formed; reference_index.rname_lengths[RNAME] is the length of RNAME.'''
reference_index = bowtie_index.BowtieIndexReference(
os.path.expandvars(args.bowtie_idx)
)
# For mapping sample indices back to original sample labels
manifest_object = manifest.LabelsAndIndices(os.path.expandvars(args.manifest))
# To convert sample-rname index to sample index-rname index tuple
sample_and_rname_indexes = SampleAndRnameIndexes(
manifest_object,
args.output_by_chromosome
)
import time
start_time = time.time()
from alignment_handlers import AlignmentPrinter
alignment_printer = AlignmentPrinter(manifest_object, reference_index,
tie_margin=args.tie_margin)
input_line_count = 0
if args.suppress_bam:
# Just grab stats
if args.output_by_chromosome:
for (index, _), xpartition in xstream(sys.stdin, 2):
sample_index, rname_index = (
sample_and_rname_indexes.sample_and_rname_indexes(index)
)
unique_count, total_count = 0, 0
for record in xpartition:
if not (int(record[2]) & 256):
total_count += 1
try:
# seq is at position 8
if alignment_printer.unique(record, seq_index=8):
'''Now collect other arguments. While the variable args declared below is
global, properties of args are also arguments of the go() function so
different command-line arguments can be passed to it for unit tests.'''
args = parser.parse_args(argv[1:])
reference_index = bowtie_index.BowtieIndexReference(
os.path.expandvars(args.bowtie_idx))
manifest_object = manifest.LabelsAndIndices(os.path.expandvars(args.manifest))
alignment_count_to_report, seed, non_deterministic \
= bowtie.parsed_bowtie_args(bowtie_args)
alignment_printer = AlignmentPrinter(manifest_object,
reference_index,
output_stream=sys.stdout,
bin_size=args.partition_length,
exon_ivals=args.exon_intervals,
exon_diffs=args.exon_differentials,
drop_deletions=args.drop_deletions,
output_bam_by_chr=args.output_bam_by_chr,
tie_margin=args.tie_margin)
input_line_count, output_line_count = 0, 0
start_time = time.time()
for (qname, ), xpartition in xstream(sys.stdin, 1):
alignments = [(qname, ) + alignment for alignment in xpartition]
input_line_count += len(alignments)
intron_counts = [alignment[5].count('N') for alignment in alignments]
min_intron_count = min(intron_counts)
if not min_intron_count:
'''There is at least one alignment that overlaps no introns; report
an alignment with the highest score at random. Separate into alignments
def go(input_stream=sys.stdin, output_stream=sys.stdout, bowtie2_exe='bowtie2',
bowtie_index_base='genome', bowtie2_index_base='genome2',
manifest_file='manifest', bowtie2_args=None, bin_size=10000, verbose=False,
exon_differentials=True, exon_intervals=False, report_multiplier=1.2,
min_exon_size=8, search_filter=1, min_readlet_size=15, max_readlet_size=25,
readlet_interval=12, capping_multiplier=1.5, drop_deletions=False,
gzip_level=3, scratch=None, index_count=1, output_bam_by_chr=False,
tie_margin=0, no_realign=False, no_polyA=False):
""" Runs Rail-RNA-align_reads.
A single pass of Bowtie is run to find end-to-end alignments. Unmapped
reads are saved for readletizing to determine junctions in sucessive
reduce steps as well as for realignment in a later map step.
Input (read from stdin)
----------------------------
Tab-delimited input tuple columns in a mix of any of the following
three formats:
Format 1 (single-end, 3-column):
1. Nucleotide sequence or its reversed complement, whichever is first
in alphabetical order
2. 1 if sequence was reverse-complemented else 0
3. Name
4. Quality sequence or its reverse, whichever corresponds to field 1
Format 2 (paired, 2 lines, 3 columns each)
(so this is the same as single-end)
1. Nucleotide sequence for mate 1 or its reversed complement,
whichever is first in alphabetical order
2. 1 if sequence was reverse-complemented else 0
3. Name for mate 1
4. Quality sequence for mate 1 or its reverse, whichever corresponds
to field 1
(new line)
1. Nucleotide sequence for mate 2 or its reversed complement,
whichever is first in alphabetical order
2. 1 if sequence was reverse complemented else 0
3. Name for mate 2
4. Quality sequence for mate 2 or its reverse, whichever corresponds
to field 1
Input is partitioned and sorted by field 1, the read sequence.
Hadoop output (written to stdout)
----------------------------
A given RNAME sequence is partitioned into intervals ("bins") of some
user-specified length (see partition.py).
Exonic chunks (aka ECs; three formats, any or all of which may be
emitted):
Format 1 (exon_ival); tab-delimited output tuple columns:
1. Reference name (RNAME in SAM format) + ';' + bin number
2. Sample index
3. EC start (inclusive) on forward strand
4. EC end (exclusive) on forward strand
Format 2 (exon_diff); tab-delimited output tuple columns:
1. Reference name (RNAME in SAM format) + ';' + bin number
2. max(EC start, bin start) (inclusive) on forward strand IFF diff is
positive and EC end (exclusive) on forward strand IFF diff is
negative
3. Sample index
4. '1' if alignment from which diff originates is "unique" according to
--tie-margin criterion; else '0'
5. +1 or -1 * count, the number of instances of a read sequence for
which to print exonic chunks
Note that only unique alignments are currently output as ivals and/or
diffs.
