def split(args):
ctg_mgr = ReferenceManager(args.reference_path)
species = ctg_mgr.list_species()
if args.filtered_peak_bc_matrix is None or len(species) > 1:
return {'chunks': [{'__mem_gb': h5_constants.MIN_MEM_GB}]}
chunks = []
matrix_mem_gb = 0.
if args.filtered_tf_bc_matrix is not None:
matrix_mem_gb = cr_matrix.CountMatrix.get_mem_gb_from_matrix_h5(args.filtered_tf_bc_matrix) * 1.5
matrix_mem_gb += cr_matrix.CountMatrix.get_mem_gb_from_matrix_h5(args.filtered_peak_bc_matrix)
chunk_mem_gb = int(np.ceil(max(matrix_mem_gb, h5_constants.MIN_MEM_GB)))
if not set(args.factorization).issubset(ALLOWED_FACTORIZATIONS):
raise ValueError('Invalid factorization provided')
# create a chunk for each method x clustering combo
for method in args.factorization:
clustering_h5 = args.clustering_summary['h5'][method]
for key in SingleGenomeAnalysis.load_clustering_keys_from_h5(clustering_h5):
clustering = SingleGenomeAnalysis.load_clustering_from_h5(clustering_h5, key)
for cluster in set(clustering.clusters):
chunks.append({
'method': method,
'clustering_key': key,
'cluster': cluster,
'__mem_gb': chunk_mem_gb,
'__vmem_gb': chunk_mem_gb + int(np.ceil(ctg_mgr.get_vmem_est())) + 1,
'__threads': 1,
})
return {'chunks': chunks, 'join': {'__mem_gb': 3}}
def check_reference_format(reference_path):
"""Check file formats for files present in the reference"""
try:
contig_manager = ReferenceManager(reference_path)
except Exception as e:
martian.exit("Contig manager could not be initialized, Error:\n%s" % str(e))
# formatting
error_msg = contig_manager.verify_contig_defs()
if error_msg is not None:
martian.exit(error_msg)
# filecheck
contig_manager.genes
# check if motif file is in right format (naming convention)
if len(contig_manager.list_species()) == 1:
motif_format_checker(contig_manager.motifs)
# checks for valid bed file formats in regions/
faidx_file = os.path.join(reference_path, 'fasta', 'genome.fa.fai')
bed_format_checker(contig_manager.tss_track, faidx_file)
bed_format_checker(contig_manager.transcripts_track, faidx_file)
bed_format_checker(contig_manager.ctcf_track, faidx_file)
bed_format_checker(contig_manager.blacklist_track, faidx_file)
bed_format_checker(contig_manager.dnase_track, faidx_file)
bed_format_checker(contig_manager.enhancer_track, faidx_file)
bed_format_checker(contig_manager.promoter_track, faidx_file)
def main(args, outs):
'''Find cut sites on a per chromosome basis and write out a bedgraph'''
if args.fragments is None:
outs.count_dict = None
outs.cut_sites = None
return
ctg_mgr = ReferenceManager(args.reference_path)
contig_len = ctg_mgr.get_contig_lengths()
chrom_len = contig_len[args.contig]
half_window = WINDOW_SIZE // 2
Cuts = np.zeros(chrom_len, dtype='int32')
# find windowed cut sites
for _, start, stop, _, _ in parsed_fragments_from_contig(contig=args.contig, filename=args.fragments, index=args.fragments_index):
Cuts[max(0, start - half_window): min(start + half_window + 1, chrom_len)] += 1
Cuts[max(0, stop - half_window): min(stop + half_window + 1, chrom_len)] += 1
# get count dict
count_dict = Counter(v for v in Cuts if v > 0)
with open(outs.count_dict, 'w') as count_dict_out:
pickle.dump(count_dict, count_dict_out)
# write bedgraph of * windowed cutsites *
if len(count_dict):
write_chrom_bedgraph(args.contig, chrom_len, Cuts, outs.cut_sites)
else:
outs.cut_sites = None
def main(args, outs):
metrics = {}
for fname in args.metrics:
if fname is not None:
with open(fname, 'r') as f:
metrics.update(json.load(f))
# Normalize "NaN" values
for key in metrics:
value = metrics[key]
if str(value) == 'NaN' or (isinstance(value, float) and np.isnan(value)):
metrics[key] = None
# add version info
metrics['cellranger-atac_version'] = martian.get_pipelines_version()
if len(metrics) > 0:
martian.log_info('Writing out summary_metrics')
with open(outs.metrics, 'w') as outfile:
outfile.write(tenkit.safe_json.safe_jsonify(metrics, pretty=True))
# compile summary.csv metrics
# load library info and fake libraries as species
metric_registry = MetricAnnotations()
metrics_csv_dict = {}
if args.library_info is not None:
with open(args.library_info, 'r') as f:
library_info = pickle.load(f)
library_list = [library_info[n]['library_id'] for n in library_info.keys()]
metrics_csv_dict.update(metric_registry.compile_summary_metrics(metrics, species_list=library_list))
# load species level metrics
ctg_mgr = ReferenceManager(args.reference_path)
metrics_csv_dict.update(metric_registry.compile_summary_metrics(metrics, species_list=ctg_mgr.list_species()))
write_dict_to_csv(outs.metrics_csv, metrics_csv_dict, sort=True)
def split(args):
"""Compute base background in split and use it in each chunk."""
