def test_targets(self):
bam_bc_file = tk_test.in_path("namesort_test.bam")
read_info_out = tk_test.out_path("read_info.h5")
barcode_whitelist = bc_utils.load_barcode_whitelist("737K-april-2014")
targets_filename = tk_test.in_path('agilent_kinome_targs.bed')
targets_file = open(targets_filename, 'r')
target_regions = tk_io.get_target_regions(targets_file)
bam_in = tk_bam.create_bam_infile(bam_bc_file)
r = compute_basic_stats(bam_in,
target_regions,
1000,
bam_in.references,
barcode_whitelist=barcode_whitelist,
read_h5_out=read_info_out)
# insert_size_dists, nearest_targ_dists, summary_metrics, bc_table, mapq_counts, insert_size_hist = r
misc_sm, bc_sms = r
nearest_targ_dists = bc_sms.get('nearest_targ_dists')
maxTargetDist = max(nearest_targ_dists.get_summarizer(60).dict.keys())
minTargetDist = min(nearest_targ_dists.get_summarizer(60).dict.keys())
self.assertEqual(minTargetDist, 130)
self.assertEqual(maxTargetDist, 10000)
def split(args):
if args.bcsorted_bam is None or args.barcode_whitelist is None:
chunk_defs = [{'chunk_start': "0", 'chunk_end': "0"}]
return {'chunks': chunk_defs}
# if args.input
# Some R&D bc sets have very small diversity -- don't run on them
barcode_whitelist = bc_utils.load_barcode_whitelist(args.barcode_whitelist)
if len(barcode_whitelist) < 100:
chunk_defs = [{'chunk_start': "0", 'chunk_end': "0"}]
return {'chunks': chunk_defs}
# if barcode_whitelist
min_chunks = 4
if len(barcode_whitelist) > 1e6:
min_chunks = 8
# if barcode_whitelist
bam_in = tk_bam.create_bam_infile(args.bcsorted_bam)
chunks = tk_bam.chunk_bam_records(bam_in,
chunk_split_func,
chunk_size_gb=8.0,
min_chunks=min_chunks)
for c in chunks:
c['__mem_gb'] = 12
# for c
return {'chunks': chunks, 'join': {'__mem_gb': 32}}
def test_attach_bcs(self):
# --align_input alignment_output.bam --barcode_input phix_I2.fastq --output test2.out --complete ~/c --stats ~/s
args = {
'barcode_whitelist' : IN_WHITELIST,
'align_chunk' : IN_BAM,
'barcode_chunk' : IN_I2,
'sample_index_chunk' : IN_I1,
'gem_group' : None,
'paired_end' : True,
'exclude_non_bc_reads' : False,
'max_expected_bc_error': 0.75,
'subsample_rate' : 1.0,
}
outs = { 'output': OUT_BAM }
args = martian.Record(args)
outs = martian.Record(outs)
main(args, outs)
# Get the barcodes
barcode_whitelist = bc_utils.load_barcode_whitelist(IN_WHITELIST)
# Ensure each read has a barcode
out_bam = pysam.Samfile(OUT_BAM)
for r in out_bam:
tag_dict = { k:v for (k,v) in r.tags }
tag_names = [ k for (k,v) in r.tags ]
self.assertTrue(RAW_BARCODE_TAG in tag_names)
if tag_dict[RAW_BARCODE_TAG] in barcode_whitelist:
self.assertTrue(PROCESSED_BARCODE_TAG in tag_names)
self.assertTrue(SAMPLE_INDEX_TAG in tag_names)
# Make sure we put out the full BAM file
out_len = len([ x for x in pysam.Samfile(OUT_BAM)])
in_len = len([ x for x in pysam.Samfile(IN_BAM)])
self.assertEqual(out_len, in_len)
def get_bc(r):
tags = { k:v for (k,v) in r.tags }
return tags[RAW_BARCODE_TAG]
# Ensure each read pair has the same barcode
out_bam = pysam.Samfile(OUT_BAM)
reads = [ x for x in out_bam ]
for (grp, reads) in groupby(reads, lambda x: x.qname):
bcs = set(crdna_io.get_read_barcode(r) for r in reads)
self.assertEqual(len(bcs), 1)
def split(args):
bam = pysam.Samfile(args.input, check_sq=False)
min_chunks = 1
if args.barcode_whitelist is not None:
barcode_whitelist = bc_utils.load_barcode_whitelist(
args.barcode_whitelist)