Format 3 (sam); tab-delimited output tuple columns:
Standard SAM output except fields are in different order, and the first
field corresponds to sample label. (Fields are reordered to facilitate
partitioning by sample name/RNAME and sorting by POS.) Each line
corresponds to a spliced alignment. The order of the fields is as
follows.
1. Sample index if outputting BAMs by sample OR
sample-rname index if outputting BAMs by chr
2. (Number string representing RNAME; see BowtieIndexReference
class in bowtie_index for conversion information) OR
'0' if outputting BAMs by chr
3. POS
4. QNAME
5. FLAG
6. MAPQ
7. CIGAR
8. RNEXT
9. PNEXT
10. TLEN
11. SEQ
12. QUAL
... + optional fields
Insertions/deletions (indel_bed)
tab-delimited output tuple columns:
1. 'I' or 'D' insertion or deletion line
2. Number string representing RNAME
3. Start position (Last base before insertion or
first base of deletion)
4. End position (Last base before insertion or last base of deletion
(exclusive))
5. Inserted sequence for insertions or deleted sequence for deletions
6. Sample index
----Next fields are for junctions only; they are '\x1c' for indels----
7. '\x1c'
8. '\x1c'
--------------------------------------------------------------------
9. Number of instances of insertion or deletion in sample; this is
always +1 * count before bed_pre combiner/reducer
Read whose primary alignment is not end-to-end
Tab-delimited output tuple columns (unmapped):
1. Transcriptome Bowtie 2 index group number
2. SEQ
3. 1 if SEQ is reverse-complemented, else 0
4. QNAME
5. QUAL
Tab-delimited output tuple columns (readletized):
1. Readlet sequence or its reversed complement, whichever is first in
alphabetical order
2. read sequence ID + ('-' if readlet
sequence is reverse-complemented; else '+') + '\x1e' + displacement
of readlet's 5' end from read's 5' end + '\x1e' + displacement of
readlet's 3' end from read's 3' end (+, for EXACTLY one readlet of
a read sequence, '\x1e' + read sequence + '\x1e' +
(an '\x1f'-separated list A of unique sample labels with read
sequences that match the original read sequence) + '\x1e' +
(an '\x1f'-separated list of unique sample labels B with read
sequences that match the reversed complement of the original read
sequence)) + '\x1e' + (an '\x1f'-separated list of the number of
instances of the read sequence for each respective sample in list
A) + '\x1e' + (an '\x1f'-separated list of the number of instances
of the read sequence's reversed complement for each respective
sample in list B). Here, a read sequence ID takes the form X:Y,
where X is the "mapred_task_partition" environment variable -- a
unique index for a task within a job -- and Y is the index of the
read sequence relative to the beginning of the input stream.
Tab-delimited tuple columns (postponed_sam):
Standard 11+ -column raw SAM output
Single column (unique):
1. A unique read sequence
Two columns, exactly one line (dummy); ensures creation of junction
index:
1. character "-"
2. the word "dummy"
ALL OUTPUT COORDINATES ARE 1-INDEXED.
input_stream: where to find input reads.
output_stream: where to emit exonic chunks and junctions.
bowtie2_exe: filename of Bowtie2 executable; include path if not in
$PATH.
bowtie_index_base: the basename of the Bowtie1 index files associated
with the reference.
bowtie2_index_base: the basename of the Bowtie2 index files associated
with the reference.
manifest_file: filename of manifest
bowtie2_args: string containing precisely extra command-line arguments
to pass to first-pass Bowtie2.
bin_size: genome is partitioned in units of bin_size for later load
balancing.
verbose: True iff more informative messages should be written to
stderr.
exon_differentials: True iff EC differentials are to be emitted.
exon_intervals: True iff EC intervals are to be emitted.
report_multiplier: if verbose is True, the line number of an alignment
or read written to stderr increases exponentially with base
report_multiplier.
min_exon_size: minimum exon size searched for in junction_search.py
later in pipeline; used to determine how large a soft clip on one
side of a read is necessary to pass it on to junction search
pipeline
search_filter: how large a soft clip on one side of a read is necessary
to pass it on to junction search pipeline
min_readlet_size: "capping" readlets (that is, readlets that terminate
at a given end of the read) are never smaller than this value
max_readlet_size: size of every noncapping readlet
readlet_interval: number of bases separating successive readlets along
the read
capping_multiplier: successive capping readlets on a given end of a
read are increased in size exponentially with base
capping_multiplier
drop_deletions: True iff deletions should be dropped from coverage
vector
gzip_level: compression level to use for temporary files
scratch: scratch directory for storing temporary files or None if
securely created temporary directory
index_count: number of transcriptome Bowtie 2 indexes to which to
assign unmapped reads for later realignment
output_bam_by_chr: True iff final output BAMs will be by chromosome
tie_margin: allowed score difference per 100 bases among ties in
max score. For example, 150 and 144 are tied alignment scores
for a 100-bp read when --tie-margin is 6.
no_realign: True iff job flow does not need more than readlets: this
usually means only a transcript index is being constructed
no_polyA: kill noncapping readlets that are all As and write as
unmapped all reads with polyA prefixes whose suffixes are <
min_exon_size
No return value.
