""
# check inputs
h = HaplotypeArray(h, copy=False)
# number of haplotypes
n = h.n_haplotypes
# compute haplotype frequencies
f = h.distinct_frequencies()
# estimate haplotype diversity
hd = (1 - np.sum(f**2)) * n / (n - 1)
return hd | python | def haplotype_diversity(h):
# check inputs
h = HaplotypeArray(h, copy=False)
# number of haplotypes
n = h.n_haplotypes
# compute haplotype frequencies
f = h.distinct_frequencies()
# estimate haplotype diversity
hd = (1 - np.sum(f**2)) * n / (n - 1)
return hd | [
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----------
h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
Returns
-------
hd : float
Haplotype diversity. | [
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1,087 | cggh/scikit-allel | allel/stats/selection.py | moving_haplotype_diversity | def moving_haplotype_diversity(h, size, start=0, stop=None, step=None):
"""Estimate haplotype diversity in moving windows.
Parameters
----------
h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
size : int
The window size (number of variants).
start : int, optional
The index at which to start.
stop : int, optional
The index at which to stop.
step : int, optional
The number of variants between start positions of windows. If not
given, defaults to the window size, i.e., non-overlapping windows.
Returns
-------
hd : ndarray, float, shape (n_windows,)
Haplotype diversity.
"""
hd = moving_statistic(values=h, statistic=haplotype_diversity, size=size,
start=start, stop=stop, step=step)
return hd | python | def moving_haplotype_diversity(h, size, start=0, stop=None, step=None):
hd = moving_statistic(values=h, statistic=haplotype_diversity, size=size,
start=start, stop=stop, step=step)
return hd | [
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Haplotype array.
size : int
The window size (number of variants).
start : int, optional
The index at which to start.
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The index at which to stop.
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The number of variants between start positions of windows. If not
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-------
hd : ndarray, float, shape (n_windows,)
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1,088 | cggh/scikit-allel | allel/stats/selection.py | plot_haplotype_frequencies | def plot_haplotype_frequencies(h, palette='Paired', singleton_color='w',
ax=None):
"""Plot haplotype frequencies.
Parameters
----------
h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
palette : string, optional
A Seaborn palette name.
singleton_color : string, optional
Color to paint singleton haplotypes.
ax : axes, optional
The axes on which to draw. If not provided, a new figure will be
created.
Returns
-------
ax : axes
"""
import matplotlib.pyplot as plt
import seaborn as sns
# check inputs
h = HaplotypeArray(h, copy=False)
# setup figure
if ax is None:
width = plt.rcParams['figure.figsize'][0]
height = width / 10
fig, ax = plt.subplots(figsize=(width, height))
sns.despine(ax=ax, left=True)
# count distinct haplotypes
hc = h.distinct_counts()
# setup palette
n_colors = np.count_nonzero(hc > 1)
palette = sns.color_palette(palette, n_colors)
# paint frequencies
x1 = 0
for i, c in enumerate(hc):
x2 = x1 + c
if c > 1:
color = palette[i]
else:
color = singleton_color
ax.axvspan(x1, x2, color=color)
x1 = x2
# tidy up
ax.set_xlim(0, h.shape[1])
ax.set_yticks([])
return ax | python | def plot_haplotype_frequencies(h, palette='Paired', singleton_color='w',
ax=None):
import matplotlib.pyplot as plt
import seaborn as sns
# check inputs
h = HaplotypeArray(h, copy=False)
# setup figure
if ax is None:
width = plt.rcParams['figure.figsize'][0]
height = width / 10
fig, ax = plt.subplots(figsize=(width, height))
sns.despine(ax=ax, left=True)
# count distinct haplotypes
hc = h.distinct_counts()
# setup palette
n_colors = np.count_nonzero(hc > 1)
palette = sns.color_palette(palette, n_colors)
# paint frequencies
x1 = 0
for i, c in enumerate(hc):
x2 = x1 + c
if c > 1:
color = palette[i]
else:
color = singleton_color
ax.axvspan(x1, x2, color=color)
x1 = x2
# tidy up
ax.set_xlim(0, h.shape[1])
ax.set_yticks([])
return ax | [
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Parameters
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h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
palette : string, optional
A Seaborn palette name.
singleton_color : string, optional
Color to paint singleton haplotypes.
ax : axes, optional
The axes on which to draw. If not provided, a new figure will be
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1,089 | cggh/scikit-allel | allel/stats/selection.py | moving_hfs_rank | def moving_hfs_rank(h, size, start=0, stop=None):
"""Helper function for plotting haplotype frequencies in moving windows.
