def generate_class_weights(
reference_taxonomy: Series, reference_sequences: DNAIterator,
samples: biom.Table, taxonomy_classification: DataFrame,
unobserved_weight: float = 1e-6, normalise: bool = False,
allow_weight_outside_reference: bool = False) \
-> biom.Table:
weights = {
reference_taxonomy[seq.metadata['id']]: 0.
for seq in reference_sequences
}
if normalise:
samples.norm()
tax_map = taxonomy_classification['Taxon']
try:
taxa = [tax_map[s] for s in samples.ids(axis='observation')]
except KeyError as s:
raise ValueError(str(s) + ' not in taxonomy_classification')
if not allow_weight_outside_reference and not set(taxa).issubset(weights):
raise ValueError(
'taxonomy_classification does not match reference_taxonomy')
for taxon, count in zip(taxa, samples.sum('observation')):
if taxon in weights:
weights[taxon] += count
taxa, weights = zip(*weights.items())
weights = array(weights)
weights /= weights.sum()
weights = \
(1. - unobserved_weight) * weights + unobserved_weight / len(weights)
weights /= weights.sum()
return biom.Table(weights[None].T, taxa, sample_ids=['Weight'])
def rpca(
table: biom.Table,
rank: int = 3,
min_sample_count: int = 500,
min_feature_count: int = 10,
iterations: int = 5
) -> (skbio.OrdinationResults, skbio.DistanceMatrix):
""" Runs RPCA with an rclr preprocessing step"""
# filter sample to min depth
def sample_filter(val, id_, md):
return sum(val) > min_sample_count
table = table.filter(sample_filter, axis='sample')
table = table.to_dataframe().T.drop_duplicates()
table = table.T[table.sum() > min_feature_count].T
# rclr preprocessing and OptSpace (RPCA)
opt = OptSpace(rank=rank, iteration=iterations).fit(rclr().fit_transform(
table.copy()))
rename_cols = {i - 1: 'PC' + str(i) for i in range(1, rank + 1)}
# Feature Loadings
feature_loading = pd.DataFrame(opt.feature_weights, index=table.columns)
feature_loading = feature_loading.rename(columns=rename_cols)
feature_loading.sort_values('PC1', inplace=True, ascending=True)
# Sample Loadings
sample_loading = pd.DataFrame(opt.sample_weights, index=table.index)
sample_loading = sample_loading.rename(columns=rename_cols)
# % var explained
proportion_explained = pd.Series(opt.explained_variance_ratio,
index=list(rename_cols.values()))
# eigan-vals
eigvals = pd.Series(opt.eigenvalues, index=list(rename_cols.values()))
# if the rank is two add PC3 of zeros
if rank == 2:
feature_loading['PC3'] = [0] * len(feature_loading.index)
sample_loading['PC3'] = [0] * len(sample_loading.index)
eigvals.loc['PC3'] = 0
proportion_explained.loc['PC3'] = 0
# save ordination results
short_method_name = 'rpca_biplot'
long_method_name = '(Robust Aitchison) RPCA Biplot'
ord_res = skbio.OrdinationResults(
short_method_name,
long_method_name,
eigvals.copy(),
samples=sample_loading.copy(),
features=feature_loading.copy(),
proportion_explained=proportion_explained.copy())
# save distance matrix
dist_res = skbio.stats.distance.DistanceMatrix(opt.distance,
ids=sample_loading.index)
return ord_res, dist_res
def cluster_features(query_table: biom.Table, closed_reference_table: biom.Table,
query_sequences: DNAFASTAFormat,
reference_sequences: pd.Series, thr: float = 0.97,
threads: int = 1, output_log_file: str = None) -> (
biom.Table, DNAFASTAFormat, DNAFASTAFormat):
reference_sequences_fasta = get_reference_seqs_from_ids(closed_reference_table, reference_sequences)
results = cluster_features_closed_reference(sequences=query_sequences, table=query_table,
reference_sequences=reference_sequences_fasta,
perc_identity=thr, threads=threads)
clustered_table_biom = results[0]
clustered_sequences_pd = Artifact.load(str(results[1])).view(pd.Series)