"""
global _input_line_count
reference_index = bowtie_index.BowtieIndexReference(bowtie_index_base)
manifest_object = manifest.LabelsAndIndices(manifest_file)
alignment_printer = AlignmentPrinter(
manifest_object,
reference_index,
bin_size=bin_size,
output_stream=output_stream,
exon_ivals=exon_intervals,
exon_diffs=exon_differentials,
drop_deletions=drop_deletions,
output_bam_by_chr=output_bam_by_chr,
tie_margin=tie_margin
)
# Get task partition to pass to align_reads_delegate.py
try:
task_partition = os.environ['mapred_task_partition']
except KeyError:
# Hadoop 2.x?
try:
task_partition = os.environ['mapreduce_task_partition']
except KeyError:
# A unit test is probably being run
task_partition = '0'
temp_dir = make_temp_dir(scratch)
register_cleanup(tempdel.remove_temporary_directories, [temp_dir])
align_file = os.path.join(temp_dir, 'first_pass_reads.temp.gz')
other_reads_file = os.path.join(temp_dir, 'other_reads.temp.gz')
second_pass_file = os.path.join(temp_dir, 'second_pass_reads.temp.gz')
k_value, _, _ = bowtie.parsed_bowtie_args(bowtie2_args)
nothing_doing = True
# Required length of prefix after poly(A) is trimmed
remaining_seq_size = max(min_exon_size - 1, 1)
with xopen(True, align_file, 'w', gzip_level) as align_stream, \
xopen(True, other_reads_file, 'w', gzip_level) as other_stream:
for seq_number, ((seq,), xpartition) in enumerate(
xstream(sys.stdin, 1)
):
seq_length = len(seq)
if no_polyA and (
all(seq[i] == 'A'
for i in xrange(seq_length - remaining_seq_size))
or all(seq[i] == 'T'
for i in xrange(remaining_seq_size, seq_length))
or all(seq[i] == 'A'
for i in xrange(remaining_seq_size, seq_length))
or all(seq[i] == 'T'
for i in xrange(seq_length - remaining_seq_size))
):
if not no_realign:
'''If a sequence is too short without its poly(A) tail,
make all reads with that sequence unmapped. Technically,
this also kills poly(A)s at 5' ends, but we probably
couldn't align those sequences anyway.'''
reversed_complement_seq = seq[::-1].translate(
_reversed_complement_translation_table
)
for is_reversed, name, qual in xpartition:
if is_reversed == '0':
alignment_printer.print_unmapped_read(
name,
seq,
qual
)
else:
alignment_printer.print_unmapped_read(
name,
reversed_complement_seq,
qual[::-1]
)
continue
nothing_doing = False
'''Select highest-quality read with alphabetically last qname
for first-pass alignment.'''
best_name, best_mean_qual, best_qual_index, i = None, None, 0, 0
others_to_print = dlist()
for is_reversed, name, qual in xpartition:
_input_line_count += 1
others_to_print.append(
'\t'.join([
str(seq_number), is_reversed, name, qual
])
)
mean_qual = (
float(sum([ord(score) for score in qual])) / len(qual)
)
if (mean_qual > best_mean_qual
or mean_qual == best_mean_qual and name > best_name):
best_qual_index = i
best_mean_qual = mean_qual
best_name = name
to_align = '\t'.join([
'%s\x1d%s' % (is_reversed, name),
seq, qual
])
i += 1
assert i >= 1
if i == 1:
print >>other_stream, str(seq_number)
else:
for j, other_to_print in enumerate(others_to_print):
if j != best_qual_index:
print >>other_stream, other_to_print
print >>align_stream, to_align
# Print dummy line
print 'dummy\t-\tdummy'
sys.stdout.flush() # this is REALLY important b/c called script will stdout
if nothing_doing:
# No input
sys.exit(0)
input_command = 'gzip -cd %s' % align_file
bowtie_command = ' '.join([bowtie2_exe,
bowtie2_args if bowtie2_args is not None else '',
' --sam-no-qname-trunc --local -t --no-hd --mm -x',
bowtie2_index_base, '--12 -'])
delegate_command = ''.join(
[sys.executable, ' ', os.path.realpath(__file__)[:-3],
('_delegate.py --task-partition {task_partition} '
'--other-reads {other_reads} --second-pass-reads '
'{second_pass_reads} --min-readlet-size '
'{min_readlet_size} {drop_deletions} '
'--max-readlet-size {max_readlet_size} '
'--readlet-interval {readlet_interval} '
'--capping-multiplier {capping_multiplier:1.12f} '
'{verbose} --report-multiplier {report_multiplier:1.12f} '