if len(barcode_whitelist) > 1e6:
min_chunks = 4
# Split to ensure read pairs always go together
chunks = tk_bam.chunk_bam_records(bam,
lambda x: x.qname,
min_chunks=min_chunks)
for chunk in chunks:
chunk['n_chunks'] = len(chunks)
chunk['__mem_gb'] = 3
return {'chunks': chunks, 'join': {'__mem_gb': 8}}
def main_report_basic(args, outs):
bam_in = pysam.Samfile(args.input, check_sq=False)
targets_filename = args.targets_file
references = bam_in.references
if args.input_pos is not None:
bam_in_pos = tk_bam.create_bam_infile(args.input_pos)
n_mapped = bam_in_pos.mapped
n_chunk = math.ceil(n_mapped / args.n_chunks)
bam_in_pos.close()
else:
n_mapped = 0
n_chunk = 0
if targets_filename is None or targets_filename == '':
target_regions = None
else:
targets_file = open(targets_filename, 'r')
target_regions = tk_io.get_target_regions(targets_file)
if args.barcode_whitelist:
barcode_whitelist = bc_utils.load_barcode_whitelist(
args.barcode_whitelist)
else:
barcode_whitelist = None
bam_slice = tk_bam.read_bam_chunk(bam_in,
(args.chunk_start, args.chunk_end))
# do basic counting
misc_sm, qual_sms = \
compute_basic_stats(bam_slice,
target_regions,
n_chunk,
references,
barcode_whitelist)
misc_sm.save(outs.misc_sm)
with open(outs.qual_sms, 'wb') as out_handle:
pickle.dump(qual_sms, out_handle)
def split(args):
if args.input is None or args.barcode_whitelist is None:
chunk_defs = [{'chunk_start':"0", 'chunk_end':"0"}]
return {'chunks': chunk_defs}
# Some R&D bc sets have very small diversity -- don't run on them
barcode_whitelist = bc_utils.load_barcode_whitelist(args.barcode_whitelist)
if len(barcode_whitelist) < 100:
chunk_defs = [{'chunk_start':"0", 'chunk_end':"0"}]
return {'chunks': chunk_defs}
min_chunks = 20
if len(barcode_whitelist) > 1e6:
min_chunks = 100
bam_in = tk_bam.create_bam_infile(args.input)
chunks = tk_bam.chunk_bam_records(bam_in, groupbybarcode,
chunk_size_gb=8.0, min_chunks=min_chunks)
for c in chunks:
c['__mem_gb'] = 3
return {'chunks': chunks, 'join': {'__mem_gb': 6}}
def test_barcode_counts(self):
bam_bc_file = tk_test.in_path("attach_bcs/attach_bcs_output.bam")
read_info_out = tk_test.out_path("read_info.h5")
barcode_whitelist = bc_utils.load_barcode_whitelist("737K-april-2014")
bam_in = tk_bam.create_bam_infile(bam_bc_file)
r = compute_basic_stats(bam_in, {},
2000,
bam_in.references,
barcode_whitelist=barcode_whitelist,
read_h5_out=read_info_out)
# insert_size_dists, nearest_targ_dists, summary_metrics, bc_table, mapq_counts, insert_size_hist = r
misc_sm, bc_sms = r
# Look at the barcode results -- there should be a raw bc count for each read pair
# n_raw_bcs = bc_table["count"].sum()
n_reads = len([x for x in tk_bam.create_bam_infile(bam_bc_file)])
# self.assertEqual(n_raw_bcs, n_reads / 2)
# Load the per-cluster table -- there should be a row for each read pair
read_info = tenkit.hdf5.read_data_frame(read_info_out)
self.assertEqual(read_info.shape[0], n_reads / 2)
def join(args, outs, chunk_defs, chunk_outs):
''' join the various outputs created by report_basic '''
chunk_outs = list(chunk_outs)
martian.log_info("combining misc summary managers")
misc_sm_outs = [x.misc_sm for x in chunk_outs]
misc_sm = combine_summary_managers(misc_sm_outs)
martian.log_info("combining nested summary managers")
qual_sms_outs = [x.qual_sms for x in chunk_outs]
qual_sms = combine_nested_summary_managers(qual_sms_outs)
