def write_output_file(metric_file_data, output_dir, metric, all_samples):
# now have matrix where output_row is rarefaction analysis
metric_file_data = sorted(metric_file_data,key=operator.itemgetter(1,2))
row_names = [row.pop(0) for row in metric_file_data]
col_names = ['sequences per sample', 'iteration'] + all_samples
#Numpy shows weird behaviour when converting metric_file_data to array
#it truncates some values, so better go with straight list of lists
# format_matrix() now takes 2d lists as well as arrays.
out_str = format_matrix(metric_file_data, row_names, col_names)
f = open(os.path.join(output_dir,metric+'.txt'),'w')
f.write(out_str)
f.close()
def write_output_file(metric_file_data, output_dir, metric, all_samples):
# now have matrix where output_row is rarefaction analysis
metric_file_data = sorted(metric_file_data,key=operator.itemgetter(1,2))
row_names = [row.pop(0) for row in metric_file_data]
col_names = ['sequences per sample', 'iteration'] + all_samples
#Numpy shows weird behaviour when converting metric_file_data to array
#it truncates some values, so better go with straight list of lists
# format_matrix() now takes 2d lists as well as arrays.
out_str = format_matrix(metric_file_data, row_names, col_names)
f = open(os.path.join(output_dir,metric+'.txt'),'w')
f.write(out_str)
f.close()
def test_format_matrix(self):
"""format_matrix should return tab-delimited mat"""
a = [[1, 2, 3], [4, 5, 6], [7, 8, 9]]
row_labels = ["a", "b", "c"]
col_labels = [11, 22, 33]
res = format_matrix(a, row_labels, col_labels)
# test as list
self.assertEqual(res, "\t11\t22\t33\na\t1\t2\t3\nb\t4\t5\t6\nc\t7\t8\t9")
self.assertRaises(ValueError, format_matrix, a, row_labels[:2], col_labels)
self.assertRaises(ValueError, format_matrix, None, row_labels, col_labels)
# tes as array
a = array(a)
self.assertEqual(res, "\t11\t22\t33\na\t1\t2\t3\nb\t4\t5\t6\nc\t7\t8\t9")
self.assertRaises(ValueError, format_matrix, a, row_labels[:2], col_labels)
self.assertRaises(ValueError, format_matrix, None, row_labels, col_labels)
def test_format_matrix(self):
"""format_matrix should return tab-delimited mat"""
a = [[1,2,3], [4,5,6], [7,8,9]]
row_labels = ['a','b','c']
col_labels = [11,22,33]
res = format_matrix(a, row_labels, col_labels)
#test as list
self.assertEqual(res,
'\t11\t22\t33\na\t1\t2\t3\nb\t4\t5\t6\nc\t7\t8\t9')
self.assertRaises(ValueError, format_matrix, a, row_labels[:2], col_labels)
self.assertRaises(ValueError, format_matrix, None, row_labels, col_labels)
#tes as array
a = array(a)
self.assertEqual(res,
'\t11\t22\t33\na\t1\t2\t3\nb\t4\t5\t6\nc\t7\t8\t9')
self.assertRaises(ValueError, format_matrix, a, row_labels[:2], col_labels)
self.assertRaises(ValueError, format_matrix, None, row_labels, col_labels)
def single_object_beta(otu_table, metrics, tr, rowids=None, full_tree=False):
"""mod of single_file_beta to recieve and return otu obj, tree str
uses name in metrics to name output beta diversity files
assumes input tree is already trimmed to contain only otus present
in otu_table, doesn't call getSubTree()
inputs:
otu_table -- a otu_table in the biom format
metrics -- metrics (str, comma delimited if more than 1 metric)
tr -- a phylonode cogent tree object if needed by the chosen beta
diversity metric
rowids -- comma seperated string
"""
if isinstance(otu_table, DenseTable):
otumtx = otu_table._data.T
else:
otumtx = asarray([v for v in otu_table.iterSampleData()])
if tr:
tree = tr
else:
tree = None
metrics_list = metrics.split(',')
for metric in metrics_list:
try:
metric_f = get_nonphylogenetic_metric(metric)
is_phylogenetic = False
except AttributeError:
try:
metric_f = get_phylogenetic_metric(metric)
is_phylogenetic = True
if tree is None:
stderr.write(
"metric %s requires a tree, but none found\n" %
(metric, ))
exit(1)
except AttributeError:
stderr.write(
"Could not find metric %s.\n\nKnown metrics are: %s\n" %
(metric, ', '.join(list_known_metrics())))