'--k-value {k_value} '
'--bowtie-idx {bowtie_index_base} '
'--partition-length {bin_size} '
'--manifest {manifest_file} '
'{exon_differentials} {exon_intervals} '
'--gzip-level {gzip_level} '
'--search-filter {search_filter} '
'--index-count {index_count} '
'--tie-margin {tie_margin} '
'{no_realign} '
'{no_polyA} '
'{output_bam_by_chr}').format(
task_partition=task_partition,
other_reads=other_reads_file,
second_pass_reads=second_pass_file,
min_readlet_size=min_readlet_size,
drop_deletions=('--drop-deletions' if drop_deletions
else ''),
max_readlet_size=max_readlet_size,
readlet_interval=readlet_interval,
capping_multiplier=capping_multiplier,
verbose=('--verbose' if verbose else ''),
report_multiplier=report_multiplier,
k_value=k_value,
bowtie_index_base=bowtie_index_base,
bin_size=bin_size,
manifest_file=manifest_file,
exon_differentials=('--exon-differentials'
if exon_differentials else ''),
exon_intervals=('--exon-intervals'
if exon_intervals else ''),
gzip_level=gzip_level,
search_filter=search_filter,
index_count=index_count,
tie_margin=tie_margin,
no_realign=('--no-realign' if no_realign else ''),
no_polyA=('--no-polyA' if no_polyA else ''),
output_bam_by_chr=('--output-bam-by-chr'
if output_bam_by_chr
else '')
)]
)
full_command = ' | '.join([input_command,
bowtie_command, delegate_command])
print >>sys.stderr, \
'Starting first-pass Bowtie 2 with command: ' + full_command
bowtie_process = subprocess.Popen(' '.join(
['set -exo pipefail;', full_command]
),
bufsize=-1, stdout=sys.stdout, stderr=sys.stderr, shell=True,
executable='/bin/bash')
return_code = bowtie_process.wait()
if return_code:
raise RuntimeError('Error occurred while reading first-pass Bowtie 2 '
'output; exitlevel was %d.' % return_code)
os.remove(align_file)
os.remove(other_reads_file)
if not no_realign:
input_command = 'gzip -cd %s' % second_pass_file
bowtie_command = ' '.join([bowtie2_exe,
bowtie2_args if bowtie2_args is not None else '',
' --sam-no-qname-trunc --local -t --no-hd --mm -x',
bowtie2_index_base, '--12 -'])
delegate_command = ''.join(
[sys.executable, ' ', os.path.realpath(__file__)[:-3],
('_delegate.py --task-partition {task_partition} '
'--min-readlet-size {min_readlet_size} '
'{drop_deletions} '
'--max-readlet-size {max_readlet_size} '
'--readlet-interval {readlet_interval} '
'--capping-multiplier {capping_multiplier:012f} '
'{verbose} '
'--report-multiplier {report_multiplier:012f} '
'--k-value {k_value} '
'--bowtie-idx {bowtie_index_base} '
'--partition-length {bin_size} '
'--manifest {manifest_file} '
'{exon_differentials} {exon_intervals} '
'--gzip-level {gzip_level} '
'--search-filter {search_filter} '
'--index-count {index_count} '
'--tie-margin {tie_margin} '
'{output_bam_by_chr}').format(
task_partition=task_partition,
min_readlet_size=min_readlet_size,
drop_deletions=('--drop-deletions'
if drop_deletions else ''),
readlet_interval=readlet_interval,
max_readlet_size=max_readlet_size,
capping_multiplier=capping_multiplier,
verbose=('--verbose' if verbose else ''),
report_multiplier=report_multiplier,
k_value=k_value,
bowtie_index_base=bowtie_index_base,
bin_size=bin_size,
manifest_file=manifest_file,
exon_differentials=('--exon-differentials'
if exon_differentials else ''),
exon_intervals=('--exon-intervals'
if exon_intervals else ''),
gzip_level=gzip_level,
search_filter=search_filter,
index_count=index_count,
tie_margin=tie_margin,
output_bam_by_chr=('--output-bam-by-chr'
if output_bam_by_chr
else '')
)]
)
full_command = ' | '.join([input_command,
bowtie_command, delegate_command])
print >>sys.stderr, \
'Starting second-pass Bowtie 2 with command: ' + full_command
bowtie_process = subprocess.Popen(' '.join(
['set -exo pipefail;', full_command]
),
bufsize=-1, stdout=sys.stdout, stderr=sys.stderr, shell=True,
executable='/bin/bash')
return_code = bowtie_process.wait()
if return_code:
raise RuntimeError('Error occurred while reading second-pass '
'Bowtie 2 output; exitlevel was %d.'
