def write_biom(self, sample_names, read_taxonomies, biom_file_io):
'''Write the OTU info to a biom IO output stream
Parameters
----------
sample_names: String
names of each sample (sample_ids for biom)
read_taxonomies: Array of hashes as per _iterate_otu_table_rows()
biom_file_io: io
open writeable stream to write biom contents to
Returns True if successful, else False'''
counts = []
observ_metadata = []
otu_ids = []
for otu_id, tax, count in self._iterate_otu_table_rows(read_taxonomies):
if len(count) != len(sample_names):
raise Exception("Programming error: mismatched sample names and counts")
counts.append(count)
observ_metadata.append({'taxonomy': tax})
otu_ids.append(str(otu_id))
if len(counts) == 0:
logging.info("Not writing BIOM file since no sequences were assigned taxonomy")
return True
table = Table(np.array(counts),
otu_ids, sample_names, observ_metadata,
[{}]*len(sample_names), table_id='GraftM Taxonomy Count Table')
try:
table.to_hdf5(biom_file_io, 'GraftM graft')
return True
except RuntimeError as e:
logging.warn("Error writing BIOM output, file not written. The specific error was: %s" % e)
return False
def load_BIOM(table, informat='json', v=1):
"""
load a BIOM table from BIOM format. Default format is 'json'.
"""
from biom.table import Table
import json
import sys
informats = ['json','tsv']
if not informat in informats:
print "\nPlease specify a valid BIOM input format. Currently we support: '%s'.\n" %"', '".join(informats)
else:
if v:
print "\nSpecified BIOM input format '%s' - ok!" %(informat)
if informat == 'json':
with open(table) as data_file:
data = json.load(data_file)
t = Table.from_json(data)
elif informat == 'tsv':
tsv = open(in_tsv)
func = lambda x : x
t = Table.from_tsv(tsv, obs_mapping=None, sample_mapping=None, process_func=func)
tsv.close()
return t
def setUp(self):
"""define some top-level data"""
self.otu_table_values = array([[0, 0, 9, 5, 3, 1], [1, 5, 4, 0, 3, 2], [2, 3, 1, 1, 2, 5]])
{
(0, 2): 9.0,
(0, 3): 5.0,
(0, 4): 3.0,
(0, 5): 1.0,
(1, 0): 1.0,
(1, 1): 5.0,
(1, 2): 4.0,
(1, 4): 3.0,
(1, 5): 2.0,
(2, 0): 2.0,
(2, 1): 3.0,
(2, 2): 1.0,
(2, 3): 1.0,
(2, 4): 2.0,
(2, 5): 5.0,
}
self.otu_table = Table(
self.otu_table_values,
["OTU1", "OTU2", "OTU3"],
["Sample1", "Sample2", "Sample3", "Sample4", "Sample5", "Sample6"],
[{"taxonomy": ["Bacteria"]}, {"taxonomy": ["Archaea"]}, {"taxonomy": ["Streptococcus"]}],
[None, None, None, None, None, None],
)
self.otu_table_f = Table(
self.otu_table_values,
["OTU1", "OTU2", "OTU3"],
["Sample1", "Sample2", "Sample3", "Sample4", "Sample5", "Sample6"],
[
{"taxonomy": ["1A", "1B", "1C", "Bacteria"]},
{"taxonomy": ["2A", "2B", "2C", "Archaea"]},
{"taxonomy": ["3A", "3B", "3C", "Streptococcus"]},
],
[None, None, None, None, None, None],
)
self.full_lineages = [
["1A", "1B", "1C", "Bacteria"],
["2A", "2B", "2C", "Archaea"],
["3A", "3B", "3C", "Streptococcus"],
]
self.metadata = [
[
["Sample1", "NA", "A"],
["Sample2", "NA", "B"],
["Sample3", "NA", "A"],
["Sample4", "NA", "B"],
["Sample5", "NA", "A"],
["Sample6", "NA", "B"],
],
["SampleID", "CAT1", "CAT2"],
[],
]
self.tree_text = ["('OTU3',('OTU1','OTU2'))"]
fh, self.tmp_heatmap_fpath = mkstemp(prefix="test_heatmap_", suffix=".pdf")
close(fh)
def test_tree_filter_table_none(self):
rooted_nwk = io.StringIO("(O1:4.5,(O2:4,(a:1,b:1):2):0.5);")
tree = skbio.TreeNode.read(rooted_nwk)
table = Table(np.array([[0, 1, 3], [1, 1, 2]]),
['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_table(table, tree)
expected = table.filter(['O1', 'O2'], axis='observation')
self.assertEqual(actual, expected)
def parse_biom_table(fp, input_is_dense=False):
try:
return Table.from_hdf5(fp)
except:
pass
if hasattr(fp, 'read'):
return Table.from_json(json.load(fp), input_is_dense=input_is_dense)
elif isinstance(fp, list):
return Table.from_json(json.loads(''.join(fp)),
input_is_dense=input_is_dense)
else:
return Table.from_json(json.loads(fp), input_is_dense=input_is_dense)
def BIOM_return_clipped_taxonomy(taxlevel, BIOM):
"""
Returns a BIOM table for which the taxonomy has been clipped at a certain level
"""
from biom.table import Table
import numpy as np
return_OTUs = {}
levels = ['kingdom', 'phylum', 'class', 'order', 'family', 'genus', 'species', 'unassigned']
clip_level=''
to_drop=[]
if not taxlevel in levels:
raise KeyError("The taxonomic level you are trying to search: '%s', is not valid" %level)
clip_level = int(levels.index(taxlevel))+1
#check if the first OTU has 'taxonomy' metadata attached, if yes assume all others have too and resume
if not 'taxonomy' in BIOM.metadata(axis='observation')[0]:
raise KeyError('The BIOM table you are trying to screen does not have taxonomy metadata attached to it')
else:
print "Found taxonomy metadata with OTUs - ok!"
sample_ids = BIOM.ids(axis='sample')
observation_ids = BIOM.ids(axis='observation')
data_to_biom = []
sample_metadata = BIOM.metadata(axis='sample')
observation_metadata = BIOM.metadata(axis='observation')
for OTU in observation_ids:
orig=BIOM.data(OTU, axis='observation')
data_to_biom.append(orig)
data = np.asarray(data_to_biom)
for i in range(len(observation_metadata)):
if len(observation_metadata[i]['taxonomy']) > clip_level:
observation_metadata[i]['taxonomy'] = observation_metadata[i]['taxonomy'][:clip_level]
if 'unknown' in observation_metadata[i]['taxonomy'][-1]:
print "fishy: %s" %observation_metadata[i]['taxonomy']
to_drop.append(observation_ids[i])
# print observation_metadata[i]['taxonomy']
#construct adjusted table
outtable = Table(data, observation_ids, sample_ids, table_id='OTU table', sample_metadata=sample_metadata, observation_metadata=observation_metadata)
if to_drop:
outtable.filter(to_drop, invert=True, axis='observation',inplace=True)
return outtable
def BIOM_tsv_to_R_transpose(in_tsv, out_csv):
"""
Parse a biom table in tsv format and transpose it for input into R
"""
from biom import Table
tsv = open(in_tsv)
#in_tsv = open('COI-trim30min100-merge-c3-id97-OTU-taxonomy.kraken.tsv')
func = lambda x : x
intable = Table.from_tsv(tsv,obs_mapping=None, sample_mapping=None, process_func=func)
outtable = intable.transpose()
out=open("transposed.tsv","w")
out.write(outtable.to_tsv(header_key=None, header_value=None))
out.close()
#refine
intable = open('transposed.tsv','r')
temp = intable.next()
out=''
for line in intable:
if line.startswith('#'):
if line.strip().endswith('taxomomy'):
print "Removing taxonomy"
line = ",".join(line.strip().split("\t")[:-1]).replace('#OTU ID','Sample').replace('\t',',')+'\n'
line = line.replace('#OTU ID','Sample').replace('\t',',')
out+=line
else:
line = line.replace('\t',',')
out+=line
outtable = open(out_csv,'w')
outtable.write(out)
outtable.close()
def setUp(self):
self.otu_table_vals = array([[1, 0, 2, 4],
[1, 2, 0, 1],
[0, 1, 1, 0],
[1, 2, 1, 0]])
self.otu_table = Table(self.otu_table_vals,
['0', '1', '2', '3'],
['s1', 's2', 's3', 's4'],
[{"taxonomy": ["Root", "Bacteria", "Actinobacteria", "Actinobacteria", "Coriobacteridae", "Coriobacteriales", "Coriobacterineae", "Coriobacteriaceae"]},
{"taxonomy": ["Root",
"Bacteria",
"Firmicutes",
"\"Clostridia\""]},
{"taxonomy": ["Root",
"Bacteria",
"Firmicutes",
"\"Clostridia\""]},
{"taxonomy": ["Root", "Bacteria"]}],
None,)
self.mapping = """#SampleID\tBarcodeSequence\tTreatment\tDescription
#Test mapping file
s1\tAAAA\tControl\tControl mouse, I.D. 354
s2\tGGGG\tControl\tControl mouse, I.D. 355
s3\tCCCC\tExp\tDisease mouse, I.D. 356
s4\tTTTT\tExp\tDisease mouse, I.D. 357""".split('\n')
def run(self, **kwargs):
json_table_str = kwargs['json_table_str']
hdf5_biom = kwargs['hdf5_table']
axis = kwargs['axis']
ids = kwargs['ids']
if axis not in self.Axes:
raise CommandError("Invalid axis '%s'. Must be either %s." % (
axis,
' or '.join(map(lambda e: "'%s'" % e, self.Axes))))
if hdf5_biom is None and json_table_str is None:
raise CommandError("Must specify an input table")
elif hdf5_biom is not None and json_table_str is not None:
raise CommandError("Can only specify one input table")
if json_table_str is not None:
idxs, new_axis_md = get_axis_indices(json_table_str, ids, axis)
new_data = direct_slice_data(json_table_str, idxs, axis)