martian.log_info("computing summary metrics")
compute_summary_metrics(misc_sm, qual_sms)
metrics = misc_sm.get_summarizer("metrics")
if metrics["unmapped_fract"] > 0.90:
martian.exit("%.1f %% of reads were not mapped to the supplied "\
"reference genome. This is likely the consequence of a sample "\
"mixup or very low sequencing quality. Further execution will "\
"be halted." % (metrics["unmapped_fract"]*100))
if args.barcode_whitelist:
barcode_whitelist = bc_utils.load_barcode_whitelist(
args.barcode_whitelist)
else:
barcode_whitelist = None
# barcode hdf5
if outs.barcode_counts:
bc_table = summarize_barcode_data(misc_sm, qual_sms, barcode_whitelist)
tenkit.hdf5.write_data_frame(outs.barcode_counts, bc_table)
# insert sizes output
insert_size_dists = {}
for qual in INSERT_MAPQ_CUTOFFS:
insert_size_dists[qual] = qual_sms['insert_size_dists'].get_summarizer(
qual).dict
insert_sizes_output_file = open(outs.insert_sizes, 'w')
insert_sizes_output_file.write(
tenkit.safe_json.safe_jsonify(insert_size_dists) + '\n')
insert_sizes_output_file.close()
# target distances
nearest_targ_dists = {}
for qual in TARGET_MAPQ_CUTOFFS:
nearest_targ_dists[qual] = qual_sms[
'nearest_targ_dists'].get_summarizer(qual).dict
target_dists_output_file = open(outs.target_dists, 'w')
target_dists_output_file.write(
tenkit.safe_json.safe_jsonify(nearest_targ_dists))
target_dists_output_file.close()
# overall summary metrics
summary_output_file = open(outs.summary, 'w')
summary_output_file.write(
tenkit.safe_json.safe_jsonify(misc_sm.get_summarizer('metrics').dict,
pretty=True))
summary_output_file.close()
# mapq counts
mapq_output_file = open(outs.mapq_counts, 'w')
mapq_output_file.write(
tenkit.safe_json.safe_jsonify(
misc_sm.get_summarizer('mapq_counts').dict))
mapq_output_file.close()
# logging
print tenkit.safe_json.safe_jsonify(misc_sm.get_summarizer('metrics').dict,
pretty=True)
def join(args, outs, chunk_defs, chunk_outs):
final_chunks = []
for cl in chunk_outs:
final_chunks.extend(cl.chunks)
outs.chunks = final_chunks
valid_counts = [c.bc_counts for c in chunk_outs if c.bc_counts is not None]
# No counts if there's no whitelist or actual counts
if args.barcode_whitelist is None or len(valid_counts) == 0:
outs.bc_counts = None
outs.lot_info = None
return
result = {}
for (c_out, c_def) in zip(chunk_outs, chunk_defs):
gem_group = c_def.chunk['gem_group']
if c_out.bc_counts is None:
continue
with open(c_out.bc_counts) as f:
r = json.load(f)
gg_result = result.setdefault(gem_group, {
'bad_bc_count': 0,
'bc_counts': None
})
gg_result['bad_bc_count'] += r['bad_bc_count']
if gg_result['bc_counts'] is None:
gg_result['bc_counts'] = np.array(r['bc_counts'], dtype=np.int32)
else:
gg_result['bc_counts'] += np.array(r['bc_counts'], dtype=np.int32)
total_counts = 0
total_errors = 0
for gg in result.keys():
rgg = result[gg]
rgg['bc_error_rate'] = tk_stats.robust_divide(
float(rgg['bad_bc_count']),
float(rgg['bad_bc_count'] + rgg['bc_counts'].sum()))
total_counts += float(rgg['bad_bc_count'] + rgg['bc_counts'].sum())
total_errors += float(rgg['bad_bc_count'])
# Hardcoded bail-out if the BC-correct rate is extremely high
bc_error_rate = total_errors / total_counts
if bc_error_rate > 0.97:
martian.exit(
"Extremely high rate of incorrect barcodes observed (%.2f %%). Check that input is 10x Chromium data, and that there are no missing cycles in the first 16bp of Read 1."