exit(1)
if rowids is None:
# standard, full way
if is_phylogenetic:
dissims = metric_f(otumtx,
otu_table.ObservationIds,
tree,
otu_table.SampleIds,
make_subtree=(not full_tree))
else:
dissims = metric_f(otumtx)
return (format_distance_matrix(otu_table.SampleIds,
dissims).split('\n'))
else:
# only calc d(rowid1, *) for each rowid
rowids_list = rowids.split(',')
row_dissims = [] # same order as rowids_list
for rowid in rowids_list:
rowidx = otu_table.SampleIds.index(rowid)
# first test if we can the dissim is a fn of only the pair
# if not, just calc the whole matrix
if metric_f.__name__ == 'dist_chisq' or \
metric_f.__name__ == 'dist_gower' or \
metric_f.__name__ == 'dist_hellinger' or\
metric_f.__name__ == 'binary_dist_chisq':
warnings.warn(
'dissimilarity ' + metric_f.__name__ +
' is not parallelized, calculating the whole matrix...'
)
row_dissims.append(metric_f(otumtx)[rowidx])
else:
try:
row_metric = get_phylogenetic_row_metric(metric)
except AttributeError:
# do element by element
dissims = []
for i in range(len(otu_table.SampleIds)):
if is_phylogenetic:
dissim = metric_f(
otumtx[[rowidx, i], :],
otu_table.ObservationIds,
tree, [
otu_table.SampleIds[rowidx],
otu_table.SampleIds[i]
],
make_subtree=(not full_tree))[0, 1]
else:
dissim = metric_f(otumtx[[rowidx, i], :])[0, 1]
dissims.append(dissim)
row_dissims.append(dissims)
else:
# do whole row at once
dissims = row_metric(otumtx,
otu_table.ObservationIds,
tree,
otu_table.SampleIds,
rowid,
make_subtree=(not full_tree))
row_dissims.append(dissims)
return format_matrix(row_dissims, rowids_list, otu_table.SampleIds)
def single_file_beta(input_path,
metrics,
tree_path,
output_dir,
rowids=None,
full_tree=False):
""" does beta diversity calc on a single otu table
uses name in metrics to name output beta diversity files
assumes input tree is already trimmed to contain only otus present in otu
table, doesn't call getSubTree()
inputs:
input_path (str)
metrics (str, comma delimited if more than 1 metric; or list)
tree_path (str)
output_dir (str)
rowids (comma separated str)
"""
metrics_list = metrics
try:
metrics_list = metrics_list.split(',')
except AttributeError:
pass
otu_table = parse_biom_table(open(input_path, 'U'))
if isinstance(otu_table, DenseTable):
otumtx = otu_table._data.T
else:
otumtx = asarray([v for v in otu_table.iterSampleData()])
if tree_path:
tree = parse_newick(open(tree_path, 'U'), PhyloNode)
else:
tree = None
input_dir, input_filename = os.path.split(input_path)
input_basename, input_ext = os.path.splitext(input_filename)
for metric in metrics_list:
outfilepath = os.path.join(output_dir,
metric + '_' + input_basename + '.txt')
try:
metric_f = get_nonphylogenetic_metric(metric)
is_phylogenetic = False
except AttributeError:
try:
metric_f = get_phylogenetic_metric(metric)
is_phylogenetic = True
if tree is None:
stderr.write(
"metric %s requires a tree, but none found\n" %
(metric, ))
exit(1)
except AttributeError:
stderr.write(
"Could not find metric %s.\n\nKnown metrics are: %s\n" %
(metric, ', '.join(list_known_metrics())))
exit(1)
if rowids is None:
# standard, full way
if is_phylogenetic:
dissims = metric_f(otumtx,
otu_table.ObservationIds,
tree,
otu_table.SampleIds,
make_subtree=(not full_tree))
else:
dissims = metric_f(otumtx)
f = open(outfilepath, 'w')
f.write(format_distance_matrix(otu_table.SampleIds, dissims))
f.close()
else:
# only calc d(rowid1, *) for each rowid
rowids_list = rowids.split(',')
row_dissims = [] # same order as rowids_list
for rowid in rowids_list:
rowidx = otu_table.SampleIds.index(rowid)
# first test if we can the dissim is a fn of only the pair
# if not, just calc the whole matrix
if metric_f.__name__ == 'dist_chisq' or \
metric_f.__name__ == 'dist_gower' or \
metric_f.__name__ == 'dist_hellinger' or\
metric_f.__name__ == 'binary_dist_chisq':
warnings.warn(
'dissimilarity ' + metric_f.__name__ +
' is not parallelized, calculating the whole matrix...'