ref_mgr = ReferenceManager(args.reference_path)
npeaks = utils.quick_line_count(args.peaks) if args.peaks else 0
if len(ref_mgr.list_species()
) > 1 or npeaks == 0 or ref_mgr.motifs is None:
chunk_def = [{'skip': True}]
return {'chunks': chunk_def}
with open(args.globalGCdict, 'r') as f:
GCdict = pickle.load(f)
GCdict_paths = {}
GCbins = sorted(GCdict.keys())
for gc in GCbins:
GCdict_paths[gc] = martian.make_path('GCdict_{}_{}'.format(
gc[0], gc[1]))
with open(GCdict_paths[gc], 'w') as dump:
pickle.dump(GCdict[gc], dump)
# write rows of each chunk to a new peak file
mem_in_gb = 8
chunk_def = [{
'__mem_gb':
mem_in_gb,
'__vmem_gb':
mem_in_gb + int(np.ceil(ref_mgr.get_vmem_est())) + 1,
'skip':
False,
'GCdict':
GCdict_paths[chunk]
} for chunk in GCbins]
return {'chunks': chunk_def}
def join(args, outs, chunk_defs, chunk_outs):
ref_mgr = ReferenceManager(args.reference_path)
if args.filtered_matrix is None or args.peak_motif_hits is None or len(
ref_mgr.list_species()) > 1:
outs.filtered_tf_bc_matrix = None
outs.filtered_tf_bc_matrix_mex = None
outs.tf_propZ_matrix = None
return
# motif scan is completed in ANNOTATE_PEAKS
peaks = BedTool(args.peaks)
motifs = Motifs(args.reference_path)
peak_motif_hits = BedTool(args.peak_motif_hits)
# extract peak coordinate to numerical index map
peak_idx, n_peaks = _get_peak_indexes(peaks)
# extract motif names to numerical index map
motif_idx, n_motifs = _get_motif_indexes(motifs)
# extract 3 lists: peak indexes, motif indexes and counts, each entry correspond to a peak-motif pair
peak_coor, motif_coor, values = motifscan_bed_to_sparse_matrix(
peak_motif_hits, peak_idx, motif_idx, format='binary')
# convert it to a sparse matrix, default is binary format, motifs are rows and peaks are columns
tf_peak_matrix = sp.csr_matrix((values, (motif_coor, peak_coor)),
shape=(n_motifs, n_peaks),
dtype='int32')
# compute the motif-BC matrix via pooling
# The current method simply counts the number of hits for a motif inside the peaks in a barcode
# cast as a CountMatrix
peak_matrix = cr_matrix.CountMatrix.load_h5_file(args.filtered_matrix)
motif_names = motif_idx.keys()
barcodes = peak_matrix.bcs
genomes = utils.generate_genome_tag(args.reference_path)
motifs_def = atac_feature_ref.from_motif_list(motif_names, genomes)
tf_matrix = cr_matrix.CountMatrix(motifs_def, barcodes,
tf_peak_matrix * peak_matrix.m)
# perform MAD-zscoring of proportion values
propZ_matrix = np.array(tf_matrix.m / peak_matrix.m.sum(axis=0))
propZ_matrix = MADzscore(propZ_matrix)
outs.coerce_strings()
# save to h5 and csv
tf_matrix.save_h5_file(outs.filtered_tf_bc_matrix,
sw_version=martian.get_pipelines_version())
if not os.path.exists(outs.filtered_tf_bc_matrix_mex):
os.mkdir(outs.filtered_tf_bc_matrix_mex)
atac_matrix.save_mex(
tf_matrix,
outs.filtered_tf_bc_matrix_mex,
feature_type=cr_lib_constants.ATACSEQ_LIBRARY_DERIVED_TYPE,
sw_version=martian.get_pipelines_version())
# save propZ matrix as gz
np.savetxt(outs.tf_propZ_matrix, propZ_matrix)
def generate_genome_tag(ref_path):
"""Replace empty genome name for single genomes with valid genome name"""
# For a single species reference, use contents of <reference_path>/genome
ref_contig_manager = ReferenceManager(ref_path)
genomes = ref_contig_manager.list_species()
if len(genomes) == 1 and genomes[0] == '' or len(genomes) == 0:
genomes = [ref_contig_manager.genome]
return genomes
def main(args, outs):
reference = ReferenceManager(args.reference_path)
species_list = reference.list_species()
is_barnyard = len(species_list) > 1 and args.singlecell is not None
summary_data = None
if args.summary_results:
with open(args.summary_results, 'r') as infile:
summary_data = json.load(infile)
