def main():
# Parse & interpret command line flags.
parser = argparse.ArgumentParser(description='Given paired-end .fastq/.fastq.gz files, map to a genome.',
epilog="Written by Nick Semenkovich <*****@*****.**> for the Gordon Lab at "
"Washington University in St. Louis: https://gordonlab.wustl.edu.",
usage='%(prog)s [options]',
formatter_class=argparse.ArgumentDefaultsHelpFormatter)
parser.add_argument('--input-path', '-i', dest="input_path", metavar='input_dir/', type=str,
help='Input path.', required=True)
parser.add_argument('--output-path', '-o', dest="output_path", metavar='output_dir/', type=str,
help='Output path.', required=True)
parser.add_argument('--genome', '-g', dest="genome", metavar='genome', type=str,
choices=['mm9', 'mm10', 'hg18', 'hg19'], help='Genome to use for bowtie2', required=True)
parser.add_argument('--no-parallel', '-np', dest="no_parallel", default=False, action='store_true',
help='Disable parallel job spawning.')
parser.add_argument("--verbose", "-v", dest="verbose", default=False, action='store_true')
parser.add_argument("--no-log", "-nl", dest="nolog", default=False, action='store_true',
help="Do not create a log file.")
args = parser.parse_args()
output_path = _script_helpers.setup_output_path(args.output_path)
_logshim.startLogger(verbose=args.verbose, noFileLog=args.nolog, outPath=output_path)
paired_end_mapping = find_paired_ends(args.input_path, verbose=args.verbose)
run_bowtie2(paired_end_mapping, args.genome, output_path)
def main():
# Parse & interpret command line flags.
parser = argparse.ArgumentParser(description='Pool multiple .bams together for the same sample.'
'Note: This is *only* necessary if you sequenced the same sample multiple times.',
epilog="Written by Nick Semenkovich <*****@*****.**> for the Gordon Lab at "
"Washington University in St. Louis: https://gordonlab.wustl.edu.",
usage='%(prog)s [options]',
formatter_class=argparse.ArgumentDefaultsHelpFormatter)
parser.add_argument('--input-files', '-i', dest="input_files", metavar='input_dir/', type=str,
help='Input files. (Not just a path!)', required=True, nargs='+')
parser.add_argument('--output-path', '-o', dest="output_path", metavar='output_dir/', type=str,
help='Output path.', required=True)
parser.add_argument("--verbose", "-v", dest="verbose", default=False, action='store_true')
parser.add_argument("--no-log", "-nl", dest="nolog", default=False, action='store_true',
help="Do not create a log file.")
args = parser.parse_args()
output_path = _script_helpers.setup_output_path(args.output_path)
_logshim.startLogger(verbose=args.verbose, noFileLog=args.nolog, outPath=output_path)
merge_and_rmdup(args.input_files, output_path)
def main():
# Parse & interpret command line flags.
parser = argparse.ArgumentParser(description='Run a number of standard peak calling algorithms for ATAC-seq data. '
'Expects de-duplicated, sorted, merged, ChrM-removed data.',
epilog="Written by Nick Semenkovich <*****@*****.**> for the Gordon Lab at "
"Washington University in St. Louis: https://gordonlab.wustl.edu.",
usage='%(prog)s [options]',
formatter_class=argparse.ArgumentDefaultsHelpFormatter)
parser.add_argument('--input-path', '-i', dest="input_path", metavar='input_dir/', type=str,
help='Input path (or a specific .bam file).', required=True)
parser.add_argument('--output-path', '-o', dest="output_path", metavar='output_dir/', type=str,
help='Output path.', required=True)
parser.add_argument('--genome', '-g', dest="genome", metavar='genome', type=str,
choices=['ms', 'mm', 'ce', 'dm'], help='Genome size to pass to MACS.', required=True) # TODO: Consider using mm9/mm10, etc. for uniformity?
parser.add_argument('--no-parallel', '-np', dest="no_parallel", default=False, action='store_true',
help='Disable parallel job spawning.')
parser.add_argument('--skip-bam-indexing', dest="skip_bam_indexing", action='store_true',
help='Skip bam indexing (You must have generated indexes independently for peak callers to work!).', required=False)
parser.add_argument('--skip-macs14', dest="skip_macs14", action='store_true',
help='Skip MACS v1.4 peak calling.', required=False)
parser.add_argument('--skip-macs2', dest="skip_macs2", action='store_true',
help='Skip MACS v2 peak calling.', required=False)
parser.add_argument("--verbose", "-v", dest="verbose", default=False, action='store_true')
parser.add_argument("--no-log", "-nl", dest="nolog", default=False, action='store_true',
help="Do not create a log file.")