% return_code)
sys.stdout.flush()
if argument == '--':
argv = sys.argv[:i + 1]
in_args = True
args = parser.parse_args(argv[1:])
reversed_complement_translation_table = string.maketrans('ATCG', 'TAGC')
manifest_object = manifest.LabelsAndIndices(
os.path.expandvars(args.manifest))
reference_index = bowtie_index.BowtieIndexReference(
os.path.expandvars(args.bowtie_idx))
alignment_printer = AlignmentPrinter(
manifest_object,
reference_index,
bin_size=args.partition_length,
output_stream=sys.stdout,
exon_ivals=args.exon_intervals,
exon_diffs=args.exon_differentials,
drop_deletions=args.drop_deletions,
output_bam_by_chr=args.output_bam_by_chr,
tie_margin=args.tie_margin)
alignment_count_to_report, seed, non_deterministic \
= bowtie.parsed_bowtie_args(bowtie_args)
input_line_count = 0
output_line_count = 0
start_time = time.time()
for (qname, ), xpartition in xstream(sys.stdin, 1):
counter.add('partitions')
# While labeled multiread, this list may end up simply a uniread
initial_multiread \
def go(input_stream=sys.stdin,
output_stream=sys.stdout,
bowtie2_exe='bowtie2',
bowtie_index_base='genome',
bowtie2_index_base='genome2',
manifest_file='manifest',
bowtie2_args=None,
bin_size=10000,
verbose=False,
exon_differentials=True,
exon_intervals=False,
report_multiplier=1.2,
min_exon_size=8,
search_filter=1,
min_readlet_size=15,
max_readlet_size=25,
readlet_interval=12,
capping_multiplier=1.5,
drop_deletions=False,
gzip_level=3,
scratch=None,
index_count=1,
output_bam_by_chr=False,
tie_margin=0,
no_realign=False,
no_polyA=False):
""" Runs Rail-RNA-align_reads.
A single pass of Bowtie is run to find end-to-end alignments. Unmapped
reads are saved for readletizing to determine introns in sucessive
reduce steps as well as for realignment in a later map step.
Input (read from stdin)
----------------------------
Tab-delimited input tuple columns in a mix of any of the following
three formats:
Format 1 (single-end, 3-column):
1. Nucleotide sequence or its reversed complement, whichever is first
in alphabetical order
2. 1 if sequence was reverse-complemented else 0
3. Name
4. Quality sequence or its reverse, whichever corresponds to field 1
Format 2 (paired, 2 lines, 3 columns each)
(so this is the same as single-end)
1. Nucleotide sequence for mate 1 or its reversed complement,
whichever is first in alphabetical order
2. 1 if sequence was reverse-complemented else 0
3. Name for mate 1
4. Quality sequence for mate 1 or its reverse, whichever corresponds
to field 1
(new line)
1. Nucleotide sequence for mate 2 or its reversed complement,
whichever is first in alphabetical order
2. 1 if sequence was reverse complemented else 0
3. Name for mate 2
4. Quality sequence for mate 2 or its reverse, whichever corresponds
to field 1
Input is partitioned and sorted by field 1, the read sequence.
Hadoop output (written to stdout)
----------------------------
A given RNAME sequence is partitioned into intervals ("bins") of some
user-specified length (see partition.py).
Exonic chunks (aka ECs; three formats, any or all of which may be
emitted):
Format 1 (exon_ival); tab-delimited output tuple columns:
1. Reference name (RNAME in SAM format) + ';' + bin number
2. Sample index
3. EC start (inclusive) on forward strand
4. EC end (exclusive) on forward strand
Format 2 (exon_diff); tab-delimited output tuple columns:
1. Reference name (RNAME in SAM format) + ';' + bin number
2. max(EC start, bin start) (inclusive) on forward strand IFF diff is
positive and EC end (exclusive) on forward strand IFF diff is
negative
3. Sample index
4. '1' if alignment from which diff originates is "unique" according to
--tie-margin criterion; else '0'
5. +1 or -1 * count, the number of instances of a read sequence for
which to print exonic chunks
Note that only unique alignments are currently output as ivals and/or
diffs.
Format 3 (sam); tab-delimited output tuple columns:
Standard SAM output except fields are in different order, and the first
field corresponds to sample label. (Fields are reordered to facilitate
partitioning by sample name/RNAME and sorting by POS.) Each line
corresponds to a spliced alignment. The order of the fields is as
follows.
1. Sample index if outputting BAMs by sample OR
sample-rname index if outputting BAMs by chr
2. (Number string representing RNAME; see BowtieIndexReference
class in bowtie_index for conversion information) OR
'0' if outputting BAMs by chr
3. POS
4. QNAME
5. FLAG
6. MAPQ
7. CIGAR
8. RNEXT
9. PNEXT
10. TLEN
11. SEQ
12. QUAL
... + optional fields
Insertions/deletions (indel_bed)
tab-delimited output tuple columns:
1. 'I' or 'D' insertion or deletion line
2. Number string representing RNAME
3. Start position (Last base before insertion or
first base of deletion)
4. End position (Last base before insertion or last base of deletion
(exclusive))
5. Inserted sequence for insertions or deleted sequence for deletions
6. Sample index
----Next fields are for introns only; they are '\x1c' for indels----
7. '\x1c'
8. '\x1c'
--------------------------------------------------------------------
9. Number of instances of insertion or deletion in sample; this is
always +1 * count before bed_pre combiner/reducer
Read whose primary alignment is not end-to-end
Tab-delimited output tuple columns (unmapped):
1. Transcriptome Bowtie 2 index group number
2. SEQ
3. 1 if SEQ is reverse-complemented, else 0
4. QNAME
5. QUAL
Tab-delimited output tuple columns (readletized):
1. Readlet sequence or its reversed complement, whichever is first in
alphabetical order
2. read sequence ID + ('-' if readlet
sequence is reverse-complemented; else '+') + '\x1e' + displacement
of readlet's 5' end from read's 5' end + '\x1e' + displacement of
readlet's 3' end from read's 3' end (+, for EXACTLY one readlet of
a read sequence, '\x1e' + read sequence + '\x1e' +
(an '\x1f'-separated list A of unique sample labels with read
sequences that match the original read sequence) + '\x1e' +
(an '\x1f'-separated list of unique sample labels B with read
sequences that match the reversed complement of the original read
sequence)) + '\x1e' + (an '\x1f'-separated list of the number of
instances of the read sequence for each respective sample in list
A) + '\x1e' + (an '\x1f'-separated list of the number of instances
of the read sequence's reversed complement for each respective
sample in list B). Here, a read sequence ID takes the form X:Y,
where X is the "mapred_task_partition" environment variable -- a
unique index for a task within a job -- and Y is the index of the
read sequence relative to the beginning of the input stream.