# multiple walks over the string. bad form, but easy right now
# ...should add a yield_and_ignore parser or something.
def subset_generator():
yield "{"
yield direct_parse_key(json_table_str, "id")
yield ","
yield direct_parse_key(json_table_str, "format")
yield ","
yield direct_parse_key(json_table_str, "format_url")
yield ","
yield direct_parse_key(json_table_str, "type")
yield ","
yield direct_parse_key(json_table_str, "generated_by")
yield ","
yield direct_parse_key(json_table_str, "date")
yield ","
yield direct_parse_key(json_table_str, "matrix_type")
yield ","
yield direct_parse_key(json_table_str, "matrix_element_type")
yield ","
yield new_data
yield ","
yield new_axis_md
yield ","
if axis == "observation":
yield direct_parse_key(json_table_str, "columns")
else:
yield direct_parse_key(json_table_str, "rows")
yield "}"
format_ = 'json'
table = subset_generator()
else:
with biom_open(hdf5_biom) as f:
table = Table.from_hdf5(f, ids=ids, axis=axis)
format_ = 'hdf5'
return {'subsetted_table': (table, format_)}
def filter_BIOM_by_per_sample_read_prop(BIOM, min_prop=0.01):
"""
Filter OTU table by mininimum reads per sample
"""
import numpy as np
from biom.table import Table
print "\nFiltering at level: %s %%\n" %(min_prop*100)
# print "input table:\n"
# print BIOM
# print "\n"
sample_ids = BIOM.ids(axis='sample')
observation_ids = BIOM.ids(axis='observation')
data_to_biom = []
sample_metadata = BIOM.metadata(axis='sample')
observation_metadata = BIOM.metadata(axis='observation')
sums = BIOM.sum(axis='sample')
for OTU in observation_ids:
orig=BIOM.data(OTU, axis='observation')
for i in range(len(orig)):
if not int(orig[i]) == 0:
if not int(orig[i]) >= sums[i]*min_prop:
orig[i] = '0.0'
data_to_biom.append(orig)
data = np.asarray(data_to_biom)
#construct adjusted table
table = Table(data, observation_ids, sample_ids, table_id='OTU table', sample_metadata=sample_metadata, observation_metadata=observation_metadata)
#Filter OTUs with sum = '0'
to_exclude = []
observation_sums = table.sum(axis='observation')
for i in range(len(observation_sums)):
if int(observation_sums[i]) == 0:
to_exclude.append(observation_ids[i])
print "Removing %i OTUs for lack of support\n" %len(to_exclude)
table.filter(to_exclude, invert=True, axis='observation',inplace=True)
# print table
return table
def main(table_loc, otu_list, collapsed_name, output_file, classic=False):
table = load_table(table_loc)
f = open(otu_list)
otus = f.read().strip().split()
otus = set(otus) & set(table.ids(axis="observation"))
table1 = table.filter(otus, axis="observation", inplace=False)
table2 = table.filter(otus, axis="observation", invert=True, inplace=False)
sums1 = table1.sum(axis='sample')
sums2 = table2.sum(axis='sample')
new_table = Table(numpy.array([sums1,sums2]), [collapsed_name, "not_"+collapsed_name], table.ids(axis="sample"), type="otu baptable")
if classic:
# print to tab delimited biom table
open(output_file, 'w').write(new_table.to_tsv())
else:
# print biom table
new_table.to_json("predict_reactions.py", open(output_file, 'w'))
def build_OTU_table_biom(OTU_table_classic, OTU_table_biom, dataset_ID):
# Builds a BIOM format OTU table from an OTU table in classic dense format (sample IDs in the first row, OTU IDs in the first column). For some reason, 'biom convert' command fails to recognize some OTU tables, and therefore the method classic2biom (above) fails.
with open(OTU_table_classic,'r') as fidin:
otu_table_data = fidin.readlines()
firstrow = otu_table_data[0].split('\t')
sample_labels = firstrow[1:]
sample_labels[len(sample_labels)-1] = sample_labels[len(sample_labels)-1].rstrip('\n')
OTU_labels = [otu_table_data[i].split('\t')[0] for i in range(1,len(otu_table_data))]
nOTUs = len(OTU_labels)
nSamples = len(sample_labels)
# Load OTU table row major order
OTU_table_data = np.zeros((nOTUs, nSamples))
for i in range(1,nOTUs+1):
OTU_table_data[i-1,:] = otu_table_data[i].split('\t')[1:]
# Write in BIOM format
t = Table(OTU_table_data, OTU_labels, sample_labels, observ_metadata=None, sample_metadata=None, table_id=dataset_ID)
with biom_open(OTU_table_biom, 'w') as f:
t.to_hdf5(f, "Generated by processing layer", compress=False)
def setUp(self):
"""define some top-level data"""
self.otu_table_values = array([[0, 0, 9, 5, 3, 1],
[1, 5, 4, 0, 3, 2],
[2, 3, 1, 1, 2, 5]])
{(0, 2): 9.0, (0, 3): 5.0, (0, 4): 3.0, (0, 5): 1.0,
(1, 0): 1.0, (1, 1): 5.0, (1, 2): 4.0, (1, 4): 3.0, (1, 5): 2.0,
(2, 0): 2.0, (2, 1): 3.0, (2, 2): 1.0, (2, 3): 1.0, (2, 4): 2.0, (2, 5): 5.0}
self.otu_table = Table(self.otu_table_values,
['OTU1', 'OTU2', 'OTU3'],
['Sample1', 'Sample2', 'Sample3',
'Sample4', 'Sample5', 'Sample6'],
[{"taxonomy": ['Bacteria']},
{"taxonomy": ['Archaea']},
{"taxonomy": ['Streptococcus']}],
[None, None, None, None, None, None])
self.otu_table_f = Table(self.otu_table_values,
['OTU1', 'OTU2', 'OTU3'],
['Sample1', 'Sample2', 'Sample3',
'Sample4', 'Sample5', 'Sample6'],
[{"taxonomy": ['1A', '1B', '1C', 'Bacteria']},
{"taxonomy":
['2A', '2B', '2C', 'Archaea']},
{"taxonomy": ['3A', '3B', '3C', 'Streptococcus']}],
[None, None, None, None, None, None])
self.full_lineages = [['1A', '1B', '1C', 'Bacteria'],
['2A', '2B', '2C', 'Archaea'],
['3A', '3B', '3C', 'Streptococcus']]
self.metadata = [[['Sample1', 'NA', 'A'],
['Sample2', 'NA', 'B'],
['Sample3', 'NA', 'A'],
['Sample4', 'NA', 'B'],
['Sample5', 'NA', 'A'],
['Sample6', 'NA', 'B']],
['SampleID', 'CAT1', 'CAT2'], []]
self.tree_text = ["('OTU3',('OTU1','OTU2'))"]
fh, self.tmp_heatmap_fpath = mkstemp(prefix='test_heatmap_',
suffix='.pdf')
close(fh)
def convert_table_to_biom(table_f, sample_mapping, obs_mapping,
process_func, **kwargs):
"""Convert a contigency table to a biom table
sample_mapping : dict of {'sample_id':metadata} or None
obs_mapping : dict of {'obs_id':metadata} or None
process_func: a function to transform observation metadata
dtype : type of table data
"""
otu_table = Table.from_tsv(table_f, obs_mapping, sample_mapping,
process_func, **kwargs)
return otu_table.to_json(generatedby())
def _subset_table(hdf5_biom, json_table_str, axis, ids):
if axis not in ['sample', 'observation']:
raise ValueError("Invalid axis '%s'. Must be either 'sample' or "
"'observation'." % axis)
if hdf5_biom is None and json_table_str is None:
raise ValueError("Must specify an input table")
elif hdf5_biom is not None and json_table_str is not None:
raise ValueError("Can only specify one input table")
if json_table_str is not None:
idxs, new_axis_md = get_axis_indices(json_table_str, ids, axis)
new_data = direct_slice_data(json_table_str, idxs, axis)
# multiple walks over the string. bad form, but easy right now
# ...should add a yield_and_ignore parser or something.
def subset_generator():
yield "{"
yield direct_parse_key(json_table_str, "id")
yield ","
yield direct_parse_key(json_table_str, "format")
yield ","
yield direct_parse_key(json_table_str, "format_url")
yield ","
yield direct_parse_key(json_table_str, "type")
yield ","
yield direct_parse_key(json_table_str, "generated_by")
yield ","
yield direct_parse_key(json_table_str, "date")
yield ","
yield direct_parse_key(json_table_str, "matrix_type")
yield ","
yield direct_parse_key(json_table_str, "matrix_element_type")
yield ","
yield new_data
yield ","
yield new_axis_md
yield ","
if axis == "observation":
yield direct_parse_key(json_table_str, "columns")
else:
yield direct_parse_key(json_table_str, "rows")
yield "}"
format_ = 'json'
table = subset_generator()
else:
with biom_open(hdf5_biom) as f:
table = Table.from_hdf5(f, ids=ids, axis=axis)
format_ = 'hdf5'
return table, format_
def test_aitchison(self):
t = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = beta(table=t, metric='aitchison')
expected = skbio.DistanceMatrix([[0.0000000, 0.4901290, 0.6935510],
[0.4901290, 0.0000000, 0.2034219],
[0.6935510, 0.2034219, 0.0000000]],
ids=['S1', 'S2', 'S3'])
self.assertEqual(actual.ids, expected.ids)
for id1 in actual.ids:
for id2 in actual.ids:
npt.assert_almost_equal(actual[id1, id2], expected[id1, id2])
def simulate_correls(corr_stren=(.99, .99), std=(1, 1, 1, 2, 2), means=(100, 100, 100, 100, 100), size=30,
noncors=10, noncors_mean=100, noncors_std=100):
"""
Generates a correlation matrix with diagonal of stds based on input parameters and fills rest of matrix with
uncorrelated values all with same mean and standard deviations. Output should have a triangle of correlated
observations and a pair all other observations should be uncorrelated. Correlation to covariance calculated by
cor(X,Y)=cov(X,Y)/sd(X)sd(Y).