args = parser.parse_args()
output_path = _script_helpers.setup_output_path(args.output_path)
log_main = _logshim.startLogger(verbose=args.verbose, noFileLog=args.nolog, outPath=output_path)
input_files = _script_helpers.validate_input_files(args.input_path)
# Generate BAM indexes
if not args.skip_bam_indexing:
generate_index(input_files, output_path, disable_parallel=args.no_parallel)
else:
log_main.warn("Skipping bam index .bai generation as requested.")
log_main.warn("You must have generated these separately, otherwise peak callers will fail.")
if not args.skip_macs14:
# Start with old-school MACS 1.4
run_macs14(input_files, output_path, args.genome, disable_parallel=args.no_parallel)
if not args.skip_macs2:
# Now new MACS 2
# macs2 callpeak --nomodel -t $BAM -n $OUT --nolambda --keep-dup all --slocal 10000
run_macs2(input_files, output_path, args.genome, disable_parallel=args.no_parallel)
def main():
# Parse & interpret command line flags.
parser = argparse.ArgumentParser(description='Given input .bam files, fix matepairs, remove duplicates, blacklist bad'
'regions, and sort the output.',
epilog="Written by Nick Semenkovich <*****@*****.**> for the Gordon Lab at "
"Washington University in St. Louis: http://gordonlab.wustl.edu.",
usage='%(prog)s [options]',
formatter_class=argparse.ArgumentDefaultsHelpFormatter)
parser.add_argument('--input-path', '-i', dest="input_path", metavar='input_dir/', type=str,
help='Input path.', required=True)
parser.add_argument('--output-path', '-o', dest="output_path", metavar='output_dir/', type=str,
help='Output path.', required=True)
parser.add_argument('--genome', '-g', dest="genome", metavar='genome', type=str,
choices=['mm9', 'mm10', 'hg18', 'hg19'], help='Genome to use for blacklisting.', required=True)
parser.add_argument('--no-parallel', '-np', dest="no_parallel", default=False, action='store_true',
help='Disable parallel job spawning.')
parser.add_argument("--verbose", "-v", dest="verbose", default=False, action='store_true')
parser.add_argument("--no-log", "-nl", dest="nolog", default=False, action='store_true',
help="Do not create a log file.")
args = parser.parse_args()
output_path = _script_helpers.setup_output_path(args.output_path)
log_main = _logshim.startLogger(verbose=args.verbose, noFileLog=args.nolog, outPath=output_path)
# Samtools requires a temp directory for sorting /sometimes/.
# This seems to only matter if it exceeds the in-ram limits set by the MAX_MEM parameter.
# Sanity check the /tmp directory has a bit of space.
temppath = tempfile.gettempdir()
s = os.statvfs(temppath)
if ((s.f_bavail * s.f_frsize) / (1024 * 1024)) < 10000: # ~10 G, not for any good reason though
log_main.warn('Temp directory %s doesn\'t have a lot of free space!' % (temppath))
input_files = glob.glob(args.input_path + "/*.bam") # Take ALL of the .bams.
large_filter_fixmate_and_sort(input_files, args.genome, output_path, disable_parallel=args.no_parallel)
rmdup_and_blacklist(input_files, args.genome, output_path, disable_parallel=args.no_parallel)
def main():
# Parse & interpret command line flags.
parser = argparse.ArgumentParser(description='Intelligently merge fastq/fastq.gz files from an Illumina pipeline.'
'Merges all L*_R*_* .fastq.gz files into one per sample.',
epilog="Written by Nick Semenkovich <*****@*****.**> for the Gordon Lab at "
"Washington University in St. Louis: http://gordonlab.wustl.edu.",
usage='%(prog)s [options]',
formatter_class=argparse.ArgumentDefaultsHelpFormatter)
parser.add_argument('--input-path', '-i', dest="input_path", metavar='input_dir/', type=str,
help='Input path.', required=True)
parser.add_argument('--output-path', '-o', dest="output_path", metavar='output_dir/', type=str,
help='Output path.', required=True)
parser.add_argument('--no-parallel', '-np', dest="no_parallel", default=False, action='store_true',
help='Disable parallel job spawning.')
