def run_main(config, config_file, fc_dir, work_dir, run_info_yaml):
align_dir = os.path.join(work_dir, "alignments")
run_module = "bcbio.distributed"
fc_name, fc_date, run_info = get_run_info(fc_dir, config, run_info_yaml)
fastq_dir, galaxy_dir, config_dir = _get_full_paths(get_fastq_dir(fc_dir), config, config_file)
config_file = os.path.join(config_dir, os.path.basename(config_file))
dirs = {
"fastq": fastq_dir,
"galaxy": galaxy_dir,
"align": align_dir,
"work": work_dir,
"flowcell": fc_dir,
"config": config_dir,
}
run_parallel = parallel_runner(run_module, dirs, config, config_file)
# process each flowcell lane
run_items = add_multiplex_across_lanes(run_info["details"], dirs["fastq"], fc_name)
lanes = ((info, fc_name, fc_date, dirs, config) for info in run_items)
lane_items = run_parallel("process_lane", lanes)
align_items = run_parallel("process_alignment", lane_items)
# process samples, potentially multiplexed across multiple lanes
samples = organize_samples(align_items, dirs, config_file)
samples = run_parallel("merge_sample", samples)
samples = run_parallel("recalibrate_sample", samples)
samples = parallel_realign_sample(samples, run_parallel)
samples = parallel_variantcall(samples, run_parallel)
samples = run_parallel("detect_sv", samples)
samples = run_parallel("process_sample", samples)
samples = run_parallel("generate_bigwig", samples, {"programs": ["ucsc_bigwig"]})
write_project_summary(samples)
write_metrics(run_info, fc_name, fc_date, dirs)
def run_main(config, config_file, work_dir, parallel,
fc_dir=None, run_info_yaml=None):
"""
Run toplevel analysis, processing a set of input files.
config_file -- Main YAML configuration file with system parameters
fc_dir -- Directory of fastq files to process
run_info_yaml -- YAML configuration file specifying inputs to process
"""
setup_logging(config)
fc_name, fc_date, run_info = get_run_info(fc_dir, config, run_info_yaml)
fastq_dir, galaxy_dir, config_dir = _get_full_paths(get_fastq_dir(fc_dir)
if fc_dir else None,
config, config_file)
config_file = os.path.join(config_dir, os.path.basename(config_file))
dirs = {"fastq": fastq_dir, "galaxy": galaxy_dir,
"work": work_dir, "flowcell": fc_dir, "config": config_dir}
run_parallel = parallel_runner(parallel, dirs, config, config_file)
# process each flowcell lane
run_items = add_multiplex_across_lanes(run_info["details"],
dirs["fastq"], fc_name)
lanes = ((info, fc_name, fc_date, dirs, config) for info in run_items)
lane_items = run_parallel("process_lane", lanes)
pipelines = _pair_lanes_with_pipelines(lane_items)
for pipeline, pipeline_items in pipelines.items():
for xs in pipeline.run(config, config_file, run_parallel, dirs, pipeline_items):
assert len(xs) == 1
upload.from_sample(xs[0])
write_metrics(run_info, fc_name, fc_date, dirs)
def run_main(config, config_file, fc_dir, run_info_yaml):
work_dir = os.getcwd()
align_dir = os.path.join(work_dir, "alignments")
fc_name, fc_date = get_flowcell_info(fc_dir)
run_info = _get_run_info(fc_name, fc_date, config, run_info_yaml)
fastq_dir, galaxy_dir, config_dir = _get_full_paths(get_fastq_dir(fc_dir),
config, config_file)
config_file = os.path.join(config_dir, os.path.basename(config_file))
dirs = {"fastq": fastq_dir, "galaxy": galaxy_dir, "align": align_dir,
"work": work_dir, "flowcell": fc_dir, "config": config_dir}
run_items = add_multiplex_across_lanes(run_info["details"], dirs["fastq"], fc_name)
# process each flowcell lane
lanes = ((info, fc_name, fc_date, dirs, config) for info in run_items)
lane_items = _run_parallel("process_lane", lanes, dirs, config)
_run_parallel("process_alignment", lane_items, dirs, config)
# process samples, potentially multiplexed across multiple lanes
sample_files, sample_fastq, sample_info = \