Parameters
----------
corr_stren: tuple of length 2, correlations in triangle and in pair
std: tuple of length 5, standard deviations of each observation
means: tuple of length 5, mean of each observation
size: number of samples to generate from the multivariate normal distribution
noncors: number of uncorrelated values
noncors_mean: mean of uncorrelated values
noncors_std: standard deviation of uncorrelated values
Returns
-------
table: a biom table with (size) samples and (5+noncors) observations
"""
cor = [[std[0], corr_stren[0], corr_stren[0], 0., 0.], # define the correlation matrix for the triangle and pair
[corr_stren[0], std[1], corr_stren[0], 0., 0.],
[corr_stren[0], corr_stren[0], std[2], 0., 0.],
[0., 0., 0., std[3], corr_stren[1]],
[0., 0., 0., corr_stren[1], std[4]]]
cor = np.array(cor)
cov = np.zeros(np.array(cor.shape) + noncors) # generate empty covariance matrix to be filled
for i in range(cor.shape[0]): # fill in all but diagonal of covariance matrix, first 5
for j in range(i + 1, cor.shape[0]):
curr_cov = cor[i, j] * cor[i, i] * cor[j, j]
cov[i, j] = curr_cov
cov[j, i] = curr_cov
for i in range(cor.shape[0]): # fill diagonal of covariance matrix, first 5
cov[i, i] = np.square(cor[i, i])
means = list(means)
for i in range(cor.shape[0], cov.shape[0]): # fill diagonal of covariance, 6 to end and populate mean list
cov[i, i] = noncors_std
means.append(noncors_mean)
# fill the count table
counts = multivariate_normal(means, cov, size).T
counts = np.round(counts)
observ_ids = ["Observ_" + str(i) for i in range(cov.shape[0])]
sample_ids = ["Sample_" + str(i) for i in range(size)]
table = Table(counts, observ_ids, sample_ids)
return table
def test_feature_metadata(self):
# no filtering
df = pd.DataFrame({'SequencedGenome': ['yes', 'yes']},
index=pd.Index(['O1', 'O2'], name='id'))
metadata = qiime2.Metadata(df)
table = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_features(table, metadata=metadata)
expected = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
self.assertEqual(actual, expected)
# filter one
df = pd.DataFrame({'SequencedGenome': ['yes']},
index=pd.Index(['O1'], name='id'))
metadata = qiime2.Metadata(df)
table = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_features(table, metadata=metadata)
expected = Table(np.array([[1, 3]]), ['O1'], ['S2', 'S3'])
self.assertEqual(actual, expected)
# filter all
df = pd.DataFrame({}, index=pd.Index(['foo'], name='id'))
metadata = qiime2.Metadata(df)
table = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_features(table, metadata=metadata)
self.assertTrue(actual.is_empty())
# exclude one
df = pd.DataFrame({'SequencedGenome': ['yes']},
index=pd.Index(['O1'], name='id'))
metadata = qiime2.Metadata(df)
table = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_features(table, metadata=metadata, exclude_ids=True)
expected = Table(np.array([[1, 1, 2]]), ['O2'], ['S1', 'S2', 'S3'])
self.assertEqual(actual, expected)
# exclude all
df = pd.DataFrame({'SequencedGenome': ['yes', 'yes']},
index=pd.Index(['O1', 'O2'], name='id'))
metadata = qiime2.Metadata(df)
table = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_features(table, metadata=metadata, exclude_ids=True)
self.assertTrue(actual.is_empty())
def test_where(self):
# no filtering
df = pd.DataFrame({'SequencedGenome': ['yes', 'no']},
index=pd.Index(['O1', 'O2'], name='feature-id'))
metadata = qiime2.Metadata(df)
table = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
where = "SequencedGenome='yes' OR SequencedGenome='no'"
actual = filter_features(table, metadata=metadata, where=where)
expected = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
self.assertEqual(actual, expected)
# filter one
df = pd.DataFrame({'SequencedGenome': ['yes', 'no']},
index=pd.Index(['O1', 'O2'], name='feature-id'))
metadata = qiime2.Metadata(df)
table = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
where = "SequencedGenome='yes'"
actual = filter_features(table, metadata=metadata, where=where)
expected = Table(np.array([[1, 3]]), ['O1'], ['S2', 'S3'])
self.assertEqual(actual, expected)
# filter all
df = pd.DataFrame({'SequencedGenome': ['yes', 'no']},
index=pd.Index(['O1', 'O2'], name='feature-id'))
metadata = qiime2.Metadata(df)
table = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
where = "SequencedGenome='yes' AND SequencedGenome='no'"
actual = filter_features(table, metadata=metadata, where=where)
expected = Table(np.array([]), [], [])
self.assertEqual(actual, expected)
# filter one -> exclude one
df = pd.DataFrame({'SequencedGenome': ['yes', 'no']},
index=pd.Index(['O1', 'O2'], name='feature-id'))
metadata = qiime2.Metadata(df)
table = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
where = "SequencedGenome='yes'"
actual = filter_features(table,
exclude_ids=True,
metadata=metadata,
where=where)
expected = Table(np.array([[1, 1, 2]]), ['O2'], ['S1', 'S2', 'S3'])
self.assertEqual(actual, expected)
def test_invalid_args(self):
table = Table(np.array([[0, 1, 3], [1, 1, 2]]),
['O1', 'O2'],
['S1', 'S2', 'S3'])
with self.assertRaisesRegex(ValueError, "No filtering"):
filter_samples(table)
with self.assertRaisesRegex(ValueError,
"'where' is specified."):
filter_samples(table, where="Subject='subject-1'")
with self.assertRaisesRegex(ValueError,
"'exclude_ids' is True."):
filter_samples(table, exclude_ids=True)
def test_non_phylogenetic(self):
t = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = beta_diversity('braycurtis', t)
# expected computed with scipy.spatial.distance.braycurtis
expected = skbio.DistanceMatrix([[0.0000000, 0.3333333, 0.6666667],
[0.3333333, 0.0000000, 0.4285714],
[0.6666667, 0.4285714, 0.0000000]],
ids=['S1', 'S2', 'S3'])
self.assertEqual(actual.ids, expected.ids)
for id1 in actual.ids:
for id2 in actual.ids:
npt.assert_almost_equal(actual[id1, id2], expected[id1, id2])
def fastspar_correlation(table: Table,
verbose: bool = False,
nprocs=1) -> pd.DataFrame:
# TODO: multiprocess support
with tempfile.TemporaryDirectory(prefix='fastspar') as temp:
table.to_dataframe().to_dense().to_csv(path.join(
temp, 'otu_table.tsv'),
sep='\t',
index_label='#OTU ID')
if verbose:
stdout = None
else:
stdout = subprocess.DEVNULL
subprocess.run([
'fastspar', '-c',
path.join(temp, 'otu_table.tsv'), '-r',
path.join(temp, path.join(temp, 'correl_table.tsv')), '-a',
path.join(temp, 'covar_table.tsv'), '-t',
str(nprocs)
],
stdout=stdout)
cor = pd.read_table(path.join(temp, 'correl_table.tsv'), index_col=0)
return df_to_correls(cor)
def generaete_biom_file(res_df, o, tg_rank, sampleid):
"""
output result in biom format
"""
import numpy as np
import biom
from biom.table import Table
if biom.__version__ < '2.1.7':
sys.exit("[ERROR] Biom library requires v2.1.7 or above.\n")
target_df = pd.DataFrame()
target_idx = (res_df['LEVEL']==tg_rank)
target_df = res_df.loc[target_idx, ['ABUNDANCE','TAXID']]
target_df['LINEAGE'] = target_df['TAXID'].apply(lambda x: gt.taxid2lineage(x, True, True)).str.split('|')
sample_ids = [sampleid]
data = np.array(target_df['ABUNDANCE']).reshape(len(target_df), 1)
observ_ids = target_df['TAXID']
observ_metadata = [{'taxonomy': x} for x in target_df['LINEAGE'].tolist()]
biom_table = Table(data, observ_ids, sample_ids, observ_metadata, table_id='GOTTCHA2')
biom_table.to_json('GOTTCHA2', direct_io=o)
return True
def test_rarefy_to_files2(self):
"""rarefy_to_files should write valid files with some metadata on otus
"""
maker = RarefactionMaker(self.otu_table_meta_fp, 0, 1, 1, 1)
maker.rarefy_to_files(self.rare_dir,
include_full=True,
include_lineages=False)
fname = os.path.join(self.rare_dir, "rarefaction_1_0.biom")
with biom_open(fname, 'U') as biom_file:
otu_table = Table.from_hdf5(biom_file)
self.assertItemsEqual(otu_table.ids(), self.otu_table.ids()[:2])
def make_modules_on_correlations(correlation_table: pd.DataFrame, feature_table: Table, min_r: float=.35) -> \
(Table, nx.Graph, pd.Series):
modules = ma.make_modules_naive(correlation_table, min_r=min_r)
modules_rev = {asv: module for module, asvs in modules.items() for asv in asvs}
for asv in feature_table.ids(axis='observation'):
if asv not in modules_rev:
modules_rev[asv] = None
module_membership = pd.Series(modules_rev)
coll_table = ma.collapse_modules(feature_table, modules)
metadata = get_metadata_from_table(feature_table)
metadata = ma.add_modules_to_metadata(modules, metadata)
correlation_table_filtered = filter_correls(correlation_table, conet=True, min_r=min_r)
net = correls_to_net(correlation_table_filtered, metadata=metadata)
return coll_table, net, module_membership
def test_beta_jensenshannon(self):
t = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = beta(table=t, metric='jensenshannon')
# expected computed with scipy.spatial.distance.jensenshannon
expected = skbio.DistanceMatrix([[0.0000000, 0.4645014, 0.52379239],
[0.4645014, 0.0000000, 0.07112939],
[0.52379239, 0.07112939, 0.0000000]],
ids=['S1', 'S2', 'S3'])
self.assertEqual(actual.ids, expected.ids)
for id1 in actual.ids:
for id2 in actual.ids:
npt.assert_almost_equal(actual[id1, id2], expected[id1, id2])
def test_beta_canberra_adkins(self):
t = Table(np.array([[0, 0], [0, 1], [1, 2]]),
['O1', 'O2', 'O3'],
['S1', 'S2'])
d = (1. / 2.) * sum([abs(0. - 1.) / (0. + 1.),
abs(1. - 2.) / (1. + 2.)])