Parameters
----------
h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
size : int
The window size (number of variants).
start : int, optional
The index at which to start.
stop : int, optional
The index at which to stop.
Returns
-------
hr : ndarray, int, shape (n_windows, n_haplotypes)
Haplotype rank array.
"""
# determine windows
windows = np.asarray(list(index_windows(h, size=size, start=start,
stop=stop, step=None)))
# setup output
hr = np.zeros((windows.shape[0], h.shape[1]), dtype='i4')
# iterate over windows
for i, (window_start, window_stop) in enumerate(windows):
# extract haplotypes for the current window
hw = h[window_start:window_stop]
# count haplotypes
hc = hw.distinct_counts()
# ensure sorted descending
hc.sort()
hc = hc[::-1]
# compute ranks for non-singleton haplotypes
cp = 0
for j, c in enumerate(hc):
if c > 1:
hr[i, cp:cp+c] = j+1
cp += c
return hr | python | def moving_hfs_rank(h, size, start=0, stop=None):
# determine windows
windows = np.asarray(list(index_windows(h, size=size, start=start,
stop=stop, step=None)))
# setup output
hr = np.zeros((windows.shape[0], h.shape[1]), dtype='i4')
# iterate over windows
for i, (window_start, window_stop) in enumerate(windows):
# extract haplotypes for the current window
hw = h[window_start:window_stop]
# count haplotypes
hc = hw.distinct_counts()
# ensure sorted descending
hc.sort()
hc = hc[::-1]
# compute ranks for non-singleton haplotypes
cp = 0
for j, c in enumerate(hc):
if c > 1:
hr[i, cp:cp+c] = j+1
cp += c
return hr | [
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Parameters
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h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
size : int
The window size (number of variants).
start : int, optional
The index at which to start.
stop : int, optional
The index at which to stop.
Returns
-------
hr : ndarray, int, shape (n_windows, n_haplotypes)
Haplotype rank array. | [
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1,090 | cggh/scikit-allel | allel/stats/selection.py | plot_moving_haplotype_frequencies | def plot_moving_haplotype_frequencies(pos, h, size, start=0, stop=None, n=None,
palette='Paired', singleton_color='w',
ax=None):
"""Plot haplotype frequencies in moving windows over the genome.
Parameters
----------
pos : array_like, int, shape (n_items,)
Variant positions, using 1-based coordinates, in ascending order.
h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
size : int
The window size (number of variants).
start : int, optional
The index at which to start.
stop : int, optional
The index at which to stop.
n : int, optional
Color only the `n` most frequent haplotypes (by default, all
non-singleton haplotypes are colored).
palette : string, optional
A Seaborn palette name.
singleton_color : string, optional
Color to paint singleton haplotypes.
ax : axes, optional
The axes on which to draw. If not provided, a new figure will be
created.