unmatched_sequences_pd = Artifact.load(str(results[2])).view(pd.Series)
with tempfile.mktemp() as tmp_fp:
logger_ins = LOG(tmp_fp).get_logger('clustering_features')
logger_ins.info("The number of OTUs in the reference database is", _15(reference_sequences_fasta).size)
logger_ins.info("The number of unmatched sequence to the reference alignment is", unmatched_sequences_pd.size)
logger_ins.info("The number of matched sequences to the reference alignment is", clustered_sequences_pd.size)
logger_ins.info("Before applying clustering, the total number of counts "
"in the original feature table was", np.sum(query_table.sum()))
logger_ins.info("Before applying clustering, the number of non-zero elements"
" of the underlying feature table is", query_table.nnz)
logger_ins.info("After applying clustering, the total number of counts "
"in the original feature table was", np.sum(clustered_table_biom.sum()))
logger_ins.info("After applying clustering, the number of non-zero elements"
" of the underlying feature table is", clustered_table_biom.nnz)
logger_ins.info("The percent of total counts retained is",
np.sum(query_table.sum()) / np.sum(clustered_table_biom.sum()) * 100, "%s")
query_samples = clustered_table_biom.ids('sample')
closed_reference_features = closed_reference_table.ids('observation')
clustered_table_biom = closed_reference_table.merge(clustered_table_biom)
clustered_table_biom.filter(ids_to_keep=query_samples, axis='sample', inplace=True)
if len(set(closed_reference_features) - set(clustered_table_biom.ids('sample'))) != 0:
raise ValueError(
"Merging two tables failed! There are less features in the final table than expected!"
)
if output_log_file:
shutil.copy(tmp_fp, output_log_file)
return clustered_table_biom, results[1], results[2]
def __init__(self,
table: biom.Table,
metadata: pd.DataFrame = None,
batch_category: str = None):
super(BiomDataset).__init__()
if np.any(table.sum(axis='sample') <= 0):
ValueError('Biom table has zero counts.')
self.table = table
self.metadata = metadata
self.batch_category = batch_category
self.populate()
def alpha_rarefaction(output_dir: str,
table: biom.Table,
max_depth: int,
phylogeny: skbio.TreeNode = None,
metrics: set = None,
metadata: qiime2.Metadata = None,
min_depth: int = 1,
steps: int = 10,
iterations: int = 10) -> None:
if metrics is None:
metrics = {'observed_otus', 'shannon'}
if phylogeny is not None:
metrics.add('faith_pd')
elif not metrics:
raise ValueError('`metrics` was given an empty set.')
else:
phylo_overlap = phylogenetic_metrics() & metrics
if phylo_overlap and phylogeny is None:
raise ValueError('Phylogenetic metric %s was requested but '
'phylogeny was not provided.' % phylo_overlap)
if max_depth <= min_depth:
raise ValueError('Provided max_depth of %d must be greater than '
'provided min_depth of %d.' % (max_depth, min_depth))
possible_steps = max_depth - min_depth
if possible_steps < steps:
raise ValueError('Provided number of steps (%d) is greater than the '
'steps possible between min_depth and '
'max_depth (%d).' % (steps, possible_steps))
if table.is_empty():
raise ValueError('Provided table is empty.')
max_frequency = max(table.sum(axis='sample'))
if max_frequency < max_depth:
raise ValueError('Provided max_depth of %d is greater than '
'the maximum sample total frequency of the '
'feature_table (%d).' % (max_depth, max_frequency))
if metadata is None:
columns, filtered_columns = set(), set()
else:
# Filter metadata to only include sample IDs present in the feature
# table. Also ensures every feature table sample ID is present in the
# metadata.
metadata = metadata.filter_ids(table.ids(axis='sample'))