organize_samples(dirs, fc_name, fc_date, run_items)
samples = ((n, sample_fastq[n], sample_info[n], bam_files, dirs, config, config_file)
for n, bam_files in sample_files)
_run_parallel("process_sample", samples, dirs, config)
write_metrics(run_info, fc_name, fc_date, dirs)
def run_main(config, config_file, fc_dir, work_dir, run_info_yaml):
align_dir = os.path.join(work_dir, "alignments")
run_module = "bcbio.distributed"
fc_name, fc_date, run_info = get_run_info(fc_dir, config, run_info_yaml)
fastq_dir, galaxy_dir, config_dir = _get_full_paths(
get_fastq_dir(fc_dir), config, config_file)
config_file = os.path.join(config_dir, os.path.basename(config_file))
dirs = {
"fastq": fastq_dir,
"galaxy": galaxy_dir,
"align": align_dir,
"work": work_dir,
"flowcell": fc_dir,
"config": config_dir
}
run_parallel = parallel_runner(run_module, dirs, config, config_file)
# process each flowcell lane
run_items = add_multiplex_across_lanes(run_info["details"], dirs["fastq"],
fc_name)
lanes = ((info, fc_name, fc_date, dirs, config) for info in run_items)
lane_items = run_parallel("process_lane", lanes)
align_items = run_parallel("process_alignment", lane_items)
# process samples, potentially multiplexed across multiple lanes
samples = organize_samples(align_items, dirs, config_file)
samples = run_parallel("merge_sample", samples)
samples = run_parallel("recalibrate_sample", samples)
samples = parallel_realign_sample(samples, run_parallel)
samples = parallel_variantcall(samples, run_parallel)
samples = run_parallel("process_sample", samples)
samples = run_parallel("generate_bigwig", samples,
{"programs": ["ucsc_bigwig"]})
write_project_summary(samples)
write_metrics(run_info, fc_name, fc_date, dirs)
def run_main(config,
config_file,
work_dir,
parallel,
fc_dir=None,
run_info_yaml=None):
"""Run toplevel analysis, processing a set of input files.
config_file -- Main YAML configuration file with system parameters
fc_dir -- Directory of fastq files to process
run_info_yaml -- YAML configuration file specifying inputs to process
"""
setup_logging(config)
fc_name, fc_date, run_info = get_run_info(fc_dir, config, run_info_yaml)
fastq_dir, galaxy_dir, config_dir = _get_full_paths(
get_fastq_dir(fc_dir) if fc_dir else None, config, config_file)
config_file = os.path.join(config_dir, os.path.basename(config_file))
dirs = {
"fastq": fastq_dir,
"galaxy": galaxy_dir,
"work": work_dir,
"flowcell": fc_dir,
"config": config_dir
}
config = _set_resources(parallel, config)
run_parallel = parallel_runner(parallel, dirs, config, config_file)
# process each flowcell lane
run_items = add_multiplex_across_lanes(run_info["details"], dirs["fastq"],
fc_name)
lanes = ((info, fc_name, fc_date, dirs, config) for info in run_items)
lane_items = run_parallel("process_lane", lanes)
align_items = run_parallel("process_alignment", lane_items)
# process samples, potentially multiplexed across multiple lanes
samples = organize_samples(align_items, dirs, config_file)
samples = run_parallel("merge_sample", samples)
samples = run_parallel("prep_recal", samples)
samples = recalibrate.parallel_write_recal_bam(samples, run_parallel)
samples = parallel_realign_sample(samples, run_parallel)
samples = parallel_variantcall(samples, run_parallel)
samples = run_parallel("postprocess_variants", samples)
samples = combine_multiple_callers(samples)
samples = run_parallel("detect_sv", samples)
samples = run_parallel("combine_calls", samples)
run_parallel("process_sample", samples)
run_parallel("generate_bigwig", samples, {"programs": ["ucsc_bigwig"]})
write_project_summary(samples)
write_metrics(run_info, fc_name, fc_date, dirs)
def run_main(config,
config_file,
work_dir,
parallel,
fc_dir=None,
run_info_yaml=None):
"""
Run toplevel analysis, processing a set of input files.