Returns
-------
ax : axes
"""
import matplotlib as mpl
import matplotlib.pyplot as plt
import seaborn as sns
# setup figure
if ax is None:
fig, ax = plt.subplots()
# compute haplotype frequencies
# N.B., here we use a haplotype rank data structure to enable the use of
# pcolormesh() which is a lot faster than any other type of plotting
# function
hr = moving_hfs_rank(h, size=size, start=start, stop=stop)
# truncate to n most common haplotypes
if n:
hr[hr > n] = 0
# compute window start and stop positions
windows = moving_statistic(pos, statistic=lambda v: (v[0], v[-1]),
size=size, start=start, stop=stop)
# create color map
colors = [singleton_color] + sns.color_palette(palette, n_colors=hr.max())
cmap = mpl.colors.ListedColormap(colors)
# draw colors
x = np.append(windows[:, 0], windows[-1, -1])
y = np.arange(h.shape[1]+1)
ax.pcolormesh(x, y, hr.T, cmap=cmap)
# tidy up
ax.set_xlim(windows[0, 0], windows[-1, -1])
ax.set_ylim(0, h.shape[1])
ax.set_ylabel('haplotype count')
ax.set_xlabel('position (bp)')
return ax | python | def plot_moving_haplotype_frequencies(pos, h, size, start=0, stop=None, n=None,
palette='Paired', singleton_color='w',
ax=None):
import matplotlib as mpl
import matplotlib.pyplot as plt
import seaborn as sns
# setup figure
if ax is None:
fig, ax = plt.subplots()
# compute haplotype frequencies
# N.B., here we use a haplotype rank data structure to enable the use of
# pcolormesh() which is a lot faster than any other type of plotting
# function
hr = moving_hfs_rank(h, size=size, start=start, stop=stop)
# truncate to n most common haplotypes
if n:
hr[hr > n] = 0
# compute window start and stop positions
windows = moving_statistic(pos, statistic=lambda v: (v[0], v[-1]),
size=size, start=start, stop=stop)
# create color map
colors = [singleton_color] + sns.color_palette(palette, n_colors=hr.max())
cmap = mpl.colors.ListedColormap(colors)
# draw colors
x = np.append(windows[:, 0], windows[-1, -1])
y = np.arange(h.shape[1]+1)
ax.pcolormesh(x, y, hr.T, cmap=cmap)
# tidy up
ax.set_xlim(windows[0, 0], windows[-1, -1])
ax.set_ylim(0, h.shape[1])
ax.set_ylabel('haplotype count')
ax.set_xlabel('position (bp)')
return ax | [
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pos : array_like, int, shape (n_items,)
Variant positions, using 1-based coordinates, in ascending order.
h : array_like, int, shape (n_variants, n_haplotypes)
Haplotype array.
size : int
The window size (number of variants).
start : int, optional
The index at which to start.
stop : int, optional
The index at which to stop.
n : int, optional
Color only the `n` most frequent haplotypes (by default, all
non-singleton haplotypes are colored).
palette : string, optional
A Seaborn palette name.
singleton_color : string, optional
Color to paint singleton haplotypes.
ax : axes, optional
The axes on which to draw. If not provided, a new figure will be
created.
Returns
-------
ax : axes | [
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1,091 | cggh/scikit-allel | allel/stats/selection.py | moving_delta_tajima_d | def moving_delta_tajima_d(ac1, ac2, size, start=0, stop=None, step=None):
"""Compute the difference in Tajima's D between two populations in
moving windows.
Parameters
----------
ac1 : array_like, int, shape (n_variants, n_alleles)
Allele counts array for the first population.
ac2 : array_like, int, shape (n_variants, n_alleles)
Allele counts array for the second population.
size : int
The window size (number of variants).
start : int, optional
The index at which to start.
stop : int, optional
The index at which to stop.
step : int, optional
The number of variants between start positions of windows. If not
given, defaults to the window size, i.e., non-overlapping windows.
Returns
-------
delta_d : ndarray, float, shape (n_windows,)
Standardized delta Tajima's D.
See Also
--------
allel.stats.diversity.moving_tajima_d
"""
d1 = moving_tajima_d(ac1, size=size, start=start, stop=stop, step=step)
d2 = moving_tajima_d(ac2, size=size, start=start, stop=stop, step=step)
delta = d1 - d2
delta_z = (delta - np.mean(delta)) / np.std(delta)
return delta_z | python | def moving_delta_tajima_d(ac1, ac2, size, start=0, stop=None, step=None):
d1 = moving_tajima_d(ac1, size=size, start=start, stop=stop, step=step)
d2 = moving_tajima_d(ac2, size=size, start=start, stop=stop, step=step)
delta = d1 - d2
delta_z = (delta - np.mean(delta)) / np.std(delta)
return delta_z | [
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ac1 : array_like, int, shape (n_variants, n_alleles)
Allele counts array for the first population.
ac2 : array_like, int, shape (n_variants, n_alleles)
Allele counts array for the second population.
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The window size (number of variants).