% (bc_error_rate * 100.0))
# possibly do lot detection
lot_detection = {}
lot_map = WHITELIST_TO_LOT_MAP.get(args.barcode_whitelist)
if lot_map is not None:
# get BC counts histogram
# for now, just sum over all gem groups
bc_seq = sorted(
list(bc_utils.load_barcode_whitelist(args.barcode_whitelist)))
bc_cts = np.sum([ggr['bc_counts'] for ggr in result.values()], axis=0)
bc_hist = {seq: cts for seq, cts in zip(bc_seq, bc_cts)}
(gelbead_lot, gelbead_lot_confidence,
gelbead_lot_counts) = identify_gelbead_lot(bc_hist, lot_map)
# only report on lots with nonzero counts
gelbead_lot_counts_nonzero = {
lot: count
for lot, count in gelbead_lot_counts.items() if count > 0
}
lot_detection['gelbead_lot'] = gelbead_lot
lot_detection['gelbead_lot_confidence'] = gelbead_lot_confidence
lot_detection['gelbead_lot_counts'] = gelbead_lot_counts_nonzero
martian.log_info("Gelbead lot detected: %s, reason (if None): %s" %
(gelbead_lot, gelbead_lot_confidence))
with open(outs.lot_info, 'w') as f:
tenkit.safe_json.dump_numpy(lot_detection, f, pretty=True)
with open(outs.bc_counts, 'w') as f:
tenkit.safe_json.dump_numpy(result, f)
def main(args, outs):
""" Trim the reads in a series of fasta files """
# Set a fixed random seed to eliminate noise in metrics
random.seed(0)
chunk = args.chunk
interleaved = chunk['reads_interleaved']
have_read2 = chunk['read2'] is not None
paired = interleaved or have_read2
read1_trim = args.read1_trim_length
read2_trim = args.read2_trim_length
subsample_rate = chunk['subsample_rate']
# BC config -- BC come from separate fastq, or are embedded in R1 or R2
have_barcode = False
bc_in_read1 = False
bc_in_read2 = False
bc_in_fastq = False
# If we have bc in read, use that & ignore a separate BC read
if chunk.get('bc_in_read',
None) is not None and chunk.get('bc_length', 0) > 0:
have_barcode = True
bc_length = chunk['bc_length']
if chunk['bc_in_read'] == 1:
bc_in_read1 = True
read1_trim += bc_length
elif chunk['bc_in_read'] == 2:
bc_in_read2 = True
read2_trim += bc_length
else:
martian.exit(
"bc_in_read configuration incorrect -- read must be 1 or 2")
# Otherwise use the BC file
elif chunk['barcode'] is not None:
have_barcode = True
bc_in_fastq = True
have_sample_index = chunk['sample_index'] is not None
have_trim1 = args.read1_trim_length > 0
have_trim2 = args.read2_trim_length > 0
output_directory = os.path.dirname(os.path.realpath(outs.placeholder))
max_read_num = args.max_read_num
# counter for sub-chunked files
file_number = 1
# open the available read files and make the appropriate iterators
if interleaved:
read_in = openfq(chunk['read1'])
read_iter = tk_fasta.read_generator_fastq(read_in, paired_end=True)
else:
if have_read2:
read1_in = openfq(chunk['read1'])
read1_iter = tk_fasta.read_generator_fastq(read1_in)
read2_in = openfq(chunk['read2'])
read2_iter = tk_fasta.read_generator_fastq(read2_in)
read_iter = itertools.imap(
lambda x, y: (x[0], x[1], x[2], y[0], y[1], y[2]), read1_iter,
read2_iter)
else:
read1_in = openfq(chunk['read1'])
read_iter = tk_fasta.read_generator_fastq(read1_in)
# open read file
read_name = output_directory + "/read" + str(file_number) + ".fastq"