config_file -- Main YAML configuration file with system parameters
fc_dir -- Directory of fastq files to process
run_info_yaml -- YAML configuration file specifying inputs to process
"""
setup_logging(config)
fc_name, fc_date, run_info = get_run_info(fc_dir, config, run_info_yaml)
fastq_dir, galaxy_dir, config_dir = _get_full_paths(
get_fastq_dir(fc_dir) if fc_dir else None, config, config_file)
config_file = os.path.join(config_dir, os.path.basename(config_file))
dirs = {
"fastq": fastq_dir,
"galaxy": galaxy_dir,
"work": work_dir,
"flowcell": fc_dir,
"config": config_dir
}
run_parallel = parallel_runner(parallel, dirs, config, config_file)
# process each flowcell lane
run_items = add_multiplex_across_lanes(run_info["details"], dirs["fastq"],
fc_name)
lanes = ((info, fc_name, fc_date, dirs, config) for info in run_items)
lane_items = lane.process_all_lanes(lanes, run_parallel)
pipelines = _pair_lanes_with_pipelines(lane_items)
for pipeline, pipeline_items in pipelines.items():
pipeline_items = _add_provenance(pipeline_items, dirs, config)
for xs in pipeline.run(config, config_file, run_parallel, dirs,
pipeline_items):
assert len(xs) == 1
upload.from_sample(xs[0])
qcsummary.write_metrics(run_info, fc_name, fc_date, dirs)
def run_main(config, config_file, work_dir, parallel,
fc_dir=None, run_info_yaml=None):
"""Run toplevel analysis, processing a set of input files.
config_file -- Main YAML configuration file with system parameters
fc_dir -- Directory of fastq files to process
run_info_yaml -- YAML configuration file specifying inputs to process
"""
setup_logging(config)
fc_name, fc_date, run_info = get_run_info(fc_dir, config, run_info_yaml)
fastq_dir, galaxy_dir, config_dir = _get_full_paths(get_fastq_dir(fc_dir) if fc_dir else None,
config, config_file)
config_file = os.path.join(config_dir, os.path.basename(config_file))
dirs = {"fastq": fastq_dir, "galaxy": galaxy_dir,
"work": work_dir, "flowcell": fc_dir, "config": config_dir}
config = _set_resources(parallel, config)
run_parallel = parallel_runner(parallel, dirs, config, config_file)
# process each flowcell lane
run_items = add_multiplex_across_lanes(run_info["details"], dirs["fastq"], fc_name)
lanes = ((info, fc_name, fc_date, dirs, config) for info in run_items)
lane_items = run_parallel("process_lane", lanes)
align_items = run_parallel("process_alignment", lane_items)
# process samples, potentially multiplexed across multiple lanes
samples = organize_samples(align_items, dirs, config_file)
samples = run_parallel("merge_sample", samples)
samples = run_parallel("prep_recal", samples)
samples = recalibrate.parallel_write_recal_bam(samples, run_parallel)
samples = parallel_realign_sample(samples, run_parallel)
samples = parallel_variantcall(samples, run_parallel)
samples = run_parallel("postprocess_variants", samples)
samples = combine_multiple_callers(samples)
samples = run_parallel("detect_sv", samples)
samples = run_parallel("combine_calls", samples)
run_parallel("process_sample", samples)
run_parallel("generate_bigwig", samples, {"programs": ["ucsc_bigwig"]})
write_project_summary(samples)
write_metrics(run_info, fc_name, fc_date, dirs)
def run_main(config, config_file, fc_dir, work_dir, run_info_yaml):
_record_sw_versions(config, os.path.join(work_dir, "bcbb_software_versions.txt"))
prog = utils.RecordProgress(work_dir)
to_compress = set()