# Drop metadata columns that aren't categorical, or consist solely of
# missing values.
pre_filtered_cols = set(metadata.columns)
metadata = metadata.filter_columns(column_type='categorical',
drop_all_missing=True)
filtered_columns = pre_filtered_cols - set(metadata.columns)
metadata_df = metadata.to_dataframe()
metadata_df.columns = pd.MultiIndex.from_tuples([
(c, '') for c in metadata_df.columns
])
columns = metadata_df.columns.get_level_values(0)
data = _compute_rarefaction_data(table, min_depth, max_depth, steps,
iterations, phylogeny, metrics)
filenames = []
for m, data in data.items():
metric_name = quote(m)
filename = '%s.csv' % metric_name
if metadata is None:
n_df = _compute_summary(data, 'sample-id')
jsonp_filename = '%s.jsonp' % metric_name
_alpha_rarefaction_jsonp(output_dir, jsonp_filename, metric_name,
n_df, '')
filenames.append(jsonp_filename)
else:
merged = data.join(metadata_df, how='left')
for column in columns:
column_name = quote(column)
reindexed_df, counts = _reindex_with_metadata(
column, columns, merged)
c_df = _compute_summary(reindexed_df, column, counts=counts)
jsonp_filename = "%s-%s.jsonp" % (metric_name, column_name)
_alpha_rarefaction_jsonp(output_dir, jsonp_filename,
metric_name, c_df, column)
filenames.append(jsonp_filename)
with open(os.path.join(output_dir, filename), 'w') as fh:
data.columns = [
'depth-%d_iter-%d' % (t[0], t[1]) for t in data.columns.values
]
if metadata is not None:
data = data.join(metadata.to_dataframe(), how='left')
data.to_csv(fh, index_label=['sample-id'])
index = os.path.join(TEMPLATES, 'alpha_rarefaction_assets', 'index.html')
q2templates.render(index,
output_dir,
context={
'metrics': list(metrics),
'filenames': [quote(f) for f in filenames],
'columns': list(columns),
'steps': steps,
'filtered_columns': sorted(filtered_columns)
})
shutil.copytree(
os.path.join(TEMPLATES, 'alpha_rarefaction_assets', 'dist'),
os.path.join(output_dir, 'dist'))
def ctf_helper(
table: biom.Table,
sample_metadata: DataFrame,
individual_id_column: str,
state_columns: list,
n_components: int = DEFAULT_COMP,
min_sample_count: int = DEFAULT_MSC,
min_feature_count: int = DEFAULT_MFC,
max_iterations_als: int = DEFAULT_MAXITER,
max_iterations_rptm: int = DEFAULT_MAXITER,
n_initializations: int = DEFAULT_MAXITER,
feature_metadata: DataFrame = DEFFM
) -> (dict, OrdinationResults, dict, tuple):
""" Runs Compositional Tensor Factorization CTF.
"""
# validate the metadata using q2 as a wrapper
if sample_metadata is not None and not isinstance(sample_metadata,
DataFrame):
sample_metadata = sample_metadata.to_dataframe()
keep_cols = state_columns + [individual_id_column]
all_sample_metadata = sample_metadata.drop(keep_cols, axis=1)
sample_metadata = sample_metadata[keep_cols]
# validate the metadata using q2 as a wrapper
if feature_metadata is not None and not isinstance(feature_metadata,
DataFrame):
feature_metadata = feature_metadata.to_dataframe()
# match the data (borrowed in part from gneiss.util.match)
subtablefids = table.ids('observation')
subtablesids = table.ids('sample')
if len(subtablesids) != len(set(subtablesids)):
raise ValueError('Data-table contains duplicate sample IDs')
if len(subtablefids) != len(set(subtablefids)):
raise ValueError('Data-table contains duplicate feature IDs')
submetadataids = set(sample_metadata.index)
subtablesids = set(subtablesids)
subtablefids = set(subtablefids)
if feature_metadata is not None:
submetadatafeat = set(feature_metadata.index)