expected = skbio.DistanceMatrix(np.array([[0.0, d], [d, 0.0]]),
ids=['S1', 'S2'])
actual = beta(table=t, metric='canberra_adkins')
self.assertEqual(actual.ids, expected.ids)
for id1 in actual.ids:
for id2 in actual.ids:
npt.assert_almost_equal(actual[id1, id2], expected[id1, id2])
def setUp(self):
THIS_DIR = os.path.dirname(os.path.abspath(__file__))
tablefp = Table({}, [], [])
self.emptyfeatures = tablefp
goodtable = os.path.join(THIS_DIR, 'data/features_formated.biom')
self.features = load_table(goodtable)
goodtable = os.path.join(THIS_DIR, 'data/features2_formated.biom')
ms2_match = os.path.join(THIS_DIR, 'data/ms2_match.txt')
self.ms2_match = pd.read_csv(ms2_match, sep='\t', index_col=0)
self.features2 = load_table(goodtable)
self.goodcsi = qiime2.Artifact.load(os.path.join(THIS_DIR,
'data/csiFolder.qza'))
self.goodcsi2 = qiime2.Artifact.load(os.path.join(
THIS_DIR, 'data/csiFolder2.qza'))
def calculate_correlations(table: Table, corr_method: str='spearman',
p_adjustment_method: str='fdr_bh') -> pd.DataFrame:
# TODO: multiprocess this
corr_method_fun = correl_methods[corr_method]
correls = pd.DataFrame(index=['r', 'p'])
for (val_i, id_i, _), (val_j, id_j, _) in table.iter_pairwise(axis='observation'):
r, p = corr_method_fun(val_i, val_j)
correls[id_i, id_j] = r, p
correls = correls.transpose()
correls.index = pd.MultiIndex.from_tuples(correls.index) # Turn tuple index into actual multiindex
if p_adjustment_method is not None:
correls['p_adjusted'] = p_adjust(correls.p, method=p_adjustment_method)
correls = correls.sort_values('p')
return correls
def test_combine_id_and_frequency_filters(self):
# no filtering
df = pd.DataFrame(
{
'Subject': ['subject-1', 'subject-1', 'subject-2'],
'SampleType': ['gut', 'tongue', 'gut']
},
index=pd.Index(['S1', 'S2', 'S3'], name='#SampleID'))
metadata = qiime2.Metadata(df)
table = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
where = "Subject='subject-1' OR Subject='subject-2'"
actual = filter_samples(table,
metadata=metadata,
where=where,
min_frequency=1)
expected = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
self.assertEqual(actual, expected)
# id and frequency filters active
df = pd.DataFrame(
{
'Subject': ['subject-1', 'subject-1', 'subject-2'],
'SampleType': ['gut', 'tongue', 'gut']
},
index=pd.Index(['S1', 'S2', 'S3'], name='#SampleID'))
metadata = qiime2.Metadata(df)
table = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
where = "Subject='subject-1'"
actual = filter_samples(table,
metadata=metadata,
where=where,
min_frequency=2)
expected = Table(np.array([[1], [1]]), ['O1', 'O2'], ['S2'])
self.assertEqual(actual, expected)
def write_biom(self, sample_names, read_taxonomies, biom_file_io):
'''Write the OTU info to a biom IO output stream
Parameters
----------
sample_names: String
names of each sample (sample_ids for biom)
read_taxonomies: Array of hashes as per _iterate_otu_table_rows()
biom_file_io: io
open writeable stream to write biom contents to
Returns True if successful, else False'''
counts = []
observ_metadata = []
otu_ids = []
for otu_id, tax, count in self._iterate_otu_table_rows(
read_taxonomies):
if len(count) != len(sample_names):
raise Exception(
"Programming error: mismatched sample names and counts")
counts.append(count)
observ_metadata.append({'taxonomy': tax})
otu_ids.append(str(otu_id))
table = Table(np.array(counts),
otu_ids,
sample_names,
observ_metadata, [{}] * len(sample_names),
table_id='GraftM Taxonomy Count Table')
try:
table.to_hdf5(biom_file_io, 'GraftM graft')
return True
except RuntimeError as e:
logging.warn(
"Error writing BIOM output, file not written. The specific error was: %s"
% e)
return False
def setUp(self):
rooted_nwk = io.StringIO("((A:0.1, B:0.2)C:0.3, D:0.4, E:0.5)root;")
self.tree = skbio.TreeNode.read(rooted_nwk)
self.metadata = Metadata(
pd.DataFrame(
data=np.array([['Bacteria', '1'], ['Archea', '1']],
dtype=object),
index=pd.Index(['A', 'D'], name='Feature ID'),
columns=['kingdom', 'keep'],
))
self.table = Table(data=np.array([[0, 1, 2], [2, 2, 2]]),
observation_ids=['A', 'D'],
sample_ids=['S1', 'S2', 'S3'])
self.filtered_tree = self.tree.copy().shear(['A', 'D'])
self.filtered_tree.prune()
def test_phylogenetic(self):
t = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
tree = skbio.TreeNode.read(
io.StringIO('((O1:0.25, O2:0.50):0.25, O3:0.75)root;'))
actual = beta_diversity('unweighted_unifrac', t, phylogeny=tree)
# expected computed with skbio.diversity.beta_diversity
expected = skbio.DistanceMatrix(
[[0.00, 0.25, 0.25], [0.25, 0.00, 0.00], [0.25, 0.00, 0.00]],
ids=['S1', 'S2', 'S3'])
self.assertEqual(actual.ids, expected.ids)
for id1 in actual.ids:
for id2 in actual.ids:
npt.assert_almost_equal(actual[id1, id2], expected[id1, id2])
def setUp(self):
THIS_DIR = os.path.dirname(os.path.abspath(__file__))
tablefp = Table({}, [], [])
self.emptyfeatures = tablefp
goodtable = os.path.join(THIS_DIR, 'data/features_formated.biom')
self.features = load_table(goodtable)
goodtable = os.path.join(THIS_DIR, 'data/features2_formated.biom')
self.features2 = load_table(goodtable)
self.goodcsi = qiime2.Artifact.load(
os.path.join(THIS_DIR, 'data/csiFolder.qza'))
goodcsi = self.goodcsi.view(CSIDirFmt)
self.collated = collate_fingerprint(goodcsi)
self.goodcsi2 = qiime2.Artifact.load(
os.path.join(THIS_DIR, 'data/csiFolder2.qza'))
goodcsi = self.goodcsi2.view(CSIDirFmt)
self.collated2 = collate_fingerprint(goodcsi)
def test_rarefy_to_files(self):
"""rarefy_to_files should write valid files
"""
maker = RarefactionMaker(self.otu_table_fp, 0, 1, 1, 1)
maker.rarefy_to_files(
self.rare_dir,
include_full=True,
include_lineages=False)
fname = os.path.join(self.rare_dir, "rarefaction_1_0.biom")
with biom_open(fname, 'U') as biom_file:
otu_table = Table.from_hdf5(biom_file)
self.assertItemsEqual(
otu_table.sample_ids,
self.otu_table.sample_ids[:2])
def test_filter_empty_features(self):
# no filtering
table = Table(np.array([[0, 1, 3], [1, 1, 2]]),
['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_samples(table, max_frequency=42,
filter_empty_features=False)
expected = Table(np.array([[0, 1, 3], [1, 1, 2]]),
['O1', 'O2'],
['S1', 'S2', 'S3'])
self.assertEqual(actual, expected)
# filter one
table = Table(np.array([[0, 1, 3], [1, 1, 2]]),
['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_samples(table, max_frequency=4,
filter_empty_features=False)
expected = Table(np.array([[0, 1], [1, 1]]),
['O1', 'O2'],
['S1', 'S2'])
self.assertEqual(actual, expected)
# filter two
table = Table(np.array([[0, 1, 3], [1, 1, 2]]),
['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_samples(table, max_frequency=1,
filter_empty_features=False)
expected = Table(np.array([[0], [1]]),
['O1', 'O2'],
['S1'])
self.assertEqual(actual, expected)
# filter all
table = Table(np.array([[0, 1, 3], [1, 1, 2]]),
['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_samples(table, max_frequency=0,
filter_empty_features=False)
expected = Table(np.array([[], []]), ['O1', 'O2'], [])
self.assertEqual(actual, expected)
def collapse_modules(table, modules):
"""collapse created modules in a biom table, members of multiple modules will be added to the smallest module"""
table = table.copy()
module_array = np.zeros((len(modules), table.shape[1]))
seen = set()
for module_, otus in modules.items():
module_number = int(module_.split('_')[-1])
seen = seen | set(otus)
# sum everything in the module
module_array[module_number] = np.sum([table.data(feature, axis="observation") for feature in otus], axis=0)
table.filter(seen, axis='observation', invert=True)
# make new table
new_table_matrix = np.concatenate((table.matrix_data.toarray(), module_array))
new_table_obs = list(table.ids(axis='observation')) + list(modules.keys())
return Table(new_table_matrix, new_table_obs, table.ids())
def calculate_correlations(
table: Table,
corr_method=spearmanr,
p_adjustment_method: str = 'fdr_bh') -> pd.DataFrame:
# TODO: multiprocess this
index = list()
data = list()
for (val_i, id_i, _), (val_j, id_j,
_) in table.iter_pairwise(axis='observation'):
r, p = corr_method(val_i, val_j)
index.append((id_i, id_j))
data.append((r, p))
correls = pd.DataFrame(data, index=index, columns=['r', 'p'])
correls.index = pd.MultiIndex.from_tuples(
correls.index) # Turn tuple index into actual multiindex
if p_adjustment_method is not None:
correls['p_adjusted'] = p_adjust(correls.p, method=p_adjustment_method)
return correls
def setUp(self):
self.qiime_config = load_qiime_config()
self.tmp_dir = self.qiime_config['temp_dir'] or '/tmp/'
self.otu_table_data = np.array([[2, 1, 0],
[0, 5, 0],
[0, 3, 0],
[1, 2, 0]])
self.sample_names = list('YXZ')
self.taxon_names = list('bacd')
self.otu_metadata = [{'domain': 'Archaea'},
{'domain': 'Bacteria'},
{'domain': 'Bacteria'},
{'domain': 'Bacteria'}]
self.otu_table = Table(self.otu_table_data,
self.taxon_names,
self.sample_names,
observation_metadata=[{}, {}, {}, {}],
sample_metadata=[{}, {}, {}])
self.otu_table_meta = Table(self.otu_table_data,
self.taxon_names, self.sample_names,
observation_metadata=self.otu_metadata)
fd, self.otu_table_fp = mkstemp(dir=self.tmp_dir,
prefix='test_rarefaction',
suffix='.biom')
close(fd)
fd, self.otu_table_meta_fp = mkstemp(dir=self.tmp_dir,
prefix='test_rarefaction',
suffix='.biom')
close(fd)
self.rare_dir = mkdtemp(dir=self.tmp_dir,
prefix='test_rarefaction_dir', suffix='')
write_biom_table(self.otu_table, self.otu_table_fp)
write_biom_table(self.otu_table_meta, self.otu_table_meta_fp)
self._paths_to_clean_up = [self.otu_table_fp, self.otu_table_meta_fp]
self._dirs_to_clean_up = [self.rare_dir]
def test_make_otu_table_taxonomy(self):
"""make_otu_table should work with taxonomy"""
otu_map_lines = """0 ABC_0 DEF_1
1 ABC_1
x GHI_2 GHI_3 GHI_77
z DEF_3 XYZ_1""".split('\n')
taxonomy = {'0': ['Bacteria', 'Firmicutes'],
'x': ['Bacteria', 'Bacteroidetes']}
obs = make_otu_table(otu_map_lines, taxonomy)
data = [[1, 1, 0, 0], [1, 0, 0, 0], [0, 0, 3, 0], [0, 1, 0, 1]]
obs_md = [{'taxonomy': ['Bacteria', 'Firmicutes']},
{'taxonomy': ['None']},
{'taxonomy': ['Bacteria', 'Bacteroidetes']},
{'taxonomy': ['None']}]
exp = Table(data, ['0', '1', 'x', 'z'], ['ABC', 'DEF', 'GHI', 'XYZ'],
observation_metadata=obs_md, input_is_dense=True)
self.assertEqual(obs, exp)
def test_parallel_beta(self):
t = Table(np.array([[0, 1, 3], [1, 1, 2]]), ['O1', 'O2'],
['S1', 'S2', 'S3'])
parallel = beta(table=t, metric='braycurtis', n_jobs=-1)
single_thread = beta(table=t, metric='braycurtis', n_jobs=1)
# expected computed with scipy.spatial.distance.braycurtis
expected = skbio.DistanceMatrix([[0.0000000, 0.3333333, 0.6666667],
[0.3333333, 0.0000000, 0.4285714],
[0.6666667, 0.4285714, 0.0000000]],
ids=['S1', 'S2', 'S3'])
self.assertEqual(parallel.ids, expected.ids)
self.assertEqual(single_thread.ids, expected.ids)
for id1 in parallel.ids:
for id2 in parallel.ids:
npt.assert_almost_equal(parallel[id1, id2], expected[id1, id2])
for id1 in single_thread.ids:
for id2 in single_thread.ids:
npt.assert_almost_equal(single_thread[id1, id2], expected[id1,
id2])
def test_write_biom_table(self):
"""Test functionality of write_biom_table().