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The index at which to start.
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The index at which to stop.
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The number of variants between start positions of windows. If not
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Standardized delta Tajima's D.
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1,092 | cggh/scikit-allel | allel/stats/selection.py | make_similar_sized_bins | def make_similar_sized_bins(x, n):
"""Utility function to create a set of bins over the range of values in `x`
such that each bin contains roughly the same number of values.
Parameters
----------
x : array_like
The values to be binned.
n : int
The number of bins to create.
Returns
-------
bins : ndarray
An array of bin edges.
Notes
-----
The actual number of bins returned may be less than `n` if `x` contains
integer values and any single value is represented more than len(x)//n
times.
"""
# copy and sort the array
y = np.array(x).flatten()
y.sort()
# setup bins
bins = [y[0]]
# determine step size
step = len(y) // n
# add bin edges
for i in range(step, len(y), step):
# get value at this index
v = y[i]
# only add bin edge if larger than previous
if v > bins[-1]:
bins.append(v)
# fix last bin edge
bins[-1] = y[-1]
return np.array(bins) | python | def make_similar_sized_bins(x, n):
# copy and sort the array
y = np.array(x).flatten()
y.sort()
# setup bins
bins = [y[0]]
# determine step size
step = len(y) // n
# add bin edges
for i in range(step, len(y), step):
# get value at this index
v = y[i]
# only add bin edge if larger than previous
if v > bins[-1]:
bins.append(v)
# fix last bin edge
bins[-1] = y[-1]
return np.array(bins) | [
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n : int
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bins : ndarray
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Notes
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1,093 | cggh/scikit-allel | allel/stats/selection.py | standardize | def standardize(score):
"""Centre and scale to unit variance."""
score = asarray_ndim(score, 1)
return (score - np.nanmean(score)) / np.nanstd(score) | python | def standardize(score):
score = asarray_ndim(score, 1)
return (score - np.nanmean(score)) / np.nanstd(score) | [
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1,094 | cggh/scikit-allel | allel/stats/selection.py | standardize_by_allele_count | def standardize_by_allele_count(score, aac, bins=None, n_bins=None,
diagnostics=True):
"""Standardize `score` within allele frequency bins.
Parameters
----------
score : array_like, float
The score to be standardized, e.g., IHS or NSL.
aac : array_like, int
An array of alternate allele counts.
bins : array_like, int, optional
Allele count bins, overrides `n_bins`.
n_bins : int, optional
Number of allele count bins to use.
diagnostics : bool, optional
If True, plot some diagnostic information about the standardization.
Returns
-------
score_standardized : ndarray, float
Standardized scores.
bins : ndarray, int
Allele count bins used for standardization.
"""
from scipy.stats import binned_statistic
# check inputs
score = asarray_ndim(score, 1)
aac = asarray_ndim(aac, 1)
check_dim0_aligned(score, aac)
# remove nans
nonan = ~np.isnan(score)
score_nonan = score[nonan]
aac_nonan = aac[nonan]
if bins is None:
# make our own similar sized bins
# how many bins to make?
if n_bins is None:
# something vaguely reasonable
n_bins = np.max(aac) // 2
# make bins
bins = make_similar_sized_bins(aac_nonan, n_bins)
else:
# user-provided bins
bins = asarray_ndim(bins, 1)
mean_score, _, _ = binned_statistic(aac_nonan, score_nonan,
statistic=np.mean,
bins=bins)
std_score, _, _ = binned_statistic(aac_nonan, score_nonan,
statistic=np.std,
bins=bins)
if diagnostics:
import matplotlib.pyplot as plt
x = (bins[:-1] + bins[1:]) / 2
plt.figure()
plt.fill_between(x,
mean_score - std_score,
mean_score + std_score,
alpha=.5,
label='std')
plt.plot(x, mean_score, marker='o', label='mean')
plt.grid(axis='y')
plt.xlabel('Alternate allele count')
plt.ylabel('Unstandardized score')
plt.title('Standardization diagnostics')
plt.legend()
# apply standardization
score_standardized = np.empty_like(score)
for i in range(len(bins) - 1):
x1 = bins[i]
x2 = bins[i + 1]
if i == 0:
# first bin
loc = (aac < x2)
elif i == len(bins) - 2:
# last bin
loc = (aac >= x1)
else:
# middle bins
loc = (aac >= x1) & (aac < x2)
m = mean_score[i]
s = std_score[i]
score_standardized[loc] = (score[loc] - m) / s
return score_standardized, bins | python | def standardize_by_allele_count(score, aac, bins=None, n_bins=None,
diagnostics=True):
from scipy.stats import binned_statistic
# check inputs
score = asarray_ndim(score, 1)
aac = asarray_ndim(aac, 1)
check_dim0_aligned(score, aac)
# remove nans
nonan = ~np.isnan(score)
score_nonan = score[nonan]
aac_nonan = aac[nonan]
if bins is None:
# make our own similar sized bins
# how many bins to make?
if n_bins is None:
# something vaguely reasonable
n_bins = np.max(aac) // 2
# make bins
bins = make_similar_sized_bins(aac_nonan, n_bins)
else:
# user-provided bins
bins = asarray_ndim(bins, 1)
mean_score, _, _ = binned_statistic(aac_nonan, score_nonan,
statistic=np.mean,
bins=bins)
std_score, _, _ = binned_statistic(aac_nonan, score_nonan,
statistic=np.std,
bins=bins)
if diagnostics:
import matplotlib.pyplot as plt
x = (bins[:-1] + bins[1:]) / 2
plt.figure()
plt.fill_between(x,
mean_score - std_score,
mean_score + std_score,
alpha=.5,
label='std')
plt.plot(x, mean_score, marker='o', label='mean')
plt.grid(axis='y')
plt.xlabel('Alternate allele count')
plt.ylabel('Unstandardized score')
plt.title('Standardization diagnostics')
plt.legend()
# apply standardization
score_standardized = np.empty_like(score)
for i in range(len(bins) - 1):
x1 = bins[i]
x2 = bins[i + 1]
if i == 0:
# first bin
loc = (aac < x2)
elif i == len(bins) - 2:
# last bin
loc = (aac >= x1)
else:
# middle bins
loc = (aac >= x1) & (aac < x2)
m = mean_score[i]
s = std_score[i]
score_standardized[loc] = (score[loc] - m) / s
return score_standardized, bins | [
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score : array_like, float
The score to be standardized, e.g., IHS or NSL.
aac : array_like, int
An array of alternate allele counts.
bins : array_like, int, optional
Allele count bins, overrides `n_bins`.
n_bins : int, optional
Number of allele count bins to use.
diagnostics : bool, optional
If True, plot some diagnostic information about the standardization.
Returns
-------
score_standardized : ndarray, float
Standardized scores.
bins : ndarray, int
Allele count bins used for standardization. | [
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1,095 | cggh/scikit-allel | allel/stats/window.py | moving_statistic | def moving_statistic(values, statistic, size, start=0, stop=None, step=None, **kwargs):
"""Calculate a statistic in a moving window over `values`.
Parameters
----------
values : array_like
The data to summarise.
statistic : function
The statistic to compute within each window.
size : int
The window size (number of values).
start : int, optional
The index at which to start.
stop : int, optional
The index at which to stop.
step : int, optional
The distance between start positions of windows. If not given,
defaults to the window size, i.e., non-overlapping windows.
kwargs
Additional keyword arguments are passed through to the `statistic`
function.
Returns
-------
out : ndarray, shape (n_windows,)
Examples
--------
>>> import allel
>>> values = [2, 5, 8, 16]
>>> allel.moving_statistic(values, np.sum, size=2)
array([ 7, 24])
>>> allel.moving_statistic(values, np.sum, size=2, step=1)
array([ 7, 13, 24])
"""
windows = index_windows(values, size, start, stop, step)
# setup output
out = np.array([statistic(values[i:j], **kwargs) for i, j in windows])
return out | python | def moving_statistic(values, statistic, size, start=0, stop=None, step=None, **kwargs):
windows = index_windows(values, size, start, stop, step)
# setup output
out = np.array([statistic(values[i:j], **kwargs) for i, j in windows])
return out | [
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The data to summarise.