fidx = subtablefids & submetadatafeat
if len(fidx) == 0:
raise ValueError(("No more features left. Check to make "
"sure that the sample names between "
"`feature-metadata` and `table` are "
"consistent"))
feature_metadata = feature_metadata.reindex(fidx)
sidx = subtablesids & submetadataids
if len(sidx) == 0:
raise ValueError(("No more features left. Check to make sure that "
"the sample names between `sample-metadata` and"
" `table` are consistent"))
if feature_metadata is not None:
table.filter(list(fidx), axis='observation', inplace=True)
table.filter(list(sidx), axis='sample', inplace=True)
sample_metadata = sample_metadata.reindex(sidx)
# filter and import table
for axis, min_sum in zip(['sample', 'observation'],
[min_sample_count, min_feature_count]):
table = table.filter(table.ids(axis)[table.sum(axis) >= min_sum],
axis=axis,
inplace=True)
# table to dataframe
table = DataFrame(table.matrix_data.toarray(), table.ids('observation'),
table.ids('sample'))
# tensor building
tensor = build()
tensor.construct(table, sample_metadata, individual_id_column,
state_columns)
# factorize
TF = TensorFactorization(n_components=n_components,
max_als_iterations=max_iterations_als,
max_rtpm_iterations=max_iterations_rptm,
n_initializations=n_initializations).fit(
rclr(tensor.counts))
# label tensor loadings
TF.label(tensor, taxonomy=feature_metadata)
# if the n_components is two add PC3 of zeros
# this is referenced as in issue in
# <https://github.com/biocore/emperor/commit
# /a93f029548c421cb0ba365b4294f7a5a6b0209ce>
if n_components == 2:
TF.subjects.loc[:, 'PC3'] = [0] * len(TF.subjects.index)
TF.features.loc[:, 'PC3'] = [0] * len(TF.features.index)
TF.proportion_explained['PC3'] = 0
TF.eigvals['PC3'] = 0
# save ordination results
short_method_name = 'CTF_Biplot'
long_method_name = 'Compositional Tensor Factorization Biplot'
# only keep PC -- other tools merge metadata
keep_PC = [col for col in TF.features.columns if 'PC' in col]
subj_ordin = OrdinationResults(
short_method_name,
long_method_name,
TF.eigvals,
samples=TF.subjects[keep_PC].dropna(axis=0),
features=TF.features[keep_PC].dropna(axis=0),
proportion_explained=TF.proportion_explained)
# save distance matrix for each condition
distances = {}
state_ordn = {}
subject_trajectories = {}
feature_trajectories = {}
for condition, cond, dist, straj, ftraj in zip(tensor.conditions,
TF.conditions,
TF.subject_distances,
TF.subject_trajectory,
TF.feature_trajectory):
# match distances to metadata
ids = straj.index
ind_dict = dict((ind, ind_i) for ind_i, ind in enumerate(ids))
inter = set(ind_dict).intersection(sample_metadata.index)
indices = sorted([ind_dict[ind] for ind in inter])
dist = dist[indices, :][:, indices]
distances[condition] = skbio.stats.distance.DistanceMatrix(
dist, ids=ids[indices])
# fix conditions
if n_components == 2:
cond['PC3'] = [0] * len(cond.index)
cond = OrdinationResults(short_method_name,
long_method_name,
TF.eigvals,
samples=cond[keep_PC].dropna(axis=0),
features=TF.features[keep_PC].dropna(axis=0),
proportion_explained=TF.proportion_explained)
state_ordn[condition] = cond
# add the sample metadata before returning output
# addtionally only keep metadata with trajectory
# output available.
pre_merge_cols = list(straj.columns)
straj = concat(
[straj.reindex(all_sample_metadata.index), all_sample_metadata],
axis=1,
sort=True)
straj = straj.dropna(subset=pre_merge_cols)
# ensure index name for q2
straj.index.name = "#SampleID"