prog.progress("analysis_start")
align_dir = os.path.join(work_dir, "alignments")
run_module = "bcbio.distributed"
fc_name, fc_date, run_info = get_run_info(fc_dir, config, run_info_yaml)
fastq_dir, galaxy_dir, config_dir = _get_full_paths(get_fastq_dir(fc_dir),
config, config_file)
config_file = os.path.join(config_dir, os.path.basename(config_file))
dirs = {"fastq": fastq_dir, "galaxy": galaxy_dir, "align": align_dir,
"work": work_dir, "flowcell": fc_dir, "config": config_dir}
run_parallel = parallel_runner(run_module, dirs, config, config_file)
run_items = add_multiplex_across_lanes(run_info["details"], dirs["fastq"], fc_name)
lanes = ((info, fc_name, fc_date, dirs, config) for info in run_items)
lane_items = run_parallel("process_lane", lanes)
[to_compress.add(f) for f in lane_items[0][0:2]]
prog.progress("process_lane")
# upload the sequencing report to Google Docs
# will skip this for now and rely on external mechanism for uploading this data
#gdocs_indicator = os.path.join(work_dir, "gdocs_report_complete.txt")
#if not os.path.exists(gdocs_indicator) \
#and queue_report(fc_date, fc_name, os.path.abspath(run_info_yaml), dirs, config, config_file):
# utils.touch_file(gdocs_indicator)
# Remove spiked in controls, contaminants etc.
lane_items = run_parallel("remove_contaminants", lane_items)
[to_compress.add(f) for f in lane_items[0][0:2]]
prog.progress("remove_contaminants")
align_items = run_parallel("process_alignment", lane_items)
[to_compress.add(f) for f in align_items[0]['fastq']]
prog.progress("process_alignment")
# process samples, potentially multiplexed across multiple lanes
samples = organize_samples(align_items, dirs, config_file)
samples = run_parallel("merge_sample", samples)
to_compress.add(samples[0][0]['fastq1'])
to_compress.add(samples[0][0]['fastq2'])
prog.progress("merge_sample")
samples = run_parallel("mark_duplicates_sample", samples)
to_compress.add(samples[0][0]['fastq1'])
to_compress.add(samples[0][0]['fastq2'])
prog.progress("mark_duplicates_sample")
run_parallel("screen_sample_contaminants", samples)
prog.progress("screen_sample_contaminants")
samples = run_parallel("recalibrate_sample", samples)
prog.progress("recalibrate_sample")
samples = parallel_realign_sample(samples, run_parallel)
prog.progress("realign_sample")
samples = parallel_variantcall(samples, run_parallel)
prog.progress("variantcall")
samples = run_parallel("detect_sv", samples)
prog.progress("detect_sv")
samples = run_parallel("process_sample", samples)
prog.progress("process_sample")
samples = run_parallel("generate_bigwig", samples, {"programs": ["ucsc_bigwig"]})
prog.progress("generate_bigwig")
write_project_summary(samples)
write_metrics(run_info, fc_name, fc_date, dirs)
prog.progress("write_metrics")
# Write statusdb metrics
# will skip this for now and rely on external mechanism for uploading this data
#report_to_statusdb(fc_name, fc_date, run_info_yaml, dirs, config)
#Compress all files in to_compress
if config['algorithm'].get('compress_files', True):
(before, after) = utils.compress_files(to_compress)
logger.info("Space used by the files before compressing (in bytes): " \
+ str(before))
logger.info("Space used by the files after compressing (in bytes): " \
+ str(after))
logger.info("Saved space (in bytes): " + str(before - after))
def run_main(config, config_file, fc_dir, work_dir, run_info_yaml):