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The statistic to compute within each window.
size : int
The window size (number of values).
start : int, optional
The index at which to start.
stop : int, optional
The index at which to stop.
step : int, optional
The distance between start positions of windows. If not given,
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kwargs
Additional keyword arguments are passed through to the `statistic`
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Returns
-------
out : ndarray, shape (n_windows,)
Examples
--------
>>> import allel
>>> values = [2, 5, 8, 16]
>>> allel.moving_statistic(values, np.sum, size=2)
array([ 7, 24])
>>> allel.moving_statistic(values, np.sum, size=2, step=1)
array([ 7, 13, 24]) | [
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1,096 | cggh/scikit-allel | allel/stats/window.py | window_locations | def window_locations(pos, windows):
"""Locate indices in `pos` corresponding to the start and stop positions
of `windows`.
"""
start_locs = np.searchsorted(pos, windows[:, 0])
stop_locs = np.searchsorted(pos, windows[:, 1], side='right')
locs = np.column_stack((start_locs, stop_locs))
return locs | python | def window_locations(pos, windows):
start_locs = np.searchsorted(pos, windows[:, 0])
stop_locs = np.searchsorted(pos, windows[:, 1], side='right')
locs = np.column_stack((start_locs, stop_locs))
return locs | [
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1,097 | cggh/scikit-allel | allel/stats/window.py | per_base | def per_base(x, windows, is_accessible=None, fill=np.nan):
"""Calculate the per-base value of a windowed statistic.
Parameters
----------
x : array_like, shape (n_windows,)
The statistic to average per-base.
windows : array_like, int, shape (n_windows, 2)
The windows used, as an array of (window_start, window_stop)
positions using 1-based coordinates.
is_accessible : array_like, bool, shape (len(contig),), optional
Boolean array indicating accessibility status for all positions in the
chromosome/contig.
fill : object, optional
Use this value where there are no accessible bases in a window.
Returns
-------
y : ndarray, float, shape (n_windows,)
The input array divided by the number of (accessible) bases in each
window.
n_bases : ndarray, int, shape (n_windows,)
The number of (accessible) bases in each window
"""
# calculate window sizes
if is_accessible is None:
# N.B., window stops are included
n_bases = np.diff(windows, axis=1).reshape(-1) + 1
else:
n_bases = np.array([np.count_nonzero(is_accessible[i-1:j])
for i, j in windows])
# deal with multidimensional x
if x.ndim == 1:
pass
elif x.ndim == 2:
n_bases = n_bases[:, None]
else:
raise NotImplementedError('only arrays of 1 or 2 dimensions supported')
# calculate density per-base
with ignore_invalid():
y = np.where(n_bases > 0, x / n_bases, fill)
# restore to 1-dimensional
if n_bases.ndim > 1:
n_bases = n_bases.reshape(-1)
return y, n_bases | python | def per_base(x, windows, is_accessible=None, fill=np.nan):
# calculate window sizes
if is_accessible is None:
# N.B., window stops are included
n_bases = np.diff(windows, axis=1).reshape(-1) + 1
else:
n_bases = np.array([np.count_nonzero(is_accessible[i-1:j])
for i, j in windows])
# deal with multidimensional x
if x.ndim == 1:
pass
elif x.ndim == 2:
n_bases = n_bases[:, None]
else:
raise NotImplementedError('only arrays of 1 or 2 dimensions supported')
# calculate density per-base
with ignore_invalid():
y = np.where(n_bases > 0, x / n_bases, fill)
# restore to 1-dimensional
if n_bases.ndim > 1:
n_bases = n_bases.reshape(-1)
return y, n_bases | [
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] | Calculate the per-base value of a windowed statistic.
Parameters
----------
x : array_like, shape (n_windows,)
The statistic to average per-base.
windows : array_like, int, shape (n_windows, 2)
The windows used, as an array of (window_start, window_stop)
positions using 1-based coordinates.
is_accessible : array_like, bool, shape (len(contig),), optional
Boolean array indicating accessibility status for all positions in the
chromosome/contig.
fill : object, optional
Use this value where there are no accessible bases in a window.