Tab-delimited tuple columns (postponed_sam):
Standard 11+ -column raw SAM output
Single column (unique):
1. A unique read sequence
Two columns, exactly one line (dummy); ensures creation of intron
index:
1. character "-"
2. the word "dummy"
ALL OUTPUT COORDINATES ARE 1-INDEXED.
input_stream: where to find input reads.
output_stream: where to emit exonic chunks and introns.
bowtie2_exe: filename of Bowtie2 executable; include path if not in
$PATH.
bowtie_index_base: the basename of the Bowtie1 index files associated
with the reference.
bowtie2_index_base: the basename of the Bowtie2 index files associated
with the reference.
manifest_file: filename of manifest
bowtie2_args: string containing precisely extra command-line arguments
to pass to first-pass Bowtie2.
bin_size: genome is partitioned in units of bin_size for later load
balancing.
verbose: True iff more informative messages should be written to
stderr.
exon_differentials: True iff EC differentials are to be emitted.
exon_intervals: True iff EC intervals are to be emitted.
report_multiplier: if verbose is True, the line number of an alignment
or read written to stderr increases exponentially with base
report_multiplier.
min_exon_size: minimum exon size searched for in intron_search.py later
in pipeline; used to determine how large a soft clip on one side of
a read is necessary to pass it on to intron search pipeline
search_filter: how large a soft clip on one side of a read is necessary
to pass it on to intron search pipeline
min_readlet_size: "capping" readlets (that is, readlets that terminate
at a given end of the read) are never smaller than this value
max_readlet_size: size of every noncapping readlet
readlet_interval: number of bases separating successive readlets along
the read
capping_multiplier: successive capping readlets on a given end of a
read are increased in size exponentially with base
capping_multiplier
drop_deletions: True iff deletions should be dropped from coverage
vector
gzip_level: compression level to use for temporary files
scratch: scratch directory for storing temporary files or None if
securely created temporary directory
index_count: number of transcriptome Bowtie 2 indexes to which to
assign unmapped reads for later realignment
output_bam_by_chr: True iff final output BAMs will be by chromosome
tie_margin: allowed score difference per 100 bases among ties in
max score. For example, 150 and 144 are tied alignment scores
for a 100-bp read when --tie-margin is 6.
no_realign: True iff job flow does not need more than readlets: this
usually means only a transcript index is being constructed
no_polyA: kill noncapping readlets that are all As and write as
unmapped all reads with polyA prefixes whose suffixes are <
min_exon_size
No return value.
"""
global _input_line_count
# Required length of prefix after poly(A) is trimmed
remaining_seq_size = max(min_exon_size - 1, 1)
polyA_set = frozenset(['A' * i
for i in xrange(1, remaining_seq_size + 1)] +
['T' * i
for i in xrange(1, remaining_seq_size + 1)] + [''])
reference_index = bowtie_index.BowtieIndexReference(bowtie_index_base)
manifest_object = manifest.LabelsAndIndices(manifest_file)
alignment_printer = AlignmentPrinter(manifest_object,
reference_index,
bin_size=bin_size,
output_stream=output_stream,
exon_ivals=exon_intervals,
exon_diffs=exon_differentials,
drop_deletions=drop_deletions,
output_bam_by_chr=output_bam_by_chr,
tie_margin=tie_margin)
# Get task partition to pass to align_reads_delegate.py
try:
task_partition = os.environ['mapred_task_partition']
except KeyError:
# Hadoop 2.x?
try:
task_partition = os.environ['mapreduce_task_partition']
except KeyError:
# A unit test is probably being run
task_partition = '0'
temp_dir = make_temp_dir(scratch)
register_cleanup(tempdel.remove_temporary_directories, [temp_dir])
align_file = os.path.join(temp_dir, 'first_pass_reads.temp.gz')
other_reads_file = os.path.join(temp_dir, 'other_reads.temp.gz')
second_pass_file = os.path.join(temp_dir, 'second_pass_reads.temp.gz')
k_value, _, _ = bowtie.parsed_bowtie_args(bowtie2_args)
nothing_doing = True
with xopen(True, align_file, 'w', gzip_level) as align_stream, \
xopen(True, other_reads_file, 'w', gzip_level) as other_stream:
for seq_number, ((seq, ),
xpartition) in enumerate(xstream(sys.stdin, 1)):
if no_polyA and (seq[:-remaining_seq_size] in polyA_set
or seq[remaining_seq_size:] in polyA_set):
if not no_realign:
'''If a sequence is too short without its poly(A) tail,
make all reads with that sequence unmapped. Technically,
this also kills poly(A)s at 5' ends, but we probably
couldn't align those sequences anyway.'''
