Source code for omics_pipe.modules.intogen

#!/usr/bin/env python

from omics_pipe.parameters.default_parameters import default_parameters
from omics_pipe.utils import *
p = Bunch(default_parameters)

[docs]def intogen(sample, intogen_flag): '''Runs Intogen to rank mutations and implication for cancer phenotype. Follows variant calling. input: .vcf output: variant list citation: Gonzalez-Perez et al. 2013. Intogen mutations identifies cancer drivers across tumor types. Nature Methods 10, 1081-1082. link: http://www.intogen.org/ parameters from parameter file: VCF_FILE: INTOGEN_OPTIONS: INTOGEN_RESULTS: INTOGEN_VERSION: USERNAME: WORKING_DIR: TEMP_DIR: SCHEDULER: VARIANT_RESULTS: ''' #vcf_file = p.SNPIR_RESULTS + "/" +sample + "/final_variants.vcf" spawn_job(jobname = 'intogen', SAMPLE = sample, LOG_PATH = p.LOG_PATH, RESULTS_EMAIL = p.RESULTS_EMAIL, SCHEDULER = p.SCHEDULER, walltime = "240:00:00", queue = p.QUEUE, nodes = 1, ppn = 8, memory = "29gb", script = "/intogen_drmaa.sh", args_list = [p.VCF_FILE, p.INTOGEN_OPTIONS, p.INTOGEN_RESULTS, p.INTOGEN_VERSION, p.USERNAME, p.WORKING_DIR, p.TEMP_DIR, sample, p.SCHEDULER, p.VARIANT_RESULTS]) job_status(jobname = 'intogen', resultspath = p.INTOGEN_RESULTS, SAMPLE = sample, outputfilename = sample + "/variant_genes.tsv", FLAG_PATH = p.FLAG_PATH) return
if __name__ == '__main__': intogen(sample, intogen_flag) sys.exit(0)