"""
table_exp = Table(np.array([[1., 1., 1., 0., 0.],
[1., 0., 0., 0., 0.],
[0., 0., 1., 0., 1.],
[0., 0., 0., 1., 0.],
[0., 0., 0., 1., 0.],
[0., 0., 1., 0., 0.]]),
["k__Bacteria;p__Actinobacteria;c__Actinobacteria;o__Actinomycetales;f__Propionibacteriaceae;g__Propionibacterium",
"k__Bacteria;p__Firmicutes;c__Bacilli;o__Bacillales;f__Staphylococcaceae;g__Staphylococcus",
"k__Bacteria;p__Proteobacteria;c__Gammaproteobacteria;o__Enterobacteriales;f__Enterobacteriaceae;g__Escherichia",
"k__Bacteria;p__Actinobacteria;c__Actinobacteria;o__Actinomycetales;f__Actinomycetaceae;g__Mobiluncus",
"k__Bacteria;p__Proteobacteria;c__Gammaproteobacteria;o__Xanthomonadales;f__Xanthomonadaceae;g__Stenotrophomonas",
"k__Bacteria;p__Actinobacteria;c__Actinobacteria;o__Actinomycetales;f__Corynebacteriaceae;g__Corynebacterium"],
["s1", "s2", "s3", "s4", "s5"])
self.biom_output_fp = join(self.working_dir, "test_output_biom")
write_biom_table(table_exp, self.biom_output_fp)
table_obs = load_table(self.biom_output_fp)
self.assertEqual(table_obs, table_exp)
def test_max_frequency(self):
# no filtering
table = Table(np.array([[0, 1, 3], [1, 1, 2]]),
['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_samples(table, max_frequency=42)
expected = Table(np.array([[0, 1, 3], [1, 1, 2]]),
['O1', 'O2'],
['S1', 'S2', 'S3'])
self.assertEqual(actual, expected)
# filter one
table = Table(np.array([[0, 1, 3], [1, 1, 2]]),
['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_samples(table, max_frequency=4)
expected = Table(np.array([[0, 1], [1, 1]]),
['O1', 'O2'],
['S1', 'S2'])
self.assertEqual(actual, expected)
# filter two
table = Table(np.array([[0, 1, 3], [1, 1, 2]]),
['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_samples(table, max_frequency=1)
expected = Table(np.array([[1]]),
['O2'],
['S1'])
self.assertEqual(actual, expected)
# filter all
table = Table(np.array([[0, 1, 3], [1, 1, 2]]),
['O1', 'O2'],
['S1', 'S2', 'S3'])
actual = filter_samples(table, max_frequency=0)
expected = Table(np.array([]), [], [])
self.assertEqual(actual, expected)
def collapse_modules(table, modules, prefix="module"):
"""collapse created modules in a biom table, members of multiple modules will be added to the smallest module"""
table = table.copy()
module_array = np.zeros((len(modules), table.shape[1]))
seen = set()
for i, module_ in enumerate(modules):
seen = seen | module_
# sum everything in the module
module_array[i] = np.sum(
[table.data(feature, axis="observation") for feature in module_],
axis=0)
table.filter(seen, axis='observation', invert=True)
# make new table
new_table_matrix = np.concatenate(
(table.matrix_data.toarray(), module_array))
new_table_obs = list(table.ids(axis='observation')) + [
'_'.join([prefix, str(i)]) for i in range(len(modules))
]
return Table(new_table_matrix, new_table_obs, table.ids())
def biom_table2():
arr = np.array([[250, 0, 100, 446, 75], [0, 0, 1, 1, 2], [2, 2, 2, 2, 2],
[100, 100, 500, 1, 1000], [500, 5, 0, 50, 100]])
obs_ids = ["otu_%s" % i for i in range(5)]
samp_ids = ["samp_%s" % i for i in range(5)]
obs_meta = [{
'taxonomy':
'k__Bacteria; p__Firmicutes; c__Bacilli; o__Bacillales; f__Staphylococcaceae; g__Staphylococcus; s__'
}, {
'taxonomy':
'k__Bacteria; p__Firmicutes; c__Bacilli; o__Bacillales; f__Paenibacillaceae; g__Paenibacillus; s__'
}, {
'taxonomy':
'k__Bacteria; p__Proteobacteria; c__Betaproteobacteria; o__Methylophilales; f__Methylophilaceae; g__; s__'
}, {
'taxonomy':
'k__Bacteria; p__Firmicutes; c__Clostridia; o__Clostridiales; f__Lachnospiraceae; g__[Ruminococcus]; s__'
}, {
'taxonomy':
'k__Bacteria; p__Actinobacteria; c__Actinobacteria; o__Actinomycetales; f__Microbacteriaceae; g__; s__'
}]
return Table(arr, obs_ids, samp_ids, observation_metadata=obs_meta)
def calculate_correlations(table: Table, corr_method=spearmanr, p_adjust_method: str = 'fdr_bh', nprocs=1) -> \
pd.DataFrame:
if nprocs > multiprocessing.cpu_count():
warnings.warn(
"nprocs greater than CPU count, using all avaliable CPUs")
nprocs = multiprocessing.cpu_count()
pool = multiprocessing.Pool(nprocs)
cor = partial(calculate_correlation, corr_method=corr_method)
results = pool.map(
cor,
pairwise_iter_wo_metadata(table.iter_pairwise(axis='observation')))
index = [i[0] for i in results]
data = [i[1] for i in results]
pool.close()
pool.join()
correls = pd.DataFrame(data, index=index, columns=['r', 'p'])
# Turn tuple index into actual multiindex, now guaranteeing that correls index is sorted
correls.index = pd.MultiIndex.from_tuples(
[sorted(i) for i in correls.index])
if p_adjust_method is not None:
correls['p_adjusted'] = p_adjust(correls.p, method=p_adjust_method)
return correls
def generate_biom_table(seqs_fp, uc_fp, delim='_'):
"""Generate BIOM table and representative FASTA set
Parameters
----------
seqs_fp: string
file path to deblurred sequences
uc_fp: string
file path to dereplicated sequences map (.uc format)
delim: string, optional
delimiter for splitting sample and sequence IDs in sequence label
default: '_'
Returns
-------
deblur_clusters: dictionary
dictionary of clusters including dereplicated sequence labels
Table: biom.table
an instance of a BIOM table
"""
# parse clusters in dereplicated sequences map (.uc format)
with open(uc_fp, 'U') as uc_f:
derep_clusters, failures, seeds = clusters_from_uc_file(uc_f)
# parse clusters in deblur file, set observation ID to be the sequence
deblur_clusters = parse_deblur_output(seqs_fp, derep_clusters)
# create sparse dictionary of observation and sample ID counts
data, otu_ids, sample_ids = generate_biom_data(deblur_clusters, delim)
# build BIOM table
return deblur_clusters, Table(data,
otu_ids,
sample_ids,
observation_metadata=None,
sample_metadata=None,
table_id=None,
generated_by="deblur",
create_date=datetime.now().isoformat())
def main():
option_parser, opts, args = parse_command_line_parameters(**script_info)
lower_percentage = opts.lower_percentage
upper_percentage = opts.upper_percentage
otu_table_fp = opts.otu_table_fp
otu_table = load_table(otu_table_fp)
delimiter = opts.delimiter
mapping_fp = opts.mapping
md_as_string = opts.md_as_string
md_identifier = opts.md_identifier
levels = opts.level.split(',')
suppress_classic_table_output = opts.suppress_classic_table_output
suppress_biom_table_output = opts.suppress_biom_table_output
if upper_percentage is not None and lower_percentage is not None:
raise ValueError(
"upper_percentage and lower_percentage are mutually exclusive")
if upper_percentage is not None and lower_percentage is not None and \
mapping:
raise ValueError("upper_percentage and lower_percentage can not be "
"using with mapping file")
if upper_percentage is not None and \
(upper_percentage < 0 or upper_percentage > 1.0):
raise ValueError('max_otu_percentage should be between 0.0 and 1.0')
if lower_percentage is not None and \
(lower_percentage < 0 or lower_percentage > 1.0):
raise ValueError('lower_percentage should be between 0.0 and 1.0')
if mapping_fp:
mapping_file = open(mapping_fp, 'U')
mapping, header, comments = parse_mapping_file(mapping_file)
# use the input Mapping file for producing the output filenames
map_dir_path, map_fname = split(mapping_fp)
map_basename, map_fname_ext = splitext(map_fname)
else:
if suppress_classic_table_output and suppress_biom_table_output:
option_parser.error("Both classic and BIOM output formats were "
"suppressed.")
if not opts.absolute_abundance:
otu_table = otu_table.norm(axis='sample', inplace=False)
# introduced output directory to will allow for multiple outputs
if opts.output_dir:
create_dir(opts.output_dir, False)
output_dir_path = opts.output_dir
else:
output_dir_path = './'
# use the input OTU table to produce the output filenames
dir_path, fname = split(otu_table_fp)
basename, fname_ext = splitext(fname)
# Iterate over the levels and generate a summarized taxonomy for each
for level in levels:
if mapping_fp:
# define output filename
output_fname = join(output_dir_path,
map_basename + '_L%s.txt' % (level))
summary, tax_order = add_summary_mapping(otu_table,
mapping,
int(level),
md_as_string,
md_identifier)
write_add_taxa_summary_mapping(summary, tax_order, mapping,
header, output_fname, delimiter)
else:
# define the output filename. The extension will be added to the
# end depending on the output format
output_fname = join(output_dir_path, basename + '_L%s' % level)
summary, header = make_summary(otu_table,
int(level),
upper_percentage,
lower_percentage,
md_as_string,
md_identifier)
sample_ids = header[1:]
observation_ids = []
data = []
for row in summary:
# Join taxonomic levels to create an observation ID.
observation_ids.append(delimiter.join(row[0]))
data.append(row[1:])
table = Table(np.asarray(data), observation_ids, sample_ids)
if opts.transposed_output:
table = table.transpose()
if not suppress_classic_table_output:
with open(output_fname + '.txt', 'w') as outfile:
outfile.write(table.to_tsv())
if not suppress_biom_table_output:
write_biom_table(table, output_fname + '.biom')
def parse_biom_table(fp, ids=None, axis='sample', input_is_dense=False):
r"""Parses the biom table stored in the filepath `fp`
Parameters
----------
fp : file like
File alike object storing the BIOM table
ids : iterable
The sample/observation ids of the samples/observations that we need
to retrieve from the biom table
axis : {'sample', 'observation'}, optional
The axis to subset on
input_is_dense : boolean
Indicates if the BIOM table is dense or sparse. Valid only for JSON
tables.