# save traj.
keep_PC_traj = [col for col in straj.columns if 'PC' in col]
straj[keep_PC_traj] -= straj[keep_PC_traj].mean()
ftraj[keep_PC_traj] -= ftraj[keep_PC_traj].mean()
subject_trajectories[condition] = straj
ftraj.index = ftraj.index.astype(str)
feature_trajectories[condition] = ftraj
return (state_ordn, subj_ordin, distances, subject_trajectories,
feature_trajectories)
def alpha_rarefaction(output_dir: str, table: biom.Table, max_depth: int,
phylogeny: skbio.TreeNode = None, metrics: set = None,
metadata: qiime2.Metadata = None, min_depth: int = 1,
steps: int = 10, iterations: int = 10) -> None:
if metrics is None:
metrics = {'observed_otus', 'shannon'}
if phylogeny is not None:
metrics.add('faith_pd')
elif not metrics:
raise ValueError('`metrics` was given an empty set.')
else:
phylo_overlap = phylogenetic_metrics() & metrics
if phylo_overlap and phylogeny is None:
raise ValueError('Phylogenetic metric %s was requested but '
'phylogeny was not provided.' % phylo_overlap)
if max_depth <= min_depth:
raise ValueError('Provided max_depth of %d must be greater than '
'provided min_depth of %d.' % (max_depth, min_depth))
possible_steps = max_depth - min_depth
if possible_steps < steps:
raise ValueError('Provided number of steps (%d) is greater than the '
'steps possible between min_depth and '
'max_depth (%d).' % (steps, possible_steps))
if table.is_empty():
raise ValueError('Provided table is empty.')
max_frequency = max(table.sum(axis='sample'))
if max_frequency < max_depth:
raise ValueError('Provided max_depth of %d is greater than '
'the maximum sample total frequency of the '
'feature_table (%d).' % (max_depth, max_frequency))
if metadata is None:
columns, filtered_columns = set(), set()
else:
# Filter metadata to only include sample IDs present in the feature
# table. Also ensures every feature table sample ID is present in the
# metadata.
metadata = metadata.filter_ids(table.ids(axis='sample'))
# Drop metadata columns that aren't categorical, or consist solely of
# missing values.
pre_filtered_cols = set(metadata.columns)
metadata = metadata.filter_columns(column_type='categorical',
drop_all_missing=True)
filtered_columns = pre_filtered_cols - set(metadata.columns)
metadata_df = metadata.to_dataframe()
if metadata_df.empty or len(metadata.columns) == 0:
raise ValueError("All metadata filtered after dropping columns "
"that contained non-categorical data.")
metadata_df.columns = pd.MultiIndex.from_tuples(
[(c, '') for c in metadata_df.columns])
columns = metadata_df.columns.get_level_values(0)
data = _compute_rarefaction_data(table, min_depth, max_depth,
steps, iterations, phylogeny, metrics)
filenames = []
for m, data in data.items():
metric_name = quote(m)
filename = '%s.csv' % metric_name
if metadata is None:
n_df = _compute_summary(data, 'sample-id')
jsonp_filename = '%s.jsonp' % metric_name
_alpha_rarefaction_jsonp(output_dir, jsonp_filename, metric_name,
n_df, '')
filenames.append(jsonp_filename)
else:
merged = data.join(metadata_df, how='left')
for column in columns:
column_name = quote(column)
reindexed_df, counts = _reindex_with_metadata(column,
columns,
merged)
c_df = _compute_summary(reindexed_df, column, counts=counts)
jsonp_filename = "%s-%s.jsonp" % (metric_name, column_name)
_alpha_rarefaction_jsonp(output_dir, jsonp_filename,
metric_name, c_df, column)
filenames.append(jsonp_filename)
with open(os.path.join(output_dir, filename), 'w') as fh:
data.columns = ['depth-%d_iter-%d' % (t[0], t[1])
for t in data.columns.values]
if metadata is not None:
data = data.join(metadata.to_dataframe(), how='left')
data.to_csv(fh, index_label=['sample-id'])
index = os.path.join(TEMPLATES, 'alpha_rarefaction_assets', 'index.html')
q2templates.render(index, output_dir,
context={'metrics': list(metrics),
'filenames': [quote(f) for f in filenames],
'columns': list(columns),
'steps': steps,
'filtered_columns': sorted(filtered_columns)})
shutil.copytree(os.path.join(TEMPLATES, 'alpha_rarefaction_assets',
'dist'),
os.path.join(output_dir, 'dist'))
def alpha_rarefaction(output_dir: str, table: biom.Table, max_depth: int,
phylogeny: skbio.TreeNode=None, metrics: set=None,
metadata: qiime2.Metadata=None, min_depth: int=1,
steps: int=10, iterations: int=10) -> None:
if metrics is None:
metrics = {'observed_otus', 'shannon'}
if phylogeny is not None:
metrics.add('faith_pd')
elif not metrics:
raise ValueError('`metrics` was given an empty set.')