)
row_dissims.append(metric_f(otumtx)[rowidx])
else:
try:
row_metric = get_phylogenetic_row_metric(metric)
except AttributeError:
# do element by element
dissims = []
for i in range(len(otu_table.SampleIds)):
if is_phylogenetic:
dissim = metric_f(
otumtx[[rowidx, i], :],
otu_table.ObservationIds,
tree, [
otu_table.SampleIds[rowidx],
otu_table.SampleIds[i]
],
make_subtree=(not full_tree))[0, 1]
else:
dissim = metric_f(otumtx[[rowidx, i], :])[0, 1]
dissims.append(dissim)
row_dissims.append(dissims)
else:
# do whole row at once
dissims = row_metric(otumtx,
otu_table.ObservationIds,
tree,
otu_table.SampleIds,
rowid,
make_subtree=(not full_tree))
row_dissims.append(dissims)
# rows_outfilepath = os.path.join(output_dir, metric + '_' +\
# '_'.join(rowids_list) + '_' + os.path.split(input_path)[1])
f = open(outfilepath, 'w')
f.write(
format_matrix(row_dissims, rowids_list, otu_table.SampleIds))
f.close()
def single_object_beta(otu_table, metrics, tr, rowids=None,
full_tree=False):
"""mod of single_file_beta to recieve and return otu obj, tree str
uses name in metrics to name output beta diversity files
assumes input tree is already trimmed to contain only otus present
in otu_table, doesn't call getSubTree()
inputs:
otu_table -- a otu_table in the biom format
metrics -- metrics (str, comma delimited if more than 1 metric)
tr -- a phylonode cogent tree object if needed by the chosen beta
diversity metric
rowids -- comma seperated string
"""
if isinstance(otu_table, DenseTable):
otumtx = otu_table._data.T
else:
otumtx = asarray([v for v in otu_table.iterSampleData()])
if tr:
tree = tr
else:
tree = None
metrics_list = metrics.split(',')
for metric in metrics_list:
try:
metric_f = get_nonphylogenetic_metric(metric)
is_phylogenetic = False
except AttributeError:
try:
metric_f = get_phylogenetic_metric(metric)
is_phylogenetic = True
if tree == None:
stderr.write("metric %s requires a tree, but none found\n"\
% (metric,))
exit(1)
except AttributeError:
stderr.write("Could not find metric %s.\n\nKnown metrics are: %s\n"\
% (metric, ', '.join(list_known_metrics())))
exit(1)
if rowids == None:
# standard, full way
if is_phylogenetic:
dissims = metric_f(otumtx, otu_table.ObservationIds, tree,
otu_table.SampleIds, make_subtree = (not full_tree))
else:
dissims = metric_f(otumtx)
return format_distance_matrix(otu_table.SampleIds, dissims).split('\n')
else:
# only calc d(rowid1, *) for each rowid
rowids_list = rowids.split(',')
row_dissims = [] # same order as rowids_list
for rowid in rowids_list:
rowidx = otu_table.SampleIds.index(rowid)
# first test if we can the dissim is a fn of only the pair
# if not, just calc the whole matrix
if metric_f.__name__ == 'dist_chisq' or \
metric_f.__name__ == 'dist_gower' or \
metric_f.__name__ == 'dist_hellinger' or\
metric_f.__name__ == 'binary_dist_chisq':
warnings.warn('dissimilarity '+metric_f.__name__+\
' is not parallelized, calculating the whole matrix...')