read_names = [read_name]
out_read_fastq = open(read_name, 'w')
# Bail out if there's no barcodes or whitelist
if args.barcode_whitelist is None:
outs.bc_counts = None
bc_idx = None
else:
barcode_whitelist = sorted(
list(bc_utils.load_barcode_whitelist(args.barcode_whitelist)))
bc_idx = {bc: idx for (idx, bc) in enumerate(barcode_whitelist)}
bc_counts = np.zeros(len(barcode_whitelist), dtype=np.int32)
bad_count = 0
# open barcode file if there is one
if have_barcode:
bc_name = output_directory + "/BC" + str(file_number) + ".fastq"
out_bc_fastq = open(bc_name, 'w')
bc_names = [bc_name]
if bc_in_fastq:
bc_in = openfq(chunk['barcode'])
bc_iter = tk_fasta.read_generator_fastq(bc_in)
elif bc_in_read1 or bc_in_read2:
# BC in read -- have output file but no input file
bc_iter = itertools.repeat(None)
else:
bc_iter = itertools.repeat(None)
bc_names = [None]
outs.bc_counts = None
# open sample_index file if there is one
if have_sample_index:
si_name = output_directory + "/SI" + str(file_number) + ".fastq"
out_si_fastq = open(si_name, 'w')
si_in = openfq(chunk['sample_index'])
si_iter = tk_fasta.read_generator_fastq(si_in)
si_names = [si_name]
else:
si_iter = itertools.repeat(None)
si_names = [None]
# open trim_read file if there is one
if have_trim1 or have_trim2:
trim_name = output_directory + "/TRIM" + str(file_number) + ".fastq"
out_trim_fastq = open(trim_name, 'w')
trim_names = [trim_name]
else:
trim_names = [None]
# loop through reads
read_num = 0
for read, barcode_read, sample_index_read in itertools.izip(
read_iter, bc_iter, si_iter):
if read_num > 0 and random.random() > subsample_rate:
continue
if paired:
(name1, seq1, qual1, name2, seq2, qual2) = read
else:
(name1, seq1, qual1) = read
if len(seq1) != len(qual1):
martian.exit(
"Invalid FASTQ file: read and qual lengths don't match")
new_seq1 = seq1[read1_trim:]
trim_seq1 = seq1[:read1_trim]
new_qual1 = qual1[read1_trim:]
trim_qual1 = qual1[:read1_trim]
if paired:
if len(seq1) != len(qual1):
martian.exit(
"Invalid FASTQ file: read and qual lengths don't match")
new_seq2 = seq2[read2_trim:]
new_qual2 = qual2[read2_trim:]
trim_seq2 = seq2[:read2_trim]
trim_qual2 = qual2[:read2_trim]
# Get BC sequence out of the read, for BC-in-read schemes
if bc_in_read1:
barcode_read = (name1, seq1[:bc_length], qual1[:bc_length])
trim_seq1 = trim_seq1[bc_length:]
trim_qual1 = trim_qual1[bc_length:]
if bc_in_read2:
barcode_read = (name2, seq2[:bc_length], qual2[:bc_length])
trim_seq2 = trim_seq2[bc_length:]
trim_qual2 = trim_qual2[bc_length:]
read_num += 1
if read_num > max_read_num:
read_num = 1
file_number += 1
read_name = output_directory + "/read" + str(
file_number) + ".fastq"
out_read_fastq.close()
out_read_fastq = open(read_name, 'w')
read_names.append(read_name)
if have_barcode:
bc_name = output_directory + "/BC" + str(
file_number) + ".fastq"
out_bc_fastq.close()
out_bc_fastq = open(bc_name, 'w')
bc_names.append(bc_name)
else:
bc_names.append(None)
if have_trim1 or have_trim2:
trim_name = output_directory + "/TRIM" + str(
file_number) + ".fastq"
out_trim_fastq.close()
out_trim_fastq = open(trim_name, 'w')
trim_names.append(trim_name)