else:
phylo_overlap = phylogenetic_metrics() & metrics
if phylo_overlap and phylogeny is None:
raise ValueError('Phylogenetic metric %s was requested but '
'phylogeny was not provided.' % phylo_overlap)
if max_depth <= min_depth:
raise ValueError('Provided max_depth of %d must be greater than '
'provided min_depth of %d.' % (max_depth, min_depth))
possible_steps = max_depth - min_depth
if possible_steps < steps:
raise ValueError('Provided number of steps (%d) is greater than the '
'steps possible between min_depth and '
'max_depth (%d).' % (steps, possible_steps))
if table.is_empty():
raise ValueError('Provided table is empty.')
max_frequency = max(table.sum(axis='sample'))
if max_frequency < max_depth:
raise ValueError('Provided max_depth of %d is greater than '
'the maximum sample total frequency of the '
'feature_table (%d).' % (max_depth, max_frequency))
if metadata is not None:
metadata_ids = metadata.ids()
table_ids = set(table.ids(axis='sample'))
if not table_ids.issubset(metadata_ids):
raise ValueError('Missing samples in metadata: %r' %
table_ids.difference(metadata_ids))
filenames, categories, empty_columns = [], [], []
data = _compute_rarefaction_data(table, min_depth, max_depth,
steps, iterations, phylogeny, metrics)
for m, data in data.items():
metric_name = quote(m)
filename = '%s.csv' % metric_name
if metadata is None:
n_df = _compute_summary(data, 'sample-id')
jsonp_filename = '%s.jsonp' % metric_name
_alpha_rarefaction_jsonp(output_dir, jsonp_filename, metric_name,
n_df, '')
filenames.append(jsonp_filename)
else:
metadata_df = metadata.to_dataframe()
metadata_df = metadata_df.loc[data.index]
all_columns = metadata_df.columns
metadata_df.dropna(axis='columns', how='all', inplace=True)
empty_columns = set(all_columns) - set(metadata_df.columns)
metadata_df.columns = pd.MultiIndex.from_tuples(
[(c, '') for c in metadata_df.columns])
merged = data.join(metadata_df, how='left')
categories = metadata_df.columns.get_level_values(0)
for category in categories:
category_name = quote(category)
reindexed_df, counts = _reindex_with_metadata(category,
categories,
merged)
c_df = _compute_summary(reindexed_df, category, counts=counts)
jsonp_filename = "%s-%s.jsonp" % (metric_name, category_name)
_alpha_rarefaction_jsonp(output_dir, jsonp_filename,
metric_name, c_df, category_name)
filenames.append(jsonp_filename)
with open(os.path.join(output_dir, filename), 'w') as fh:
data.columns = ['depth-%d_iter-%d' % (t[0], t[1])
for t in data.columns.values]
if metadata is not None:
data = data.join(metadata.to_dataframe(), how='left')
data.to_csv(fh, index_label=['sample-id'])
index = os.path.join(TEMPLATES, 'alpha_rarefaction_assets', 'index.html')
q2templates.render(index, output_dir,
context={'metrics': list(metrics),
'filenames': filenames,
'categories': list(categories),
'empty_columns': sorted(empty_columns)})
shutil.copytree(os.path.join(TEMPLATES, 'alpha_rarefaction_assets',
'dist'),
os.path.join(output_dir, 'dist'))