Returns
-------
Table
The BIOM table stored at fp
Raises
------
ValueError
If `samples` and `observations` are provided.
Notes
-----
Subsetting from the BIOM table is only supported in one axis
Examples
--------
Parse a hdf5 biom table
>>> from h5py import File # doctest: +SKIP
>>> from biom.parse import parse_biom_table
>>> f = File('rich_sparse_otu_table_hdf5.biom') # doctest: +SKIP
>>> t = parse_biom_table(f) # doctest: +SKIP
Parse a hdf5 biom table subsetting observations
>>> from h5py import File # doctest: +SKIP
>>> from biom.parse import parse_biom_table
>>> f = File('rich_sparse_otu_table_hdf5.biom') # doctest: +SKIP
>>> t = parse_biom_table(f, ids=["GG_OTU_1"],
... axis='observation') # doctest: +SKIP
"""
if axis not in ['observation', 'sample']:
UnknownAxisError(axis)
try:
return Table.from_hdf5(fp, ids=ids, axis=axis)
except ValueError:
pass
except RuntimeError:
pass
if hasattr(fp, 'read'):
old_pos = fp.tell()
# Read in characters until first non-whitespace
# If it is a {, then this is (most likely) JSON
c = fp.read(1)
while c.isspace():
c = fp.read(1)
if c == '{':
fp.seek(old_pos)
t = Table.from_json(json.load(fp, object_pairs_hook=OrderedDict),
input_is_dense=input_is_dense)
else:
fp.seek(old_pos)
t = Table.from_tsv(fp, None, None, lambda x: x)
elif isinstance(fp, list):
try:
t = Table.from_json(json.loads(''.join(fp),
object_pairs_hook=OrderedDict),
input_is_dense=input_is_dense)
except ValueError:
t = Table.from_tsv(fp, None, None, lambda x: x)
else:
t = Table.from_json(json.loads(fp, object_pairs_hook=OrderedDict),
input_is_dense=input_is_dense)
def subset_ids(data, id_, md):
return id_ in ids
def gt_zero(vals, id_, md):
return np.any(vals)
if ids is not None:
t.filter(subset_ids, axis=axis)
axis = 'observation' if axis == 'sample' else 'sample'
t.filter(gt_zero, axis=axis)
return t
class TopLevelTests(TestCase):
"""Tests of top-level functions"""
def setUp(self):
self.otu_table_vals = array([[1, 0, 2, 4],
[1, 2, 0, 1],
[0, 1, 1, 0],
[1, 2, 1, 0]])
self.otu_table = Table(self.otu_table_vals,
['0', '1', '2', '3'],
['s1', 's2', 's3', 's4'],
[{"taxonomy": ["Root", "Bacteria", "Actinobacteria", "Actinobacteria", "Coriobacteridae", "Coriobacteriales", "Coriobacterineae", "Coriobacteriaceae"]},
{"taxonomy": ["Root",
"Bacteria",
"Firmicutes",
"\"Clostridia\""]},
{"taxonomy": ["Root",
"Bacteria",
"Firmicutes",
"\"Clostridia\""]},
{"taxonomy": ["Root", "Bacteria"]}],
None,)
self.mapping = """#SampleID\tBarcodeSequence\tTreatment\tDescription
#Test mapping file
s1\tAAAA\tControl\tControl mouse, I.D. 354
s2\tGGGG\tControl\tControl mouse, I.D. 355
s3\tCCCC\tExp\tDisease mouse, I.D. 356
s4\tTTTT\tExp\tDisease mouse, I.D. 357""".split('\n')
def test_sum_counts_by_consensus(self):
"""should sum otu counts by consensus"""
#otu_table = parse_otu_table(self.otu_table)
#otu_table = parse_biom_table(self.otu_table)
obs_result, obs_mapping = sum_counts_by_consensus(self.otu_table, 3)
exp_result = {(
'Root', 'Bacteria', 'Actinobacteria'): array([1, 0, 2, 4]),
('Root', 'Bacteria', 'Firmicutes'): array([1, 3, 1, 1]),
('Root', 'Bacteria', 'Other'): array([1, 2, 1, 0])}
exp_mapping = {'s1': 0, 's2': 1, 's3': 2, 's4': 3}
self.assertItemsEqual(obs_result, exp_result)
self.assertEqual(obs_mapping, exp_mapping)
obs_result, obs_mapping = sum_counts_by_consensus(self.otu_table, 2)
exp_result = {('Root', 'Bacteria'): array([3, 5, 4, 5])}
exp_mapping = {'s1': 0, 's2': 1, 's3': 2, 's4': 3}
self.assertItemsEqual(obs_result, exp_result)
self.assertEqual(obs_mapping, exp_mapping)
obs_result, obs_mapping = sum_counts_by_consensus(self.otu_table, 4)
exp_result = {('Root', 'Bacteria', 'Actinobacteria', 'Actinobacteria'):
array([1, 0, 2, 4]),
('Root', 'Bacteria', 'Firmicutes', '"Clostridia"'):
array([1, 3, 1, 1]),
('Root', 'Bacteria', 'Other', 'Other'): array([1, 2, 1, 0])}
exp_mapping = {'s1': 0, 's2': 1, 's3': 2, 's4': 3}
self.assertItemsEqual(obs_result, exp_result)
self.assertEqual(obs_mapping, exp_mapping)
def test_make_new_summary_file(self):
"""make_new_summary_file works
"""
lower_percentage, upper_percentage = None, None
#otu_table = parse_otu_table(self.otu_table, int)
#otu_table = parse_biom_table(self.otu_table)
summary, header = make_summary(
self.otu_table, 3, upper_percentage, lower_percentage)
self.assertEqual(header, ['Taxon', 's1', 's2', 's3', 's4'])
self.assertEqual(
summary, [[('Root', 'Bacteria', 'Actinobacteria'), 1, 0, 2, 4],
[('Root', 'Bacteria', 'Firmicutes'),
1, 3, 1, 1],
[('Root', 'Bacteria', 'Other'), 1, 2, 1, 0]])
# test that works with relative abundances
#otu_table = parse_otu_table(self.otu_table, float)
#otu_table = parse_biom_table(self.otu_table, float)
#otu_table = convert_otu_table_relative(otu_table)
otu_table = self.otu_table.norm(axis='sample', inplace=False)
summary, header = make_summary(
otu_table, 3, upper_percentage, lower_percentage)
self.assertEqual(header, ['Taxon', 's1', 's2', 's3', 's4'])
self.assertEqual(summary[0][0], ('Root', 'Bacteria', 'Actinobacteria'))
assert_almost_equal(summary[0][1:], [1.0 / 3, 0.0, 0.5, 0.8])
self.assertEqual(summary[1][0], ('Root', 'Bacteria', 'Firmicutes'))
assert_almost_equal(summary[1][1:], [1.0 / 3, 0.6, 0.25, 0.2])
self.assertEqual(summary[2][0], ('Root', 'Bacteria', 'Other'))
assert_almost_equal(summary[2][1:], [1.0 / 3, 0.4, 0.25, 0.0])
##
# testing lower triming
lower_percentage, upper_percentage = 0.3, None
summary, header = make_summary(
otu_table, 3, upper_percentage, lower_percentage)
self.assertEqual(summary[0][0], ('Root', 'Bacteria', 'Other'))
assert_almost_equal(summary[0][1:], [1.0 / 3, 0.4, 0.25, 0.0])
##
# testing upper triming
lower_percentage, upper_percentage = None, 0.4
summary, header = make_summary(
otu_table, 3, upper_percentage, lower_percentage)
self.assertEqual(summary[0][0], ('Root', 'Bacteria', 'Actinobacteria'))
assert_almost_equal(summary[0][1:], [1.0 / 3, 0.0, 0.5, 0.8])
def test_add_summary_category_mapping(self):
"""make_new_summary_file works
"""
#otu_table = parse_otu_table(self.otu_table, int)
#otu_table = parse_biom_table(self.otu_table)
mapping, header, comments = parse_mapping_file(self.mapping)
summary, taxon_order = add_summary_mapping(self.otu_table, mapping, 3)
self.assertEqual(taxon_order, [('Root', 'Bacteria', 'Actinobacteria'),
('Root', 'Bacteria', 'Firmicutes'),
('Root', 'Bacteria', 'Other')])
self.assertEqual(summary, {'s1': [1, 1, 1],
's2': [0, 3, 2],
's3': [2, 1, 1],
's4': [4, 1, 0]})
# print "index: %i" %index
ind_taxonomy.append('%s%s' %(syn[levels[index]], taxon[0]['ScientificName']))
# print ind_taxonomy
Taxonomy[taxon[0]['ScientificName']]['taxonomy'] = ind_taxonomy
# print "Taxonomy: %s" %Taxonomy
for taxon in observ_ids:
# print taxon
# print Taxonomy[taxon]
observation_metadata.append(Taxonomy[taxon])
#print "observation metadata:\n%s" %observation_metadata
#print len(observation_metadata)
table = Table(data, observ_ids, sample_id, observation_metadata, sample_metadata, table_id='Example Table')
print table
out=open(args.prefix+".biom","w")
table.to_json('pplacer converted by jplace_to_biom.py v.'+VERSION, direct_io=out)
out.close()
out=open(args.prefix+".tsv","w")
out.write(table.to_tsv(header_key='taxonomy', header_value='taxomomy')) #to_json('generaged by test', direct_io=out)
out.close()
print "\n##### DONE! #####\n"
def gibbs(table_fp, mapping_fp, output_dir, loo, jobs, alpha1, alpha2, beta,
source_rarefaction_depth, sink_rarefaction_depth,
restarts, draws_per_restart, burnin, delay, cluster_start_delay,
source_sink_column, source_column_value, sink_column_value,
source_category_column):
'''Gibb's sampler for Bayesian estimation of microbial sample sources.