Returns
-------
y : ndarray, float, shape (n_windows,)
The input array divided by the number of (accessible) bases in each
window.
n_bases : ndarray, int, shape (n_windows,)
The number of (accessible) bases in each window | [
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] | 3c979a57a100240ba959dd13f98839349530f215 | https://github.com/cggh/scikit-allel/blob/3c979a57a100240ba959dd13f98839349530f215/allel/stats/window.py#L379-L431 |
1,098 | cggh/scikit-allel | allel/stats/window.py | equally_accessible_windows | def equally_accessible_windows(is_accessible, size, start=0, stop=None, step=None):
"""Create windows each containing the same number of accessible bases.
Parameters
----------
is_accessible : array_like, bool, shape (n_bases,)
Array defining accessible status of all bases on a contig/chromosome.
size : int
Window size (number of accessible bases).
start : int, optional
The genome position at which to start.
stop : int, optional
The genome position at which to stop.
step : int, optional
The number of accessible sites between start positions
of windows. If not given, defaults to the window size, i.e.,
non-overlapping windows. Use half the window size to get
half-overlapping windows.
Returns
-------
windows : ndarray, int, shape (n_windows, 2)
Window start/stop positions (1-based).
"""
pos_accessible, = np.nonzero(is_accessible)
pos_accessible += 1 # convert to 1-based coordinates
# N.B., need some care in handling start and stop positions, these are
# genomic positions at which to start and stop the windows
if start:
pos_accessible = pos_accessible[pos_accessible >= start]
if stop:
pos_accessible = pos_accessible[pos_accessible <= stop]
# now construct moving windows
windows = moving_statistic(pos_accessible, lambda v: [v[0], v[-1]],
size=size, step=step)
return windows | python | def equally_accessible_windows(is_accessible, size, start=0, stop=None, step=None):
pos_accessible, = np.nonzero(is_accessible)
pos_accessible += 1 # convert to 1-based coordinates
# N.B., need some care in handling start and stop positions, these are
# genomic positions at which to start and stop the windows
if start:
pos_accessible = pos_accessible[pos_accessible >= start]
if stop:
pos_accessible = pos_accessible[pos_accessible <= stop]
# now construct moving windows
windows = moving_statistic(pos_accessible, lambda v: [v[0], v[-1]],
size=size, step=step)
return windows | [
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Parameters
----------
is_accessible : array_like, bool, shape (n_bases,)
Array defining accessible status of all bases on a contig/chromosome.
size : int
Window size (number of accessible bases).
start : int, optional
The genome position at which to start.
stop : int, optional
The genome position at which to stop.
step : int, optional
The number of accessible sites between start positions
of windows. If not given, defaults to the window size, i.e.,
non-overlapping windows. Use half the window size to get
half-overlapping windows.
Returns
-------
windows : ndarray, int, shape (n_windows, 2)
Window start/stop positions (1-based). | [
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] | 3c979a57a100240ba959dd13f98839349530f215 | https://github.com/cggh/scikit-allel/blob/3c979a57a100240ba959dd13f98839349530f215/allel/stats/window.py#L434-L472 |
1,099 | bartTC/django-attachments | attachments/templatetags/attachments_tags.py | attachment_form | def attachment_form(context, obj):
"""
Renders a "upload attachment" form.
The user must own ``attachments.add_attachment permission`` to add
attachments.
"""
if context['user'].has_perm('attachments.add_attachment'):
return {
'form': AttachmentForm(),
'form_url': add_url_for_obj(obj),
'next': context.request.build_absolute_uri(),
}
else:
return {'form': None} | python | def attachment_form(context, obj):
if context['user'].has_perm('attachments.add_attachment'):
return {
'form': AttachmentForm(),
'form_url': add_url_for_obj(obj),
'next': context.request.build_absolute_uri(),
}
else:
return {'form': None} | [
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The user must own ``attachments.add_attachment permission`` to add
attachments. | [
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] | 012b7168f9342e07683a54ceab57696e0072962e | https://github.com/bartTC/django-attachments/blob/012b7168f9342e07683a54ceab57696e0072962e/attachments/templatetags/attachments_tags.py#L12-L26 |
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