# Pull up the correct template information
template_path = os.path.dirname(os.path.abspath(__file__))
template_file = os.path.join(
template_path,
'{}{}.html'.format('barnyard' if is_barnyard else 'single',
'_debug' if args.debug else ''))
with open(template_file, 'r') as infile:
template = infile.read()
metadata = MetricAnnotations()
websummary_data = {
'alarms': {
'alarms': []
},
'sample': {
'id': args.sample_id,
'description': args.sample_desc,
'pipeline': "Cell Ranger ATAC Renalyzer"
}
}
singlecell_df = pd.read_csv(
args.singlecell) if args.singlecell is not None else None
add_data(
websummary_data,
get_hero_metric_data(metadata, summary_data, species_list, args.debug))
add_data(websummary_data, get_pipeline_info(args, reference, args.debug))
add_data(
websummary_data,
get_clustering_plots(metadata, summary_data, args.analysis,
args.filtered_peak_bc_matrix, species_list,
singlecell_df, is_barnyard))
# Modify the titles of plots to add consistent plot styling sample ID/descriptions
for key, subdata in websummary_data.iteritems():
if "layout" in subdata:
subdata["layout"][
"title"] += '<br><sup>Sample {} - {}</sup>'.format(
args.sample_id, args.sample_desc)
subdata["layout"]["hovermode"] = "closest"
subdata["config"] = PLOT_CONFIG_KWARGS
with open(outs.web_summary, 'w') as outfile:
summarize.generate_html_summary(websummary_data, template,
template_path, outfile)
def split(args):
ref_mgr = ReferenceManager(args.reference_path)
return {
'chunks': [],
'join': {
'__mem_gb': 4,
'__vmem_gb': int(np.ceil(ref_mgr.get_vmem_est())) + 3
}
}
def main(args, outs):
if args.singlecell_mapping is None or args.singlecell_targets is None or args.singlecell_cells is None:
outs.singlecell = None
outs.summary = None
return
ref = ReferenceManager(args.reference_path)
species_list = ref.list_species()
# Merge the input singlecell data into a single dataframe and write it out
mapping = pd.read_csv(args.singlecell_mapping)
cells = pd.read_csv(args.singlecell_cells)
targeting = pd.read_csv(args.singlecell_targets)
merged = mapping.merge(cells,
how="left",
on="barcode",
sort=False,
validate="one_to_one")
merged["cell_id"] = merged["cell_id"].fillna("None")
for column in merged.columns:
if column.endswith("_cell_barcode") or column.startswith(
"passed_filters_") or column.startswith(
"peak_region_fragments_"):
merged[column] = merged[column].fillna(0).astype(int)
merged = merged.merge(targeting,
how="left",
on="barcode",
sort=False,
validate="one_to_one")
keys = [
"{}_fragments".format(region) for region in [
"TSS", "DNase_sensitive_region", "enhancer_region",
"promoter_region", "on_target", "blacklist_region", "peak_region"
]
] + ["peak_region_cutsites"]
for column in keys:
merged[column] = merged[column].fillna(0).astype(int)
merged.to_csv(outs.singlecell, index=None)
summary_info = {}
summary_info = add_bulk_targeting_metrics(summary_info, merged,
species_list)
summary_info = add_doublet_rate_metrics(summary_info, merged, species_list)
summary_info = add_purity_metrics(summary_info, merged, species_list)
summary_info = add_bulk_mapping_metrics(summary_info, merged, species_list)
summary_info = add_singlecell_sensitivity_metrics(summary_info, merged,
species_list)
with open(outs.summary, 'w') as summary_file:
summary_file.write(json.dumps(summary_info, indent=4))
def split(args):
if args.fragments is None:
return {"chunks": [], "join": {}}
ctg_mgr = ReferenceManager(args.reference_path)
all_contigs = ctg_mgr.primary_contigs(allow_sex_chromosomes=True)
chunks = []
for contig in all_contigs:
chunks.append({"contig": contig, "__mem_gb": 5})
return {"chunks": chunks, "join": {"__mem_gb": 5}}
def split(args):
if args.fragments is None:
return {'chunks': [], 'join': {}}
ctg_mgr = ReferenceManager(args.reference_path)