For details, see the project README file.
'''
# Create results directory. Click has already checked if it exists, and
# failed if so.
os.mkdir(output_dir)
# Load the mapping file and biom table and remove samples which are not
# shared.
o = open(mapping_fp, 'U')
sample_metadata_lines = o.readlines()
o.close()
sample_metadata, biom_table = \
_cli_sync_biom_and_sample_metadata(
parse_mapping_file(sample_metadata_lines),
load_table(table_fp))
# If biom table has fractional counts, it can produce problems in indexing
# later on.
biom_table.transform(lambda data, id, metadata: np.ceil(data))
# If biom table has sample metadata, there will be pickling errors when
# submitting multiple jobs. We remove the metadata by making a copy of the
# table without metadata.
biom_table = Table(biom_table._data.toarray(),
biom_table.ids(axis='observation'),
biom_table.ids(axis='sample'))
# Parse the mapping file and options to get the samples requested for
# sources and sinks.
source_samples, sink_samples = sinks_and_sources(
sample_metadata, column_header=source_sink_column,
source_value=source_column_value, sink_value=sink_column_value)
# If we have no source samples neither normal operation or loo will work.
# Will also likely get strange errors.
if len(source_samples) == 0:
raise ValueError('Mapping file or biom table passed contain no '
'`source` samples.')
# Prepare the 'sources' matrix by collapsing the `source_samples` by their
# metadata values.
sources_envs, sources_data = collapse_sources(source_samples,
sample_metadata,
source_category_column,
biom_table, sort=True)
# Rarefiy data if requested.
sources_data, biom_table = \
subsample_sources_sinks(sources_data, sink_samples, biom_table,
source_rarefaction_depth,
sink_rarefaction_depth)
# Build function that require only a single parameter -- sample -- to
# enable parallel processing if requested.
if loo:
f = partial(_cli_loo_runner, source_category=source_category_column,
alpha1=alpha1, alpha2=alpha2, beta=beta,
restarts=restarts, draws_per_restart=draws_per_restart,
burnin=burnin, delay=delay,
sample_metadata=sample_metadata,
sources_data=sources_data, sources_envs=sources_envs,
biom_table=biom_table, output_dir=output_dir)
sample_iter = source_samples
else:
f = partial(_cli_sink_source_prediction_runner, alpha1=alpha1,
alpha2=alpha2, beta=beta, restarts=restarts,
draws_per_restart=draws_per_restart, burnin=burnin,
delay=delay, sources_data=sources_data,
biom_table=biom_table, output_dir=output_dir)
sample_iter = sink_samples
if jobs > 1:
# Launch the ipcluster and wait for it to come up.
subprocess.Popen('ipcluster start -n %s --quiet' % jobs, shell=True)
time.sleep(cluster_start_delay)
c = Client()
c[:].map(f, sample_iter, block=True)
# Shut the cluster down. Answer taken from SO:
# http://stackoverflow.com/questions/30930157/stopping-ipcluster-engines-ipython-parallel
c.shutdown(hub=True)
else:
for sample in sample_iter:
f(sample)
# Format results for output.
samples = []
samples_data = []
for sample_fp in glob.glob(os.path.join(output_dir, '*')):
samples.append(sample_fp.strip().split('/')[-1].split('.txt')[0])
samples_data.append(np.loadtxt(sample_fp, delimiter='\t'))
mp, mps = _cli_collate_results(samples, samples_data, sources_envs)
o = open(os.path.join(output_dir, 'mixing_proportions.txt'), 'w')
o.writelines(mp)
o.close()
o = open(os.path.join(output_dir, 'mixing_proportions_stds.txt'), 'w')
o.writelines(mps)
o.close()
class TopLevelTests(TestCase):
"""Tests of top-level functions"""
def setUp(self):
"""define some top-level data"""
self.otu_table_values = array([[0, 0, 9, 5, 3, 1], [1, 5, 4, 0, 3, 2], [2, 3, 1, 1, 2, 5]])
{
(0, 2): 9.0,
(0, 3): 5.0,
(0, 4): 3.0,
(0, 5): 1.0,
(1, 0): 1.0,
(1, 1): 5.0,
(1, 2): 4.0,
(1, 4): 3.0,
(1, 5): 2.0,
(2, 0): 2.0,
(2, 1): 3.0,
(2, 2): 1.0,
(2, 3): 1.0,
(2, 4): 2.0,
(2, 5): 5.0,
}
self.otu_table = Table(
self.otu_table_values,
["OTU1", "OTU2", "OTU3"],
["Sample1", "Sample2", "Sample3", "Sample4", "Sample5", "Sample6"],
[{"taxonomy": ["Bacteria"]}, {"taxonomy": ["Archaea"]}, {"taxonomy": ["Streptococcus"]}],
[None, None, None, None, None, None],
)
self.otu_table_f = Table(
self.otu_table_values,
["OTU1", "OTU2", "OTU3"],
["Sample1", "Sample2", "Sample3", "Sample4", "Sample5", "Sample6"],
[
{"taxonomy": ["1A", "1B", "1C", "Bacteria"]},
{"taxonomy": ["2A", "2B", "2C", "Archaea"]},
{"taxonomy": ["3A", "3B", "3C", "Streptococcus"]},
],
[None, None, None, None, None, None],
)
self.full_lineages = [
["1A", "1B", "1C", "Bacteria"],
["2A", "2B", "2C", "Archaea"],
["3A", "3B", "3C", "Streptococcus"],
]
self.metadata = [
[
["Sample1", "NA", "A"],
["Sample2", "NA", "B"],
["Sample3", "NA", "A"],
["Sample4", "NA", "B"],
["Sample5", "NA", "A"],
["Sample6", "NA", "B"],
],
["SampleID", "CAT1", "CAT2"],
[],
]
self.tree_text = ["('OTU3',('OTU1','OTU2'))"]
fh, self.tmp_heatmap_fpath = mkstemp(prefix="test_heatmap_", suffix=".pdf")
close(fh)
def test_extract_metadata_column(self):
"""Extracts correct column from mapping file"""
obs = extract_metadata_column(self.otu_table.sample_ids, self.metadata, category="CAT2")
exp = ["A", "B", "A", "B", "A", "B"]
self.assertEqual(obs, exp)
def test_get_order_from_categories(self):
"""Sample indices should be clustered within each category"""
category_labels = ["A", "B", "A", "B", "A", "B"]
obs = get_order_from_categories(self.otu_table, category_labels)
group_string = "".join([category_labels[i] for i in obs])
self.assertTrue("AAABBB" == group_string or group_string == "BBBAAA")
def test_get_order_from_tree(self):
obs = get_order_from_tree(self.otu_table.observation_ids, self.tree_text)
exp = [2, 0, 1]
assert_almost_equal(obs, exp)
def test_make_otu_labels(self):
lineages = []
for val, id, meta in self.otu_table.iter(axis="observation"):
lineages.append([v for v in meta["taxonomy"]])
obs = make_otu_labels(self.otu_table.observation_ids, lineages, n_levels=1)
exp = ["Bacteria (OTU1)", "Archaea (OTU2)", "Streptococcus (OTU3)"]
self.assertEqual(obs, exp)
full_lineages = []
for val, id, meta in self.otu_table_f.iter(axis="observation"):
full_lineages.append([v for v in meta["taxonomy"]])
obs = make_otu_labels(self.otu_table_f.observation_ids, full_lineages, n_levels=3)
exp = ["1B;1C;Bacteria (OTU1)", "2B;2C;Archaea (OTU2)", "3B;3C;Streptococcus (OTU3)"]
self.assertEqual(obs, exp)
def test_names_to_indices(self):
new_order = ["Sample4", "Sample2", "Sample3", "Sample6", "Sample5", "Sample1"]
obs = names_to_indices(self.otu_table.sample_ids, new_order)
exp = [3, 1, 2, 5, 4, 0]
assert_almost_equal(obs, exp)
def test_get_log_transform(self):
obs = get_log_transform(self.otu_table)
data = [val for val in self.otu_table.iter_data(axis="observation")]
xform = asarray(data, dtype=float64)
for (i, val) in enumerate(obs.iter_data(axis="observation")):
non_zeros = argwhere(xform[i] != 0)
xform[i, non_zeros] = log10(xform[i, non_zeros])
assert_almost_equal(val, xform[i])
def test_get_clusters(self):
data = asarray([val for val in self.otu_table.iter_data(axis="observation")])
obs = get_clusters(data, axis="row")
self.assertTrue([0, 1, 2] == obs or obs == [1, 2, 0])
obs = get_clusters(data, axis="column")
exp = [2, 3, 1, 4, 0, 5]
self.assertEqual(obs, exp)
def test_plot_heatmap(self):
plot_heatmap(
self.otu_table, self.otu_table.observation_ids, self.otu_table.sample_ids, filename=self.tmp_heatmap_fpath
)
self.assertEqual(exists(self.tmp_heatmap_fpath), True)
remove_files(set([self.tmp_heatmap_fpath]))
def parse_biom_table(fp, ids=None, axis='sample', input_is_dense=False):
r"""Parses the biom table stored in the filepath `fp`
Parameters
----------
fp : file like
File alike object storing the BIOM table
ids : iterable
The sample/observation ids of the samples/observations that we need
to retrieve from the biom table
axis : {'sample', 'observation'}, optional
The axis to subset on
input_is_dense : boolean
Indicates if the BIOM table is dense or sparse. Valid only for JSON
tables.
Returns
-------
Table
The BIOM table stored at fp
Raises
------
ValueError
If `samples` and `observations` are provided.