_record_sw_versions(config, os.path.join(work_dir, "bcbb_software_versions.txt"))
prog = RecordProgress(work_dir)
to_compress = set()
prog.progress("analysis_start")
align_dir = os.path.join(work_dir, "alignments")
run_module = "bcbio.distributed"
fc_name, fc_date, run_info = get_run_info(fc_dir, config, run_info_yaml)
fastq_dir, galaxy_dir, config_dir = _get_full_paths(get_fastq_dir(fc_dir),
config, config_file)
config_file = os.path.join(config_dir, os.path.basename(config_file))
dirs = {"fastq": fastq_dir, "galaxy": galaxy_dir, "align": align_dir,
"work": work_dir, "flowcell": fc_dir, "config": config_dir}
run_parallel = parallel_runner(run_module, dirs, config, config_file)
run_items = add_multiplex_across_lanes(run_info["details"], dirs["fastq"], fc_name)
lanes = ((info, fc_name, fc_date, dirs, config) for info in run_items)
lane_items = run_parallel("process_lane", lanes)
_add_to_compress(to_compress, lane_items, 'lane_items')
prog.dummy()
prog.progress("process_lane")
# Remove spiked in controls, contaminants etc.
lane_items = run_parallel("remove_contaminants", lane_items)
_add_to_compress(to_compress, lane_items, 'lane_items')
prog.dummy()
prog.progress("remove_contaminants")
align_items = run_parallel("process_alignment", lane_items)
_add_to_compress(to_compress, align_items, 'align_items')
prog.dummy()
prog.progress("process_alignment")
# process samples, potentially multiplexed across multiple lanes
samples = organize_samples(align_items, dirs, config_file)
samples = run_parallel("merge_sample", samples)
_add_to_compress(to_compress, samples, 'samples')
prog.dummy()
prog.progress("merge_sample")
samples = run_parallel("mark_duplicates_sample", samples)
_add_to_compress(to_compress, samples, 'samples')
prog.dummy()
prog.progress("mark_duplicates_sample")
run_parallel("screen_sample_contaminants", samples)
prog.dummy()
prog.progress("screen_sample_contaminants")
samples = run_parallel("recalibrate_sample", samples)
_add_to_compress(to_compress, samples, 'samples')
prog.dummy()
prog.progress("recalibrate_sample")
samples = parallel_realign_sample(samples, run_parallel)
_add_to_compress(to_compress, samples, 'samples')
prog.dummy()
prog.progress("realign_sample")
samples = parallel_variantcall(samples, run_parallel)
_add_to_compress(to_compress, samples, 'samples')
prog.dummy()
prog.progress("variantcall")
samples = run_parallel("detect_sv", samples)
_add_to_compress(to_compress, samples, 'samples')
prog.dummy()
prog.progress("detect_sv")
samples = run_parallel("process_sample", samples)
_add_to_compress(to_compress, samples, 'samples')
prog.dummy()
prog.progress("process_sample")
samples = run_parallel("generate_bigwig", samples, {"programs": ["ucsc_bigwig"]})
_add_to_compress(to_compress, samples, 'samples')
prog.dummy()
prog.progress("generate_bigwig")
write_project_summary(samples)
write_metrics(run_info, fc_name, fc_date, dirs)
prog.dummy()
prog.progress("write_metrics")
# Compress all files in to_compress
if config['algorithm'].get('compress_files', True):
sizes = run_parallel("compress_files", [[[cf]] for cf in to_compress])
before = sum([s[0] for s in sizes])
after = sum([s[1] for s in sizes])
logger.info("Space used by the files before compressing (in bytes): " \
+ str(before))
logger.info("Space used by the files after compressing (in bytes): " \
+ str(after))
logger.info("Saved space (in bytes): " + str(before - after))