row_dissims.append(metric_f(otumtx)[rowidx])
else:
try:
row_metric = get_phylogenetic_row_metric(metric)
except AttributeError:
# do element by element
dissims = []
for i in range(len(otu_table.SampleIds)):
if is_phylogenetic:
dissim = metric_f(otumtx[[rowidx,i],:],
otu_table.ObservationIds, tree,
[otu_table.SampleIds[rowidx],
otu_table.SampleIds[i]],
make_subtree = (not full_tree))[0,1]
else:
dissim = metric_f(otumtx[[rowidx,i],:])[0,1]
dissims.append(dissim)
row_dissims.append(dissims)
else:
# do whole row at once
dissims = row_metric(otumtx,
otu_table.ObservationIds, tree,
otu_table.SampleIds, rowid,
make_subtree = (not full_tree))
row_dissims.append(dissims)
return format_matrix(row_dissims,rowids_list,otu_table.SampleIds)
def single_file_beta(input_path, metrics, tree_path, output_dir,
rowids=None, full_tree=False):
""" does beta diversity calc on a single otu table
uses name in metrics to name output beta diversity files
assumes input tree is already trimmed to contain only otus present in otu
table, doesn't call getSubTree()
inputs:
input_path (str)
metrics (str, comma delimited if more than 1 metric; or list)
tree_path (str)
output_dir (str)
rowids (comma separated str)
"""
metrics_list = metrics
try:
metrics_list = metrics_list.split(',')
except AttributeError:
pass
otu_table = parse_biom_table(open(input_path,'U'))
if isinstance(otu_table, DenseTable):
otumtx = otu_table._data.T
else:
otumtx = asarray([v for v in otu_table.iterSampleData()])
if tree_path:
tree = parse_newick(open(tree_path, 'U'),
PhyloNode)
else:
tree = None
input_dir, input_filename = os.path.split(input_path)
input_basename, input_ext = os.path.splitext(input_filename)
for metric in metrics_list:
outfilepath = os.path.join(output_dir, metric + '_' + \
input_basename + '.txt')
try:
metric_f = get_nonphylogenetic_metric(metric)
is_phylogenetic = False
except AttributeError:
try:
metric_f = get_phylogenetic_metric(metric)
is_phylogenetic = True
if tree == None:
stderr.write("metric %s requires a tree, but none found\n"\
% (metric,))
exit(1)
except AttributeError:
stderr.write("Could not find metric %s.\n\nKnown metrics are: %s\n"\
% (metric, ', '.join(list_known_metrics())))
exit(1)
if rowids == None:
# standard, full way
if is_phylogenetic:
dissims = metric_f(otumtx, otu_table.ObservationIds, \
tree, otu_table.SampleIds, make_subtree = (not full_tree))
else:
dissims = metric_f(otumtx)
f = open(outfilepath,'w')
f.write(format_distance_matrix(otu_table.SampleIds, dissims))
f.close()
else:
# only calc d(rowid1, *) for each rowid
rowids_list = rowids.split(',')
row_dissims = [] # same order as rowids_list
for rowid in rowids_list:
rowidx = otu_table.SampleIds.index(rowid)
# first test if we can the dissim is a fn of only the pair
# if not, just calc the whole matrix
if metric_f.__name__ == 'dist_chisq' or \
metric_f.__name__ == 'dist_gower' or \
metric_f.__name__ == 'dist_hellinger' or\
metric_f.__name__ == 'binary_dist_chisq':
warnings.warn('dissimilarity '+metric_f.__name__+\
' is not parallelized, calculating the whole matrix...')
