def rsem(inputs, outputs):
"""
:params inputs: a tuple of 1 or 2 fastq.gz files, e.g.
('/path/to/rsem_output/homo_sapiens/GSE50599/GSM1224499/SRR968078_1.fastq.gz',
'/path/to/rsem_output/homo_sapiens/GSE50599/GSM1224499/SRR968078_2.fastq.gz')
"""
inputs = [_ for _ in inputs if not _.endswith('.sra2fastq.COMPLETE')]
# this is equivalent to the sample.outdir or GSM dir
outdir = os.path.dirname(inputs[0])
# the names of parameters are the same as that in gen_qsub_script, but
# their values are more or less different, so better keep them separate
fastq_gz_input = gen_fastq_gz_input(inputs)
res = re.search(PATH_RE, outdir)
gse = res.group('GSE')
species = res.group('species')
gsm = res.group('GSM')
reference_name = config['LOCAL_REFERENCE_NAMES'][species]
sample_name = '{outdir}/{gsm}'.format(**locals())
n_jobs = options.j_rsem
flag_file = outputs[-1]
cmd = config['CMD_RSEM'].format(n_jobs=n_jobs,
fastq_gz_input=fastq_gz_input,
reference_name=reference_name,
sample_name=sample_name,
output_dir=outdir)
misc.execute_log_stdout_stderr(cmd,
flag_file=flag_file,
debug=options.debug)
def rsem(inputs, outputs):
"""
:params inputs: a tuple of 1 or 2 fastq.gz files, e.g.
('/path/to/rsem_output/homo_sapiens/GSE50599/GSM1224499/SRR968078_1.fastq.gz',
'/path/to/rsem_output/homo_sapiens/GSE50599/GSM1224499/SRR968078_2.fastq.gz')
"""
inputs = [_ for _ in inputs if not _.endswith('.sra2fastq.COMPLETE')]
# this is equivalent to the sample.outdir or GSM dir
outdir = os.path.dirname(inputs[0])
# the names of parameters are the same as that in gen_qsub_script, but
# their values are more or less different, so better keep them separate
fastq_gz_input = gen_fastq_gz_input(inputs)
res = re.search(PATH_RE, outdir)
gse = res.group('GSE')
species = res.group('species')
gsm = res.group('GSM')
reference_name = config['LOCAL_REFERENCE_NAMES'][species]
sample_name = '{outdir}/{gsm}'.format(**locals())
n_jobs = options.j_rsem
flag_file = outputs[-1]
cmd = config['CMD_RSEM'].format(
n_jobs=n_jobs,
fastq_gz_input=fastq_gz_input,
reference_name=reference_name,
sample_name=sample_name,
output_dir=outdir)
misc.execute_log_stdout_stderr(cmd, flag_file=flag_file, debug=options.debug)
def sra2fastq(inputs, outputs):
"""for meaning of [SED]RR, see
http://www.ncbi.nlm.nih.gov/books/NBK56913/#search.the_entrez_sra_search_response_pa
S =NCBI-SRA, E = EMBL-SRA, D = DDBJ-SRA
SRR: SRA run accession
ERR: ERA run accession
DRR: DRA run accession
"""
sra, _ = inputs # ignore the flag file from previous task
flag_file = outputs[-1]
outdir = os.path.dirname(os.path.dirname(os.path.dirname(sra)))
cmd = config['CMD_FASTQ_DUMP'].format(output_dir=outdir, accession=sra)
misc.execute_log_stdout_stderr(cmd, flag_file=flag_file, debug=options.debug)
def sra2fastq(inputs, outputs):
"""for meaning of [SED]RR, see
http://www.ncbi.nlm.nih.gov/books/NBK56913/#search.the_entrez_sra_search_response_pa
S =NCBI-SRA, E = EMBL-SRA, D = DDBJ-SRA
SRR: SRA run accession
ERR: ERA run accession
DRR: DRA run accession
"""
sra, _ = inputs # ignore the flag file from previous task
flag_file = outputs[-1]
outdir = os.path.dirname(os.path.dirname(os.path.dirname(sra)))
cmd = config['CMD_FASTQ_DUMP'].format(output_dir=outdir, accession=sra)
misc.execute_log_stdout_stderr(cmd,
flag_file=flag_file,
debug=options.debug)
def main():
options = parse_args_for_rp_transfer()
config = misc.get_config(options.config_file)
# r_: means relevant to remote host, l_: to local host
l_top_outdir = config['LOCAL_TOP_OUTDIR']
r_top_outdir = config['REMOTE_TOP_OUTDIR']
G = PPR.gen_all_samples_from_soft_and_isamp
samples = G(options.soft_files, options.isamp, config)
PPR.init_sample_outdirs(samples, l_top_outdir)
r_host, r_username = config['REMOTE_HOST'], config['USERNAME']
fastq2rsem_ratio = config['FASTQ2RSEM_RATIO']
r_cmd_df = config['REMOTE_CMD_DF']
r_min_free = misc.ugly_usage(config['REMOTE_MIN_FREE'])
r_max_usage = misc.ugly_usage(config['REMOTE_MAX_USAGE'])
r_free_to_use = calc_remote_free_space_to_use(
r_host, r_username, r_top_outdir, l_top_outdir,
r_cmd_df, r_max_usage, r_min_free, fastq2rsem_ratio)
# tf: transfer/transferred
tf_record = os.path.join(l_top_outdir, 'transferred_GSMs.txt')
tf_gsms = get_gsms_transferred(tf_record)
tf_gsms_bn = map(os.path.basename, tf_gsms)
logger.info('Selecting samples to transfer based their estimated remote usage')
gsms_to_tf = select_gsms_to_transfer(
samples, tf_gsms_bn, l_top_outdir, r_free_to_use, fastq2rsem_ratio)
if not gsms_to_tf:
logger.info('Cannot find a GSM that fits the current disk usage rule')
return
logger.info('GSMs to transfer:')
for k, gsm in enumerate(gsms_to_tf):
logger.info('\t{0:3d} {1:30s} {2}'.format(k+1, gsm, gsm.outdir))
gsms_to_tf_ids = [os.path.relpath(_.outdir, l_top_outdir)
for _ in gsms_to_tf]
tf_script = write_transfer_sh(
gsms_to_tf_ids, options.rsync_template, l_top_outdir,
r_username, r_host, r_top_outdir)
os.chmod(tf_script, stat.S_IRUSR | stat.S_IWUSR| stat.S_IXUSR)
rcode = misc.execute_log_stdout_stderr(tf_script)
if rcode == 0:
# different from processing in rsempipeline.py, where the completion is
# marked by .COMPLETE flags, but by writting the completed GSMs to
# gsms_transfer_record
append_transfer_record(gsms_to_tf_ids, tf_record)