Notes
-----
Subsetting from the BIOM table is only supported in one axis
Examples
--------
Parse a hdf5 biom table
>>> from h5py import File # doctest: +SKIP
>>> from biom.parse import parse_biom_table
>>> f = File('rich_sparse_otu_table_hdf5.biom') # doctest: +SKIP
>>> t = parse_biom_table(f) # doctest: +SKIP
Parse a hdf5 biom table subsetting observations
>>> from h5py import File # doctest: +SKIP
>>> from biom.parse import parse_biom_table
>>> f = File('rich_sparse_otu_table_hdf5.biom') # doctest: +SKIP
>>> t = parse_biom_table(f, ids=["GG_OTU_1"],
... axis='observation') # doctest: +SKIP
"""
if axis not in ['observation', 'sample']:
UnknownAxisError(axis)
try:
return Table.from_hdf5(fp, ids=ids, axis=axis)
except:
pass
if hasattr(fp, 'read'):
old_pos = fp.tell()
try:
t = Table.from_json(json.load(fp), input_is_dense=input_is_dense)
except ValueError:
fp.seek(old_pos)
t = Table.from_tsv(fp, None, None, lambda x: x)
elif isinstance(fp, list):
try:
t = Table.from_json(json.loads(''.join(fp)),
input_is_dense=input_is_dense)
except ValueError:
t = Table.from_tsv(fp, None, None, lambda x: x)
else:
t = Table.from_json(json.loads(fp), input_is_dense=input_is_dense)
if ids is not None:
f = lambda data, id_, md: id_ in ids
t.filter(f, axis=axis)
axis = 'observation' if axis == 'sample' else 'sample'
f = lambda vals, id_, md: np.any(vals)
t.filter(f, axis=axis)
return t
class FunctionTests(TestCase):
def setUp(self):
self.tmp_dir = get_qiime_temp_dir()
self.otu_table_data = np.array([[2, 1, 0],
[0, 5, 0],
[0, 3, 0],
[1, 2, 0]])
self.sample_names = list('YXZ')
self.taxon_names = list('bacd')
self.otu_metadata = [{'domain': 'Archaea'},
{'domain': 'Bacteria'},
{'domain': 'Bacteria'},
{'domain': 'Bacteria'}]
self.otu_table = Table(self.otu_table_data,
self.taxon_names,
self.sample_names)
self.otu_table_meta = Table(self.otu_table_data,
self.taxon_names, self.sample_names,
observation_metadata=self.otu_metadata)
fd, self.otu_table_fp = mkstemp(dir=self.tmp_dir,
prefix='test_rarefaction',
suffix='.biom')
close(fd)
fd, self.otu_table_meta_fp = mkstemp(dir=self.tmp_dir,
prefix='test_rarefaction',
suffix='.biom')
close(fd)
self.rare_dir = mkdtemp(dir=self.tmp_dir,
prefix='test_rarefaction_dir', suffix='')
write_biom_table(self.otu_table, self.otu_table_fp)
write_biom_table(self.otu_table_meta, self.otu_table_meta_fp)
self._paths_to_clean_up = [self.otu_table_fp, self.otu_table_meta_fp]
self._dirs_to_clean_up = [self.rare_dir]
def tearDown(self):
""" cleanup temporary files """
map(remove, self._paths_to_clean_up)
for d in self._dirs_to_clean_up:
if os.path.exists(d):
rmtree(d)
def test_rarefy_to_list(self):
"""rarefy_to_list should rarefy correctly, same names
"""
maker = RarefactionMaker(self.otu_table_fp, 0, 1, 1, 1)
res = maker.rarefy_to_list(include_full=True)
self.assertItemsEqual(res[-1][2].ids(), self.otu_table.ids())
self.assertItemsEqual(
res[-1][2].ids(axis='observation'),
self.otu_table.ids(axis='observation'))
self.assertEqual(res[-1][2], self.otu_table)
sample_value_sum = []
for val in res[1][2].iter_data(axis='sample'):
sample_value_sum.append(val.sum())
npt.assert_almost_equal(sample_value_sum, [1.0, 1.0])
def test_rarefy_to_files(self):
"""rarefy_to_files should write valid files
"""
maker = RarefactionMaker(self.otu_table_fp, 1, 2, 1, 1)
maker.rarefy_to_files(
self.rare_dir,
include_full=True,
include_lineages=False)
fname = os.path.join(self.rare_dir, "rarefaction_1_0.biom")
otu_table = load_table(fname)
self.assertItemsEqual(
otu_table.ids(),
self.otu_table.ids()[:2])
# third sample had 0 seqs, so it's gone
def test_rarefy_to_files2(self):
"""rarefy_to_files should write valid files with some metadata on otus
"""
maker = RarefactionMaker(self.otu_table_meta_fp, 1, 2, 1, 1)
maker.rarefy_to_files(
self.rare_dir,
include_full=True,
include_lineages=False)
fname = os.path.join(self.rare_dir, "rarefaction_1_0.biom")
otu_table = load_table(fname)
self.assertItemsEqual(
otu_table.ids(),
self.otu_table.ids()[:2])
# third sample had 0 seqs, so it's gone
def test_get_empty_rare(self):
"""get_rare_data should be empty when depth > # seqs in any sample"""
self.assertRaises(TableException, get_rare_data, self.otu_table,
50, include_small_samples=False)
def test_get_overfull_rare(self):
"""get_rare_data should be identical to given in this case
here, rare depth > any sample, and include_small... = True"""
rare_otu_table = get_rare_data(self.otu_table,
50, include_small_samples=True)
self.assertEqual(len(rare_otu_table.ids()), 3)
# 4 observations times 3 samples = size 12 before
self.assertEqual(len(rare_otu_table.ids(axis='observation')), 4)
for sam in self.otu_table.ids():
for otu in self.otu_table.ids(axis='observation'):
rare_val = rare_otu_table.get_value_by_ids(otu, sam)
self.assertEqual(rare_otu_table.get_value_by_ids(otu, sam),
self.otu_table.get_value_by_ids(otu, sam))
def test_get_11depth_rare(self):
"""get_rare_data should get only sample X
"""
rare_otu_table = get_rare_data(self.otu_table,
11, include_small_samples=False)
self.assertEqual(rare_otu_table.ids(), ('X',))
# a very complicated way to test things
rare_values = [val[0]
for (val, otu_id, meta) in rare_otu_table.iter(axis='observation')]
self.assertEqual(rare_values, [1.0, 5.0, 3.0, 2.0])
class TopLevelTests(TestCase):
"""Tests of top-level functions"""
def setUp(self):
"""define some top-level data"""
self.otu_table_values = array([[0, 0, 9, 5, 3, 1],
[1, 5, 4, 0, 3, 2],
[2, 3, 1, 1, 2, 5]])
{(0, 2): 9.0, (0, 3): 5.0, (0, 4): 3.0, (0, 5): 1.0,
(1, 0): 1.0, (1, 1): 5.0, (1, 2): 4.0, (1, 4): 3.0, (1, 5): 2.0,
(2, 0): 2.0, (2, 1): 3.0, (2, 2): 1.0, (2, 3): 1.0, (2, 4): 2.0, (2, 5): 5.0}
self.otu_table = Table(self.otu_table_values,
['OTU1', 'OTU2', 'OTU3'],
['Sample1', 'Sample2', 'Sample3',
'Sample4', 'Sample5', 'Sample6'],
[{"taxonomy": ['Bacteria']},
{"taxonomy": ['Archaea']},
{"taxonomy": ['Streptococcus']}],
[None, None, None, None, None, None])
self.otu_table_f = Table(self.otu_table_values,
['OTU1', 'OTU2', 'OTU3'],
['Sample1', 'Sample2', 'Sample3',
'Sample4', 'Sample5', 'Sample6'],
[{"taxonomy": ['1A', '1B', '1C', 'Bacteria']},
{"taxonomy":
['2A', '2B', '2C', 'Archaea']},
{"taxonomy": ['3A', '3B', '3C', 'Streptococcus']}],
[None, None, None, None, None, None])
self.full_lineages = [['1A', '1B', '1C', 'Bacteria'],
['2A', '2B', '2C', 'Archaea'],
['3A', '3B', '3C', 'Streptococcus']]
self.metadata = [[['Sample1', 'NA', 'A'],
['Sample2', 'NA', 'B'],
['Sample3', 'NA', 'A'],
['Sample4', 'NA', 'B'],
['Sample5', 'NA', 'A'],
['Sample6', 'NA', 'B']],
['SampleID', 'CAT1', 'CAT2'], []]
self.tree_text = ["('OTU3',('OTU1','OTU2'))"]
fh, self.tmp_heatmap_fpath = mkstemp(prefix='test_heatmap_',
suffix='.pdf')
close(fh)
def test_extract_metadata_column(self):
"""Extracts correct column from mapping file"""
obs = extract_metadata_column(self.otu_table.ids(),
self.metadata, category='CAT2')
exp = ['A', 'B', 'A', 'B', 'A', 'B']
self.assertEqual(obs, exp)
def test_get_order_from_categories(self):
"""Sample indices should be clustered within each category"""
category_labels = ['A', 'B', 'A', 'B', 'A', 'B']
obs = get_order_from_categories(self.otu_table, category_labels)
group_string = "".join([category_labels[i] for i in obs])
self.assertTrue("AAABBB" == group_string or group_string == "BBBAAA")
def test_get_order_from_tree(self):
obs = get_order_from_tree(
self.otu_table.ids(axis='observation'),
self.tree_text)
exp = [2, 0, 1]
assert_almost_equal(obs, exp)
def test_make_otu_labels(self):
lineages = []
for val, id, meta in self.otu_table.iter(axis='observation'):
lineages.append([v for v in meta['taxonomy']])
obs = make_otu_labels(self.otu_table.ids(axis='observation'),
lineages, n_levels=1)
exp = ['Bacteria (OTU1)', 'Archaea (OTU2)', 'Streptococcus (OTU3)']
self.assertEqual(obs, exp)
full_lineages = []
for val, id, meta in self.otu_table_f.iter(axis='observation'):
full_lineages.append([v for v in meta['taxonomy']])
obs = make_otu_labels(self.otu_table_f.ids(axis='observation'),
full_lineages, n_levels=3)
exp = ['1B;1C;Bacteria (OTU1)',
'2B;2C;Archaea (OTU2)',
'3B;3C;Streptococcus (OTU3)']
self.assertEqual(obs, exp)
def test_names_to_indices(self):
new_order = ['Sample4', 'Sample2', 'Sample3',
'Sample6', 'Sample5', 'Sample1']
obs = names_to_indices(self.otu_table.ids(), new_order)
exp = [3, 1, 2, 5, 4, 0]
assert_almost_equal(obs, exp)
def test_get_log_transform(self):
obs = get_log_transform(self.otu_table)
data = [val for val in self.otu_table.iter_data(axis='observation')]
xform = asarray(data, dtype=float64)
for (i, val) in enumerate(obs.iter_data(axis='observation')):
non_zeros = argwhere(xform[i] != 0)
xform[i, non_zeros] = log10(xform[i, non_zeros])
assert_almost_equal(val, xform[i])
def test_get_clusters(self):
data = asarray([val for val in self.otu_table.iter_data(axis='observation')])
obs = get_clusters(data, axis='row')
self.assertTrue([0, 1, 2] == obs or obs == [1, 2, 0])
obs = get_clusters(data, axis='column')
exp = [2, 3, 1, 4, 0, 5]
self.assertEqual(obs, exp)
def test_plot_heatmap(self):
plot_heatmap(
self.otu_table, self.otu_table.ids(axis='observation'),
self.otu_table.ids(), filename=self.tmp_heatmap_fpath)
self.assertEqual(exists(self.tmp_heatmap_fpath), True)
remove_files(set([self.tmp_heatmap_fpath]))