all_contigs = ctg_mgr.primary_contigs(allow_sex_chromosomes=True)
chunks = []
for contig in all_contigs:
chunks.append({'contig': contig, '__mem_gb': 5})
return {'chunks': chunks, 'join': {'__mem_gb': 5}}
def join(args, outs, chunk_defs, chunk_outs):
ctg_mgr = ReferenceManager(args.reference_path)
species = ctg_mgr.list_species()
if args.filtered_peak_bc_matrix is None or len(species) > 1:
outs.enrichment_analysis = None
outs.enrichment_analysis_summary = {}
return
peak_matrix_features = cr_matrix.CountMatrix.load_feature_ref_from_h5_file(args.filtered_peak_bc_matrix)
tf_matrix_features = cr_matrix.CountMatrix.load_feature_ref_from_h5_file(args.filtered_tf_bc_matrix) if args.filtered_tf_bc_matrix is not None else None
outs.enrichment_analysis_summary = {'h5': {}, 'csv': {}}
# for each method, we merge h5 files and copy csv directories to one place
cr_io.mkdir(outs.enrichment_analysis, allow_existing=True)
for method in args.factorization:
method_dir = os.path.join(outs.enrichment_analysis, method)
cr_io.mkdir(method_dir, allow_existing=True)
_h5 = os.path.join(method_dir, '{}_enrichment_h5.h5'.format(method))
outs.enrichment_analysis_summary['h5'][method] = _h5
chunk_h5s = []
_csv = os.path.join(method_dir, '{}_enrichment_csv'.format(method))
outs.enrichment_analysis_summary['csv'][method] = _csv
diffexp_prefixes = [(fr.id, fr.name) for fr in peak_matrix_features.feature_defs]
if args.filtered_tf_bc_matrix is not None:
diffexp_prefixes += [(fr.id, fr.name) for fr in tf_matrix_features.feature_defs]
clustering_h5 = args.clustering_summary['h5'][method]
for key in SingleGenomeAnalysis.load_clustering_keys_from_h5(clustering_h5):
chunk_outs_def_method_clustering = sorted([[chunk_out, chunk_def] for
chunk_out, chunk_def in zip(chunk_outs, chunk_defs)
if chunk_def.clustering_key == key], key=lambda x: x[1].cluster)
chunk_outs_method_clustering = [c[0] for c in chunk_outs_def_method_clustering]
# load 1 vs rest tests in sorted order of chunks and combine into one output per clustering
diffexp = cr_diffexp.DIFFERENTIAL_EXPRESSION(np.hstack([np.loadtxt(com.tmp_diffexp, delimiter=',')[:, 0:3] for com in chunk_outs_method_clustering]))
# write out h5
chunk_h5 = martian.make_path('{}_enrichment_h5.h5'.format(key))
with analysis_io.open_h5_for_writing(chunk_h5) as f:
cr_diffexp.save_differential_expression_h5(f, key, diffexp)
chunk_h5s += [chunk_h5]
# write out csv
cr_diffexp.save_differential_expression_csv_from_features(key, diffexp, diffexp_prefixes, _csv)
analysis_io.combine_h5_files(chunk_h5s, _h5, [analysis_constants.ANALYSIS_H5_DIFFERENTIAL_EXPRESSION_GROUP,
analysis_constants.ANALYSIS_H5_MAP_DE[method]])
def get_cell_barcodes(filename, ref, with_species=False):
"""Read singlecell.csv and emit barcodes"""
scdf = pd.read_csv(filename, sep=',')
ctg_mgr = ReferenceManager(ref)
if not with_species:
cell_barcodes = set()
for species in ctg_mgr.list_species():
species_cell_mask = scdf['is_{}_cell_barcode'.format(species)] == 1
cell_barcodes.update(scdf[species_cell_mask]['barcode'].values.tolist())
else:
cell_barcodes = {}
for species in ctg_mgr.list_species():
species_cell_mask = scdf['is_{}_cell_barcode'.format(species)] == 1
cell_barcodes[species] = set(scdf[species_cell_mask]['barcode'].values.tolist())
return cell_barcodes
def split(args):
if args.fragments is None:
return {'chunks': [], 'join': {}}
ctg_mgr = ReferenceManager(args.reference_path)
all_contigs = ctg_mgr.primary_contigs(allow_sex_chromosomes=True)
contig_len = ctg_mgr.get_contig_lengths()
BYTES_PER_INT32_WITH_SAFETY = 5
chunks = []
for contig in all_contigs:
chunks.append({'contig': contig,
'__mem_gb': int(np.ceil(BYTES_PER_INT32_WITH_SAFETY * contig_len[contig] / 1024 / 1024 / 1024))})
return {'chunks': chunks, 'join': {'__mem_gb': 5}}