# parser.add_argument('--skip-stats', dest="skip_stats", action='store_true',
# help='Skip statistics generation.', required=False)
parser.add_argument("--verbose", "-v", dest="verbose", default=False, action='store_true')
parser.add_argument("--no-log", "-nl", dest="nolog", default=False, action='store_true',
help="Do not create a log file.")
args = parser.parse_args()
output_path = _script_helpers.setup_output_path(args.output_path)
_logshim.startLogger(verbose=args.verbose, noFileLog=args.nolog, outPath=output_path)
# Our goal is to intelligently merge .fastq/.fastq.gz output from an Illumina run
# The Illumina standard pipeline splits by barcode w/ semi-predictable filenames we can use, e.g.
# IsoA-M1-CD4_S1_L001_I1_001.fastq.gz # index (discard)
# IsoA-M1-CD4_S1_L001_R1_001.fastq.gz # end 1, lane 1
# IsoA-M1-CD4_S1_L001_R2_001.fastq.gz # end 2, lane 2
# IsoA-M1-CD4_S1_L002_I1_001.fastq.gz # index (discard), lane 2
# IsoA-M1-CD4_S1_L002_R1_001.fastq.gz # end 1, lane 2
# ...
# TODO: Move some lower glob code up so we can test these functions
merge_strategy = fastq_map_predict(args.input_path, verbose=args.verbose)
fastq_merge(merge_strategy, args.output_path, disable_parallel=args.no_parallel)
def main():
# Parse & interpret command line flags.
parser = argparse.ArgumentParser(
description=
'Run a number of standard peak calling algorithms for ATAC-seq data. '
'Expects de-duplicated, sorted, merged, ChrM-removed data.',
epilog=
"Written by Nick Semenkovich <*****@*****.**> for the Gordon Lab at "
"Washington University in St. Louis: https://gordonlab.wustl.edu.",
usage='%(prog)s [options]',
formatter_class=argparse.ArgumentDefaultsHelpFormatter)
parser.add_argument('--input-path',
'-i',
dest="input_path",
metavar='input_dir/',
type=str,
help='Input path (or a specific .bam file).',
required=True)
parser.add_argument('--output-path',
'-o',
dest="output_path",
metavar='output_dir/',
type=str,
help='Output path.',
required=True)
parser.add_argument(
'--genome',
'-g',
dest="genome",
metavar='genome',
type=str,
choices=['ms', 'mm', 'ce', 'dm'],
help='Genome size to pass to MACS.',
required=True) # TODO: Consider using mm9/mm10, etc. for uniformity?
parser.add_argument('--no-parallel',
'-np',
dest="no_parallel",
default=False,
action='store_true',
help='Disable parallel job spawning.')
parser.add_argument(
'--skip-bam-indexing',
dest="skip_bam_indexing",
action='store_true',
help=
'Skip bam indexing (You must have generated indexes independently for peak callers to work!).',
required=False)
parser.add_argument('--skip-macs14',
dest="skip_macs14",
action='store_true',
help='Skip MACS v1.4 peak calling.',
required=False)
parser.add_argument('--skip-macs2',
dest="skip_macs2",
action='store_true',
help='Skip MACS v2 peak calling.',
required=False)
parser.add_argument("--verbose",
"-v",
dest="verbose",
default=False,
action='store_true')
parser.add_argument("--no-log",
"-nl",
dest="nolog",
default=False,
action='store_true',
help="Do not create a log file.")
args = parser.parse_args()
output_path = _script_helpers.setup_output_path(args.output_path)
log_main = _logshim.startLogger(verbose=args.verbose,
noFileLog=args.nolog,
outPath=output_path)
input_files = _script_helpers.validate_input_files(args.input_path)
# Generate BAM indexes
if not args.skip_bam_indexing:
generate_index(input_files,
output_path,
disable_parallel=args.no_parallel)
else:
log_main.warn("Skipping bam index .bai generation as requested.")
log_main.warn(
"You must have generated these separately, otherwise peak callers will fail."
)
if not args.skip_macs14:
# Start with old-school MACS 1.4
run_macs14(input_files,
output_path,
args.genome,
disable_parallel=args.no_parallel)
if not args.skip_macs2:
# Now new MACS 2
# macs2 callpeak --nomodel -t $BAM -n $OUT --nolambda --keep-dup all --slocal 10000
run_macs2(input_files,
output_path,
args.genome,
disable_parallel=args.no_parallel)
def main():
# Parse & interpret command line flags.
parser = argparse.ArgumentParser(description='Convert hdf5 tables from bamliquidator format to CSV counts tables '
'for use in R and elsewhere. (Necessary as rhdf5 doesn\'t support our data structure.)',
epilog="Written by Nick Semenkovich <*****@*****.**> for the Gordon Lab at "
"Washington University in St. Louis: http://gordonlab.wustl.edu.",
usage='%(prog)s [options]',
formatter_class=argparse.ArgumentDefaultsHelpFormatter)
parser.add_argument('--input-path', '-i', dest="input_path", metavar='input_dir/', type=str,
help='Input path with .h5 files.',
required=True)
parser.add_argument("--overwrite", dest="overwrite", default=False, action='store_true',
help='Regenerate and overwrite output .tsv files, even if they already exist.')