else:
trim_names.append(None)
if have_sample_index:
si_name = output_directory + "/SI" + str(
file_number) + ".fastq"
out_si_fastq.close()
out_si_fastq = open(si_name, 'w')
si_names.append(si_name)
else:
si_names.append(None)
if have_barcode:
barcode_seq = barcode_read[1]
barcode_qual = barcode_read[2]
if chunk['barcode_reverse_complement']:
barcode_seq = tk_seq.get_rev_comp(barcode_seq)
barcode_qual = barcode_qual[::
-1] # obscure way to reverse string
if bc_idx is not None:
idx = bc_idx.get(barcode_seq)
if idx is not None:
bc_counts[idx] += 1
else:
bad_count += 1
tk_fasta.write_read_fastq(out_bc_fastq, barcode_read[0],
barcode_seq, barcode_qual)
if have_sample_index:
tk_fasta.write_read_fastq(out_si_fastq, sample_index_read[0],
sample_index_read[1],
sample_index_read[2])
tk_fasta.write_read_fastq(out_read_fastq, name1, new_seq1, new_qual1)
if have_trim1 or have_trim2:
tk_fasta.write_read_fastq(out_trim_fastq, name1, trim_seq1,
trim_qual1)
if paired:
tk_fasta.write_read_fastq(out_read_fastq, name2, new_seq2,
new_qual2)
if have_trim1 or have_trim2:
tk_fasta.write_read_fastq(out_trim_fastq, name2, trim_seq2,
trim_qual2)
if have_barcode:
out_bc_fastq.close()
# Only emit BC counts if we had a whitelist
if outs.bc_counts is not None:
result = {}
result['bad_bc_count'] = bad_count
result['bc_counts'] = list(bc_counts)
with open(outs.bc_counts, 'w') as bc_counts_out:
tenkit.safe_json.dump_numpy(result, bc_counts_out)
if have_sample_index:
out_si_fastq.close()
if have_trim1 or have_trim2:
out_trim_fastq.close()
out_read_fastq.close()
chunks = []
for (r, bc, si, trim) in zip(read_names, bc_names, si_names, trim_names):
new_chunk = {
'read1': r,
'read2': None,
'barcode': bc,
'sample_index': si,
'trim': trim,
'barcode_reverse_complement': False,
'reads_interleaved': have_read2 or interleaved,
'gem_group': chunk['gem_group'],
'read_group': chunk['read_group']
}
chunks.append(new_chunk)
outs.chunks = chunks
def main(args, outs):
""" Attaches barcodes. Attaches raw barcode to RAW_BC tag and filters those to form set of PROCESSES_BARCODES """
# this silences a weird non-failure in --strict=error mode
# TODO(lhepler): remove this when martian upstream handles this itself
outs.outputs = []
chunk = args.chunk
bam_in = tk_bam.create_bam_infile(args.align_chunk)
bc_spec = "{}:{}".format(RAW_BARCODE_TAG, RAW_BARCODE_QUAL_TAG)
# only comment the first chunk, otherwise later merge will duplicate the comments and could lead to:
# samtools merge ... : '[finish_merged_header] Output header text too long'
if args.chunk_index > 0:
COs = None
elif chunk['trim']:
COs = ['10x_bam_to_fastq:R1({},TR:TQ,SEQ:QUAL)'.format(bc_spec), '10x_bam_to_fastq:R2(SEQ:QUAL)', '10x_bam_to_fastq:I1(BC:QT)']
else:
COs = ['10x_bam_to_fastq:R1({},SEQ:QUAL)'.format(bc_spec), '10x_bam_to_fastq:R2(SEQ:QUAL)', '10x_bam_to_fastq:I1(BC:QT)']
bam_out, tids = tk_bam.create_bam_outfile(outs.output, None, None, template=bam_in, pgs=[tk_bam.make_pg_header(martian.get_pipelines_version(), "attach_bcs")], cos = COs)
gp_tagger = GlobalFivePrimePosTagger(bam_in)
if args.barcode_whitelist is None or args.bc_counts is None:
# If there's no whitelist or counts then all high quality BC reads get allowed.
barcode_whitelist = None
wl_idxs = None
bc_dist = None
else:
barcode_whitelist = bc_utils.load_barcode_whitelist(args.barcode_whitelist)
# Load the bc counts for this GEM group
counts = json.load(open(args.bc_counts, 'r'))
counts = counts[str(chunk['gem_group'])]['bc_counts']
# Prior distribution over barcodes, with pseudo-count
bc_dist = np.array(counts, dtype=np.float) + 1.0
bc_dist = bc_dist / bc_dist.sum()
wl_idxs = { bc:idx for (idx,bc) in enumerate(sorted(list(barcode_whitelist))) }
# set random seed to get deterministic subsampling
random.seed(0)
def open_maybe_gzip(fn):
if fn[-2:] == "gz":
return gzip.open(fn)
else:
return open(fn)
if chunk['barcode']:
processed_barcode_iter = get_raw_processed_barcodes(open_maybe_gzip(chunk['barcode']), barcode_whitelist, args.bc_confidence_threshold, chunk['gem_group'], chunk['barcode_reverse_complement'], wl_idxs, bc_dist)
require_barcode_for_stringent = True
else:
processed_barcode_iter = itertools.repeat(None)
require_barcode_for_stringent = False
if chunk['trim']:
trim_iter = tk_fasta.read_generator_fastq(open_maybe_gzip(chunk['trim']), paired_end=True)
else:
trim_iter = itertools.repeat(None)
if chunk['sample_index']:
sample_index_iter = tk_fasta.read_generator_fastq(open_maybe_gzip(chunk['sample_index']))
else:
sample_index_iter = itertools.repeat(None)
iters = itertools.izip(processed_barcode_iter, sample_index_iter, trim_iter)
# First read
read = bam_in.next()
# Number of perfect reads -- used to compute down-sampling rates in mark_duplicates
perfect_read_count = 0
# Due to secondary alignments, we must apply the tags to all
# reads with the same cluster name.
for (barcode_info, sample_index_info, trim_info) in iters:
tags = []
read_name = None
if read is None:
break
if barcode_info:
(bc_read_name, raw_bc_seq, processed_bc_seq, raw_bc_qual) = barcode_info
tags.append((RAW_BARCODE_TAG, raw_bc_seq))
tags.append((RAW_BARCODE_QUAL_TAG, raw_bc_qual))
if processed_bc_seq is not None:
tags.append((PROCESSED_BARCODE_TAG, processed_bc_seq))
read_name = bc_read_name.split()[0]
if sample_index_info:
(si_read_name, seq, qual) = sample_index_info
tags.append((SAMPLE_INDEX_TAG, seq))
tags.append((SAMPLE_INDEX_QUAL_TAG, qual))
if read_name != None:
if si_read_name.split()[0] != read_name:
martian.log_info("mismatch: si_read_name: %s, bam_read_name: %s" % (si_read_name, read_name))
assert(si_read_name.split()[0] == read_name)
else:
read_name = si_read_name.split()[0]
r1_tags = tags
r2_tags = list(tags)
if trim_info:
(trim1_read_name, trim1_seq, trim1_qual, trim2_read_name, trim2_seq, trim2_qual) = trim_info
if len(trim1_seq) > 0:
r1_tags.append((TRIM_TAG, trim1_seq))
r1_tags.append((TRIM_QUAL_TAG, trim1_qual))
if len(trim2_seq) > 0:
r2_tags.append((TRIM_TAG, trim2_seq))
r2_tags.append((TRIM_QUAL_TAG, trim2_qual))
reads_attached = 0
reads_to_attach = []
while read.qname == read_name or read_name == None:
tags = r1_tags if read.is_read1 else r2_tags
if len(tags) > 0:
existing_tags = read.tags
existing_tags.extend(tags)
read.tags = existing_tags
if not (read_name is None):
assert(read.qname == read_name)
if reads_to_attach and (read.query_name != reads_to_attach[0].query_name or reads_to_attach[0].query_name is None):
gp_tagger.tag_reads(reads_to_attach)
reads_attached += len(reads_to_attach)
for r in reads_to_attach:
if stringent_read_filter(r, require_barcode_for_stringent):
perfect_read_count += 1
if args.exclude_non_bc_reads:
if not(crdna_io.get_read_barcode(r) is None):
bam_out.write(r)
else:
bam_out.write(r)
reads_to_attach = []
reads_to_attach.append(read)
try:
read = bam_in.next()
except StopIteration:
read = None
break
gp_tagger.tag_reads(reads_to_attach)
reads_attached += len(reads_to_attach)
for r in reads_to_attach:
if stringent_read_filter(r, require_barcode_for_stringent):
perfect_read_count += 1
if args.exclude_non_bc_reads:
if not(crdna_io.get_read_barcode(r) is None):
bam_out.write(r)
else:
bam_out.write(r)
# We may have more than 2 reads is there was a
# secondary alignment, but less than 2 means
# something went wrong
assert(reads_attached >= 2)
outs.perfect_read_count = perfect_read_count
bam_out.close()