def split(args):
if args.fragments is None:
return {"chunks": [], "join": {}}
ctg_mgr = ReferenceManager(args.reference_path)
all_contigs = ctg_mgr.primary_contigs(allow_sex_chromosomes=True)
with open(args.barcode_counts, "r") as infile:
barcode_counts = Counter(json.load(infile))
barcode_array = np.array([bc for bc in barcode_counts])
gem_group_array = np.array(
[get_barcode_gem_group(bc) for bc in barcode_counts])
gem_groups = set(gem_group_array)
frag_count_array = np.array([barcode_counts[bc] for bc in barcode_array])
valid_barcodes = list()
for gem_group in gem_groups:
count_mask = (frag_count_array > MINIMUM_COUNTS) & (gem_group_array
== gem_group)
# find at most top N barcodes
topN_indices = barcode_array[count_mask].argsort(
)[-min(MAXIMUM_BARCODES, len(count_mask)):]
valid_barcodes.extend(list(barcode_array[count_mask][topN_indices]))
# mem allocs
JOIN_LOAD_FACTOR = 2
BUFFER_GB = 2
BYTES_PER_ENTRY = 4 # this depends on the dtype
chunk_mem_gb = BUFFER_GB + np.ceil(
BYTES_PER_ENTRY * len(gem_groups) * MAXIMUM_BARCODES**2 /
1024**3).astype('int32')
join_mem_gb = BUFFER_GB + np.ceil(
JOIN_LOAD_FACTOR * BYTES_PER_ENTRY * len(gem_groups) *
MAXIMUM_BARCODES**2 / 1024**3).astype('int32')
valid_barcodes_path = martian.make_path("valid_barcodes.txt")
with open(valid_barcodes_path, 'w') as f:
f.write(",".join(valid_barcodes))
chunks = []
for contig in all_contigs:
chunks.append({
"contig": contig,
"valid_barcodes": valid_barcodes_path,
"__mem_gb": chunk_mem_gb,
})
return {"chunks": chunks, "join": {"__mem_gb": join_mem_gb}}
def main(args, outs):
"""Downsample each fragments file to produce a sorted file, while computing the pre and post complexity metrics"""
with open(args.library_info, 'r') as f:
library_info = pickle.load(f)[args.n]
# read cells
cell_barcodes = get_cell_barcodes(library_info['cells'],
args.reference_path)
# get chrom key from fasta index
chrom_order = {}
ctg_mgr = ReferenceManager(args.reference_path)
with open(ctg_mgr.fasta_index, 'r') as f:
for en, line in enumerate(f):
chrom = line.split('\t')[0]
chrom_order[chrom] = en
downsampling_metrics = subsample_fragments(
infile=library_info['fragments'],
rate=library_info['rate'],
outfile=outs.fragments,
group=args.n,
cells=cell_barcodes,
kind=library_info['kind'],
key=chrom_order)
with open(outs.normalization_metrics, 'w') as f:
json.dump(downsampling_metrics, f, indent=4)
def split(args):
if args.fragments is None:
return {'chunks': [], 'join': {}}
if args.peaks is None:
martian.throw("peaks BED file expected")
if args.cell_barcodes is None:
martian.throw("cell barcodes CSV file expected")
ctg_mgr = ReferenceManager(args.reference_path)
all_contigs = ctg_mgr.primary_contigs(allow_sex_chromosomes=True)
chunks = []
for contig in all_contigs:
chunks.append({'contig': contig, '__mem_gb': 4})
return {'chunks': chunks, 'join': {'__mem_gb': 8}}
def main(args, outs):
args.coerce_strings()
outs.coerce_strings()
with open(args.barcodes, 'r') as barcode_file:
barcodes_dict = OrderedDict(
(bc.strip('\n'), num) for num, bc in enumerate(barcode_file))
outs.insert_summary = None
if args.fragments is None or len(barcodes_dict) == 0:
outs.insert_sizes = None
outs.total = None
return
ref_contig_manager = ReferenceManager(args.reference_path)
# iterate over fragments and count fragment sizes for each barcode
insert_sizes = {bc: Counter() for bc in barcodes_dict.iterkeys()}
primary_contigs = set(
ref_contig_manager.primary_contigs(allow_sex_chromosomes=True))
for contig, start, stop, barcode, _ in open_fragment_file(args.fragments):
if barcode not in barcodes_dict:
continue
if args.exclude_non_nuclear and contig not in primary_contigs:
continue
size = stop - start
insert_sizes[barcode][