reversed_complement_seq = seq[::-1].translate(
_reversed_complement_translation_table)
for is_reversed, name, qual in xpartition:
if is_reversed == '0':
alignment_printer.print_unmapped_read(
name, seq, qual)
else:
alignment_printer.print_unmapped_read(
name, reversed_complement_seq, qual[::-1])
continue
nothing_doing = False
'''Select highest-quality read with alphabetically last qname
for first-pass alignment.'''
best_name, best_mean_qual, best_qual_index, i = None, None, 0, 0
others_to_print = dlist()
for is_reversed, name, qual in xpartition:
_input_line_count += 1
others_to_print.append('\t'.join(
[str(seq_number), is_reversed, name, qual]))
mean_qual = (float(sum([ord(score)
for score in qual])) / len(qual))
if (mean_qual > best_mean_qual
or mean_qual == best_mean_qual and name > best_name):
best_qual_index = i
best_mean_qual = mean_qual
best_name = name
to_align = '\t'.join(
['%s\x1d%s' % (is_reversed, name), seq, qual])
i += 1
assert i >= 1
if i == 1:
print >> other_stream, str(seq_number)
else:
for j, other_to_print in enumerate(others_to_print):
if j != best_qual_index:
print >> other_stream, other_to_print
print >> align_stream, to_align
# Print dummy line
print 'dummy\t-\tdummy'
sys.stdout.flush(
) # this is REALLY important b/c called script will stdout
if nothing_doing:
# No input
sys.exit(0)
input_command = 'gzip -cd %s' % align_file
bowtie_command = ' '.join([
bowtie2_exe, bowtie2_args if bowtie2_args is not None else '',
' --sam-no-qname-trunc --local -t --no-hd --mm -x', bowtie2_index_base,
'--12 -'
])
delegate_command = ''.join([
sys.executable, ' ',
os.path.realpath(__file__)[:-3],
('_delegate.py --task-partition {task_partition} '
'--other-reads {other_reads} --second-pass-reads '
'{second_pass_reads} --min-readlet-size '
'{min_readlet_size} {drop_deletions} '
'--max-readlet-size {max_readlet_size} '
'--readlet-interval {readlet_interval} '
'--capping-multiplier {capping_multiplier:1.12f} '
'{verbose} --report-multiplier {report_multiplier:1.12f} '
'--k-value {k_value} '
'--bowtie-idx {bowtie_index_base} '
'--partition-length {bin_size} '
'--manifest {manifest_file} '
'{exon_differentials} {exon_intervals} '
'--gzip-level {gzip_level} '
'--search-filter {search_filter} '
'--index-count {index_count} '
'--tie-margin {tie_margin} '
'{no_realign} '
'{no_polyA} '
'{output_bam_by_chr}').format(
task_partition=task_partition,
other_reads=other_reads_file,
second_pass_reads=second_pass_file,
min_readlet_size=min_readlet_size,
drop_deletions=('--drop-deletions' if drop_deletions else ''),
max_readlet_size=max_readlet_size,
readlet_interval=readlet_interval,
capping_multiplier=capping_multiplier,
verbose=('--verbose' if verbose else ''),
report_multiplier=report_multiplier,
k_value=k_value,
bowtie_index_base=bowtie_index_base,
bin_size=bin_size,
manifest_file=manifest_file,
exon_differentials=('--exon-differentials'
if exon_differentials else ''),
exon_intervals=('--exon-intervals' if exon_intervals else ''),
gzip_level=gzip_level,
search_filter=search_filter,
index_count=index_count,
tie_margin=tie_margin,
no_realign=('--no-realign' if no_realign else ''),
no_polyA=('--no-polyA' if no_polyA else ''),
output_bam_by_chr=('--output-bam-by-chr'
if output_bam_by_chr else ''))
])
full_command = ' | '.join(
[input_command, bowtie_command, delegate_command])
print >>sys.stderr, \
'Starting first-pass Bowtie 2 with command: ' + full_command
bowtie_process = subprocess.Popen(' '.join(
['set -exo pipefail;', full_command]),
bufsize=-1,
stdout=sys.stdout,
stderr=sys.stderr,
shell=True,
executable='/bin/bash')
return_code = bowtie_process.wait()
if return_code:
raise RuntimeError('Error occurred while reading first-pass Bowtie 2 '
'output; exitlevel was %d.' % return_code)
os.remove(align_file)
os.remove(other_reads_file)
if not no_realign:
input_command = 'gzip -cd %s' % second_pass_file
bowtie_command = ' '.join([
bowtie2_exe, bowtie2_args if bowtie2_args is not None else '',
' --sam-no-qname-trunc --local -t --no-hd --mm -x',
bowtie2_index_base, '--12 -'
])
delegate_command = ''.join([
sys.executable, ' ',
os.path.realpath(__file__)[:-3],
('_delegate.py --task-partition {task_partition} '
'--min-readlet-size {min_readlet_size} '
'{drop_deletions} '
'--max-readlet-size {max_readlet_size} '
'--readlet-interval {readlet_interval} '
'--capping-multiplier {capping_multiplier:012f} '
'{verbose} '
'--report-multiplier {report_multiplier:012f} '
'--k-value {k_value} '
'--bowtie-idx {bowtie_index_base} '