row_dissims.append(metric_f(otumtx)[rowidx])
else:
try:
row_metric = get_phylogenetic_row_metric(metric)
except AttributeError:
# do element by element
dissims = []
for i in range(len(otu_table.SampleIds)):
if is_phylogenetic:
dissim = metric_f(otumtx[[rowidx,i],:],
otu_table.ObservationIds, tree,
[otu_table.SampleIds[rowidx],
otu_table.SampleIds[i]],
make_subtree = (not full_tree))[0,1]
else:
dissim = metric_f(otumtx[[rowidx,i],:])[0,1]
dissims.append(dissim)
row_dissims.append(dissims)
else:
# do whole row at once
dissims = row_metric(otumtx,
otu_table.ObservationIds, tree,
otu_table.SampleIds, rowid,
make_subtree = (not full_tree))
row_dissims.append(dissims)
# rows_outfilepath = os.path.join(output_dir, metric + '_' +\
# '_'.join(rowids_list) + '_' + os.path.split(input_path)[1])
f = open(outfilepath,'w')
f.write(format_matrix(row_dissims,rowids_list,otu_table.SampleIds))
f.close()
def formatResult(self, result):
"""Generate formatted distance - result is (data, sample_names)"""
data, sample_names, calc_names = result
res = format_matrix(data, sample_names, calc_names)
return res
def formatResult(self, result):
"""Generate formatted distance - result is (data, sample_names)"""
data, sample_names, calc_names = result
res = format_matrix(data, sample_names, calc_names)
return res
def single_file_beta(input_path,
metrics,
tree_path,
output_dir,
rowids=None,
full_tree=False):
""" does beta diversity calc on a single otu table
uses name in metrics to name output beta diversity files
assumes input tree is already trimmed to contain only otus present in otu
table, doesn't call getSubTree()
inputs:
input_path (str)
metrics (str, comma delimited if more than 1 metric)
tree_path (str)
output_dir (str)
rowids (comma separated str)
"""
f = open(input_path, 'U')
samids, otuids, otumtx, lineages = parse_otu_table(f)
# otu mtx is otus by samples
f.close()
tree = None
if tree_path:
f = open(tree_path, 'U')
tree = parse_newick(f, PhyloNode)
f.close()
if not full_tree:
tree = tree.getSubTree(otuids, ignore_missing=True)
metrics_list = metrics.split(',')
for metric in metrics_list:
outfilepath = os.path.join(output_dir,
metric + '_' + os.path.split(input_path)[1])
try:
metric_f = get_nonphylogenetic_metric(metric)
is_phylogenetic = False
except AttributeError:
try:
metric_f = get_phylogenetic_metric(metric)
is_phylogenetic = True
if tree == None:
stderr.write("metric %s requires a tree, but none found\n"\
% (metric,))
exit(1)
except AttributeError:
stderr.write("Could not find metric %s.\n\nKnown metrics are: %s\n"\
% (metric, ', '.join(list_known_metrics())))
exit(1)
if rowids == None:
# standard, full way
if is_phylogenetic:
dissims = metric_f(otumtx.T, otuids, tree, samids)
else:
dissims = metric_f(otumtx.T)
f = open(outfilepath, 'w')
f.write(format_distance_matrix(samids, dissims))
f.close()
else:
# only calc d(rowid1, *) for each rowid
rowids_list = rowids.split(',')
row_dissims = [] # same order as rowids_list
for rowid in rowids_list:
rowidx = samids.index(rowid)
# first test if we can the dissim is a fn of only the pair
# if not, just calc the whole matrix
if metric_f.__name__ == 'dist_chisq' or \
metric_f.__name__ == 'dist_gower' or \
metric_f.__name__ == 'dist_hellinger' or\
metric_f.__name__ == 'binary_dist_chisq':
row_dissims.append(metric_f(otumtx.T)[rowidx])
else:
try:
row_metric = get_phylogenetic_row_metric(metric)
except AttributeError:
# do element by element
dissims = []
for i in range(len(samids)):
if is_phylogenetic:
dissim = metric_f(
otumtx.T[[rowidx, i], :], otuids, tree,
[samids[rowidx], samids[i]])[0, 1]
else:
dissim = metric_f(otumtx.T[[rowidx, i], :])[0,
1]
dissims.append(dissim)
row_dissims.append(dissims)
else:
# do whole row at once
dissims = row_metric(otumtx.T, otuids, tree, samids,
rowid)
row_dissims.append(dissims)
# rows_outfilepath = os.path.join(output_dir, metric + '_' +\
# '_'.join(rowids_list) + '_' + os.path.split(input_path)[1])
f = open(outfilepath, 'w')
f.write(format_matrix(row_dissims, rowids_list, samids))
f.close()