str(size) if size <= MAX_INSERT_SIZE else GT_MAX_INSERT_SIZE] += 1
# compute total and write out csv
total = np.zeros(MAX_INSERT_SIZE)
with open(outs.insert_sizes, 'w') as outfile:
outfile.write(','.join(['Barcode'] +
[str(n)
for n in range(1, MAX_INSERT_SIZE + 1)] +
['>{}'.format(MAX_INSERT_SIZE)]) + '\n')
for barcode in insert_sizes:
outfile.write(','.join([barcode] + [
str(insert_sizes[barcode][str(n)])
for n in range(1, MAX_INSERT_SIZE + 1)
] + [str(insert_sizes[barcode][GT_MAX_INSERT_SIZE])]) + '\n')
for n in range(1, 1001):
total[n - 1] += insert_sizes[barcode][str(n)]
# write out totals for reduce in join
np.savetxt(outs.total, total, delimiter=',')
def get_barcode_gc(ref_f, peaks_f, matrix):
"""Get mean GC% of peaks in a barcode"""
ref_mgr = ReferenceManager(ref_f)
genome_fa = pyfasta.Fasta(ref_mgr.fasta, key_fn=lambda x: x.split()[0])
peak_GC = np.array([get_peak_GC_counts(peak, genome_fa, counts=False)
for peak in peak_reader(peaks_f)])
barcode_GC = ((peak_GC * matrix.m) / np.array(matrix.m.sum(axis=0))).squeeze()
return barcode_GC
def split(args):
"""Compute base background in split and use it in each chunk
"""
n_peaks = utils.quick_line_count(args.peaks) if args.peaks else 0
ref_mgr = ReferenceManager(args.reference_path)
if len(ref_mgr.list_species()) > 1 or n_peaks == 0 or ref_mgr.tss_track is None:
chunk_def = [{'skip': True}]
return {'chunks': chunk_def}
# write rows of each chunk to a new peak file
mem_in_gb = 4.0
chunk_def = [{'__mem_gb': mem_in_gb,
'skip': False,
'chunk_start': chunk[0],
'chunk_end': chunk[1]} for chunk in utils.get_chunks(n_peaks, chunks=20)]
return {'chunks': chunk_def}
def count_bases_in_peaks(reference_path, peaks_file):
"""Count the total number of bases in peak regions (0-indexed)"""
bases_in_peaks = 0
ctg_mgr = ReferenceManager(reference_path)
genome_fa = pyfasta.Fasta(ctg_mgr.fasta, key_fn=lambda x: x.split()[0])
for peak in peak_reader(peaks_file):
bases_in_peaks += len(genome_fa[peak.chrom][peak.start:peak.end])
return bases_in_peaks
def main(args, outs):
"""Run this for each method x clustering key combination from split"""
ctg_mgr = ReferenceManager(args.reference_path)
species = ctg_mgr.list_species()
if args.filtered_peak_bc_matrix is None or len(species) > 1:
return
# Load the peak-BC matrix and a clustering and perform DE
peak_matrix = cr_matrix.CountMatrix.load_h5_file(args.filtered_peak_bc_matrix)
clustering_h5 = args.clustering_summary['h5'][args.method]
clustering = SingleGenomeAnalysis.load_clustering_from_h5(clustering_h5, args.clustering_key)
mask = clustering.clusters == args.cluster
clustering.clusters[mask] = 1
clustering.clusters[np.logical_not(mask)] = 2
# find depth using peak matrix and normalize
scale = np.array(peak_matrix.m.sum(axis=0)).squeeze()
depth = (scale + 1) / np.median(scale)
cov_peak = [np.log(depth)]
diffexp_peak = nb2_diffexp.run_differential_expression(peak_matrix.m, clustering.clusters, model='poisson',
impute_rest=True, test_params={'cov': cov_peak}, verbose=True)
# find empirical estimates of alpha
tf_matrix = None
diffexp_tf = None
# do DE on tf-BC matrix
if args.filtered_tf_bc_matrix is not None:
tf_matrix = cr_matrix.CountMatrix.load_h5_file(args.filtered_tf_bc_matrix)
ntfmatrix = normalize_matrix(tf_matrix.m, scale)
alpha_tf = nb2_diffexp.empirical_dispersion(ntfmatrix)
barcode_GC = get_barcode_gc(args.reference_path, args.peaks, peak_matrix)
cov_tf = [barcode_GC, np.log(depth)]
diffexp_tf = nb2_diffexp.run_differential_expression(tf_matrix.m, clustering.clusters, model='nb', impute_rest=True,
test_params={'cov': cov_tf, 'alpha': alpha_tf}, verbose=True)
# vstack
diffexp = diffexp_peak if tf_matrix is None else cr_diffexp.DIFFERENTIAL_EXPRESSION(np.vstack([diffexp_peak.data, diffexp_tf.data]))