parser.add_argument('--call-genes', dest="call_genes", default=False, action='store_true',
help='Instead of a .tsv (with positions as keys), make a .annotated.tsv with nearby genes.')
parser.add_argument('--normalized', dest="normalized", default=False, action='store_true',
help='Store the normalized counts (counts/total reads) instead of the raw read counts.')
parser.add_argument('--density', dest="density", default=False, action='store_true',
help='Store the width-normalized density (counts/total reads/region size) instead of the raw read counts.')
parser.add_argument('--sizescaled', dest="sizescaled", default=False, action='store_true',
help='Store the size scaled counts (counts/feature size) instead of the raw read counts.')
# Useful for EdgeR/DESeq2, etc. where every locus/position/gene-name must be unique.
parser.add_argument('--flatten', dest="flatten", default=False, action='store_true',
help='Aggregate identical locus IDs and sum their values. '
'Think carefully before you sum non-normalized values!')
genome_choices = sorted(CONFIG['gffs'].keys())
parser.add_argument('--genome', '-g', dest="genome", metavar='genome', type=str, default=None,
choices=genome_choices, help='Genome to use for annotation, one of: %s' % (', '.join(genome_choices)), required=False)
parser.add_argument("--verbose", "-v", dest="verbose", default=False, action='store_true')
parser.add_argument("--no-log", "-nl", dest="nolog", default=False, action='store_true',
help="Do not create a log file.")
args = parser.parse_args()
if args.call_genes and not args.genome:
parser.error('--genome is when requesting --call_genes')
assert((args.density + args.normalized + args.sizescaled) <= 1)
annotationBedTool = None
if args.call_genes:
genome_gff = CONFIG['gffs'][args.genome]
assert(os.access(genome_gff, os.R_OK))
annotationBedTool = pybedtools.BedTool(genome_gff)
# Output path is input path. This also checks that the path is writeable.
output_path = _script_helpers.setup_output_path(args.input_path)
_logshim.startLogger(verbose=args.verbose, noFileLog=args.nolog, outPath=output_path)
input_files = get_input_files(args.input_path)
parse_h5files(input_files,
annotationBedTool=annotationBedTool,
overwrite=args.overwrite,
flatten=args.flatten,
density=args.density,
normalized=args.normalized,
sizescaled=args.sizescaled)
def main():
# Parse & interpret command line flags.
parser = argparse.ArgumentParser(
description='Given paired-end .fastq/.fastq.gz files, map to a genome.',
epilog=
"Written by Nick Semenkovich <*****@*****.**> for the Gordon Lab at "
"Washington University in St. Louis: https://gordonlab.wustl.edu.",
usage='%(prog)s [options]',
formatter_class=argparse.ArgumentDefaultsHelpFormatter)
parser.add_argument('--input-path',
'-i',
dest="input_path",
metavar='input_dir/',
type=str,
help='Input path.',
required=True)
parser.add_argument('--output-path',
'-o',
dest="output_path",
metavar='output_dir/',
type=str,
help='Output path.',
required=True)
parser.add_argument('--genome',
'-g',
dest="genome",
metavar='genome',
type=str,
choices=['mm9', 'mm10', 'hg18', 'hg19'],
help='Genome to use for bowtie2',
required=True)
parser.add_argument('--no-parallel',
'-np',
dest="no_parallel",
default=False,
action='store_true',
help='Disable parallel job spawning.')
parser.add_argument("--verbose",
"-v",
dest="verbose",
default=False,
action='store_true')
parser.add_argument("--no-log",
"-nl",
dest="nolog",
default=False,
action='store_true',
help="Do not create a log file.")
args = parser.parse_args()
output_path = _script_helpers.setup_output_path(args.output_path)
_logshim.startLogger(verbose=args.verbose,
noFileLog=args.nolog,
outPath=output_path)
paired_end_mapping = find_paired_ends(args.input_path,
verbose=args.verbose)
run_bowtie2(paired_end_mapping, args.genome, output_path)