'--partition-length {bin_size} '
'--manifest {manifest_file} '
'{exon_differentials} {exon_intervals} '
'--gzip-level {gzip_level} '
'--search-filter {search_filter} '
'--index-count {index_count} '
'--tie-margin {tie_margin} '
'{output_bam_by_chr}').format(
task_partition=task_partition,
min_readlet_size=min_readlet_size,
drop_deletions=('--drop-deletions' if drop_deletions else ''),
readlet_interval=readlet_interval,
max_readlet_size=max_readlet_size,
capping_multiplier=capping_multiplier,
verbose=('--verbose' if verbose else ''),
report_multiplier=report_multiplier,
k_value=k_value,
bowtie_index_base=bowtie_index_base,
bin_size=bin_size,
manifest_file=manifest_file,
exon_differentials=('--exon-differentials'
if exon_differentials else ''),
exon_intervals=('--exon-intervals' if exon_intervals else ''),
gzip_level=gzip_level,
search_filter=search_filter,
index_count=index_count,
tie_margin=tie_margin,
output_bam_by_chr=('--output-bam-by-chr'
if output_bam_by_chr else ''))
])
full_command = ' | '.join(
[input_command, bowtie_command, delegate_command])
print >>sys.stderr, \
'Starting second-pass Bowtie 2 with command: ' + full_command
bowtie_process = subprocess.Popen(' '.join(
['set -exo pipefail;', full_command]),
bufsize=-1,
stdout=sys.stdout,
stderr=sys.stderr,
shell=True,
executable='/bin/bash')
return_code = bowtie_process.wait()
if return_code:
raise RuntimeError('Error occurred while reading second-pass '
'Bowtie 2 output; exitlevel was %d.' %
return_code)
sys.stdout.flush()
reference_index = bowtie_index.BowtieIndexReference(
os.path.expandvars(args.bowtie_idx)
)
manifest_object = manifest.LabelsAndIndices(
os.path.expandvars(args.manifest)
)
alignment_count_to_report, seed, non_deterministic \
= bowtie.parsed_bowtie_args(bowtie_args)
alignment_printer = AlignmentPrinter(
manifest_object,
reference_index,
output_stream=sys.stdout,
bin_size=args.partition_length,
exon_ivals=args.exon_intervals,
exon_diffs=args.exon_differentials,
drop_deletions=args.drop_deletions,
output_bam_by_chr=args.output_bam_by_chr,
tie_margin=args.tie_margin
)
input_line_count, output_line_count = 0, 0
start_time = time.time()
for (qname,), xpartition in xstream(sys.stdin, 1):
alignments = [(qname,) + alignment for alignment in xpartition]
input_line_count += len(alignments)
junction_counts = [alignment[5].count('N') for alignment in alignments]
min_junction_count = min(junction_counts)
if not min_junction_count:
'''There is at least one alignment that overlaps no junctions; report
args = parser.parse_args(argv[1:])
reversed_complement_translation_table = string.maketrans('ATCG', 'TAGC')
manifest_object = manifest.LabelsAndIndices(
os.path.expandvars(args.manifest)
)
reference_index = bowtie_index.BowtieIndexReference(
os.path.expandvars(args.bowtie_idx)
)
alignment_printer = AlignmentPrinter(
manifest_object,
reference_index,
bin_size=args.partition_length,
output_stream=sys.stdout,
exon_ivals=args.exon_intervals,
exon_diffs=args.exon_differentials,
drop_deletions=args.drop_deletions,
output_bam_by_chr=args.output_bam_by_chr,
tie_margin=args.tie_margin
)
alignment_count_to_report, seed, non_deterministic \
= bowtie.parsed_bowtie_args(bowtie_args)
input_line_count = 0
output_line_count = 0
start_time = time.time()
for (qname,), xpartition in xstream(sys.stdin, 1):
counter.add('partitions')
# While labeled multiread, this list may end up simply a uniread
formed; reference_index.rname_lengths[RNAME] is the length of RNAME.'''
reference_index = bowtie_index.BowtieIndexReference(
os.path.expandvars(args.bowtie_idx)
)
# For mapping sample indices back to original sample labels
manifest_object = manifest.LabelsAndIndices(os.path.expandvars(args.manifest))
# To convert sample-rname index to sample index-rname index tuple
sample_and_rname_indexes = SampleAndRnameIndexes(
manifest_object,
args.output_by_chromosome
)
import time
start_time = time.time()
from alignment_handlers import AlignmentPrinter
alignment_printer = AlignmentPrinter(manifest_object, reference_index,
tie_margin=args.tie_margin)
input_line_count = 0
if args.suppress_bam:
# Just grab stats
if args.output_by_chromosome:
for (index, _), xpartition in xstream(sys.stdin, 2):
sample_index, rname_index = (
sample_and_rname_indexes.sample_and_rname_indexes(index)
)
unique_count, total_count = 0, 0
for record in xpartition:
if not (int(record[2]) & 256):
total_count += 1
try:
# seq is at position 8
if alignment_printer.unique(record, seq_index=8):