# write out temp file
np.savetxt(outs.tmp_diffexp, diffexp.data, delimiter=',')
outs.enrichment_analysis = None
outs.enrichment_analysis_summary = None
def split(args):
ref_mgr = ReferenceManager(args.reference_path)
if args.filtered_matrix is None or args.peak_motif_hits is None or len(
ref_mgr.list_species()) > 1:
return {'chunks': []}
matrix_mem_gb = cr_matrix.CountMatrix.get_mem_gb_from_matrix_h5(
args.filtered_matrix)
npeaks, nbcs, nnz = cr_matrix.CountMatrix.load_dims_from_h5(
args.filtered_matrix)
# assume we will never test more than 1000 TFs and
# the relative hit-rate of a TF is a generous 1 out of every 10 peaks
MAX_TF_COUNT = 1000
MAX_TF_PEAK_SPARSITY = 0.1
BYTES_PER_INT = np.dtype(int).itemsize
BYTES_PER_FLOAT = np.dtype(float).itemsize
BYTES_PER_GB = 1024**3
ENTRIES_PER_VAL = 3
predicted_tf_peak_matrix_mem_gb = ENTRIES_PER_VAL * MAX_TF_PEAK_SPARSITY * npeaks * MAX_TF_COUNT * BYTES_PER_INT / BYTES_PER_GB
predicted_tf_matrix_mem_gb = ENTRIES_PER_VAL * nbcs * MAX_TF_COUNT * BYTES_PER_INT / BYTES_PER_GB
predicted_tf_propZ_matrix_mem_gb = ENTRIES_PER_VAL * nbcs * MAX_TF_COUNT * BYTES_PER_FLOAT / BYTES_PER_GB
chunk_mem_gb = int(
np.ceil(
max(
matrix_mem_gb + predicted_tf_peak_matrix_mem_gb * 2 +
predicted_tf_matrix_mem_gb * 2 +
predicted_tf_propZ_matrix_mem_gb * 2,
h5_constants.MIN_MEM_GB)))
vmem_peak_motif_hits = int(
np.ceil(predicted_tf_peak_matrix_mem_gb) * 3 +
predicted_tf_peak_matrix_mem_gb)
# HACK - give big jobs more threads in order to avoid overloading a node
threads = cr_io.get_thread_request_from_mem_gb(chunk_mem_gb)
return {
'chunks': [],
'join': {
'__mem_gb': chunk_mem_gb,
'__vmem_gb': chunk_mem_gb + vmem_peak_motif_hits + 1,
'__threads': threads
}
}
def __init__(self, ref_path, bg=None):
ref_manager = ReferenceManager(ref_path)
self.all_motifs = []
if ref_manager.motifs is not None:
with open(ref_manager.motifs, "r") as infile:
self.all_motifs = list(motifs.parse(infile, "jaspar"))
# for large sequence header, only keep the text before the first space
self.genome_seq = pyfasta.Fasta(ref_manager.fasta,
key_fn=lambda x: x.split()[0])
self.bg = bg
def split(args):
"""We just align each chunk independently -- joining will happen in the join step of SORT_READS"""
# Pull some reads from fastq files -- bail out if it's less than 25bp
fastq_tests = [x['read1'] for x in args.chunks]
for fastq_test in fastq_tests:
with open(fastq_test) as in_file:
reader = tk_fasta.read_generator_fastq(in_file)
for name, read, qual in itertools.islice(reader, 10):
if len(read) < MIN_READ_LENGTH:
martian.alarm("BWA-MEM can't handle reads <25bp -- reads will be unmapped.")
continue
# estimated amount of memory needed to process genome is 2x(num gigabases)+4GB
ctg_mgr = ReferenceManager(args.reference_path)
base_mem_in_gb = int(math.ceil(2 * ctg_mgr.get_vmem_est()))
mem_in_gb = base_mem_in_gb + 4
chunks = [{'chunk': x, '__threads': args.num_threads, '__mem_gb': mem_in_gb} for x in args.chunks]
return {'chunks': chunks}
def annotate_peaks(peaks, ref_path):
"""
peak to gene annotation strategy:
1. if a peak overlaps with promoter region (-1kb, + 100) of any TSS, call it a promoter peak
2. if a peak is within 200kb of the closest TSS, AND if it is not a promoter peak, call it a distal peak
3. if a peak overlaps of a transcript, AND it is not a promoter nor a distal peak of the gene, call it a distal peak
This step is optional
4. call it an intergenic peak
"""
ref_mgr = ReferenceManager(ref_path)
tss = BedTool(ref_mgr.tss_track)
# if tss.bed contains the 7th column (gene type), then apply filter. Otherwise use all tss sites
if tss.field_count() == 7:
tss_filtered = tss.filter(lambda x: x[6] in TRANSCRIPT_ANNOTATION_GENE_TYPES).saveas()
else:
df_tss = tss.to_dataframe()
df_tss['gene_type'] = '.'
tss_filtered = BedTool.from_dataframe(df_tss).saveas()
# including transcripts.bed is optional
if ref_mgr.transcripts_track is None:
transcripts_filtered = BedTool([])
else:
transcripts = BedTool(ref_mgr.transcripts_track)
if transcripts.field_count() == 7:
transcripts_filtered = transcripts.filter(lambda x: x[6] in TRANSCRIPT_ANNOTATION_GENE_TYPES).saveas()
else:
df_tx = transcripts.to_dataframe()
df_tx['gene_type'] = '.'
transcripts_filtered = BedTool.from_dataframe(df_tx).saveas()
# run bedtools closest for peaks against filtered tss, group by peaks and summarize annotations from select columns
peaks_nearby_tss = peaks.closest(tss_filtered, D='b', g=ref_mgr.fasta_index).groupby(g=[1, 2, 3], c=[7, 11], o=['collapse']).saveas()
results = []
peaks_nearby_tss_butno_tx = peaks_nearby_tss.intersect(transcripts_filtered, v=True).saveas()
# avoid error when no peaks overlap with any transcipts
if len(peaks_nearby_tss_butno_tx) < len(peaks_nearby_tss):
peaks_nearby_tss_and_tx = peaks_nearby_tss \
.intersect(transcripts_filtered, wa=True, wb=True) \
.groupby(g=[1, 2, 3, 4, 5], c=[9], o=['distinct'])
for peak in peaks_nearby_tss_and_tx:
results.append(get_peak_nearby_genes(peak))
for peak in peaks_nearby_tss_butno_tx:
results.append(get_peak_nearby_genes(peak))
return results
def split(args):
"""split into a chunk for each library in aggr csv, and define a unique gem group"""
aggr_df = pd.read_csv(args.aggr_csv, sep=',')
nchunks = len(aggr_df)
ctg_mgr = ReferenceManager(args.reference_path)
max_contig_len = max(ctg_mgr.get_contig_lengths().values())
BYTES_PER_INT32_WITH_SAFETY = 5
mem_gb = 2 * int(
np.ceil(
BYTES_PER_INT32_WITH_SAFETY * max_contig_len / 1024 / 1024 / 1024))
return {
'chunks': [{
'n': group,
'__mem_gb': mem_gb,
'__vmem_gb': mem_gb + 6
} for group in range(nchunks)],
'join': {
'__mem_gb': 12
}
}
def join(args, outs, chunk_defs, chunk_outs):
"""Compute base background in each peak."""
ref_mgr = ReferenceManager(args.reference_path)
npeaks = utils.quick_line_count(args.peaks) if args.peaks else 0
if len(ref_mgr.list_species()
) > 1 or npeaks == 0 or ref_mgr.motifs is None:
outs.GCdist = None
return
# get peak-GC distribution
genome_fa = pyfasta.Fasta(ref_mgr.fasta, key_fn=lambda x: x.split()[0])
GCdist = [
utils.get_peak_GC_counts(peak, genome_fa, counts=False)
for peak in peak_reader(args.peaks)
]
# compute base background from peaks in bins
# merge extreme GC bins with adjoining ones if they're too narrow for motif scanner to work correctly
GCbounds = []
nbins = NBINS
for n, gc in enumerate(
np.percentile(GCdist,
np.linspace(0, 100, nbins + 1, endpoint=True),
interpolation='lower')):
if n == 0 or n == nbins:
GCbounds += [gc]
continue
if gc >= LOW_GC and gc < HIGH_GC:
GCbounds += [gc]
GCbins = sorted(list(set(zip(GCbounds, GCbounds[1:])))) # uniqify
peaks = peak_reader(args.peaks)
GCdict = get_GCbinned_peaks_and_bg(peaks, genome_fa, GCbins)
# dump
with open(outs.GCdict, 'w') as f:
pickle.dump(GCdict, f)
def split(args):
if args.fragments is None:
return {"chunks": [], "join": {}}
with open(args.barcode_counts, "r") as infile:
barcode_counts = Counter(json.load(infile))
valid_barcodes = barcode_counts.keys()
part_a_seqs, part_c_seqs, part_b_seqs, gem_group_seqs = query_barcode_subsequences(
valid_barcodes)
ctg_mgr = ReferenceManager(args.reference_path)
all_contigs = ctg_mgr.primary_contigs(allow_sex_chromosomes=True)
chunks = []
for gem_group in gem_group_seqs:
for contig in all_contigs:
chunks.append({
"contig": contig,
"gem_group": gem_group,
"__mem_gb": 4,
})
return {"chunks": chunks, "join": {"__mem_gb": 16}}
