Source code for omics_pipe.modules.snpir_variants

#!/usr/bin/env python

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


[docs]def snpir_variants(sample, snpir_variants_flag): '''Calls variants using SNPIR pipeline. input: Aligned.out.sort.bam or accepted_hits.bam output: final_variants.vcf file citation: Piskol, R., et al. (2013). "Reliable Identification of Genomic Variants from RNA-Seq Data." The American Journal of Human Genetics 93(4): 641-651. link: http://lilab.stanford.edu/SNPiR/ parameters from parameters file: VARIANT_RESULTS: TEMP_DIR: SAMTOOLS_VERSION: BWA_VERSION: PICARD_VERSION: GATK_VERSION: BEDTOOLS_VERSION: UCSC_TOOLS_VERSION: GENOME: REPEAT_MASKER: SNPIR_ANNOTATION: RNA_EDIT: DBSNP: MILLS: G1000: WORKING_DIR: BWA_RESULTS: SNPIR_VERSION: SNPIR_CONFIG: SNPIR_DIR: ENCODING: ''' spawn_job(jobname = 'snpir_variants', 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 = 32, memory = "30gb", script = "/snpir_drmaa.sh", args_list = [p.VARIANT_RESULTS, p.TEMP_DIR, p.SAMTOOLS_VERSION, p.BWA_VERSION, p.PICARD_VERSION, p.GATK_VERSION, p.BEDTOOLS_VERSION, p.UCSC_TOOLS_VERSION, p.GENOME, p.REPEAT_MASKER, p.SNPIR_ANNOTATION, p.RNA_EDIT, p.DBSNP, p.MILLS, p.G1000, p.WORKING_DIR, sample, p.BWA_RESULTS, p.SNPIR_VERSION, p.SNPIR_CONFIG, p.SNPIR_DIR, p.ENCODING]) job_status(jobname = 'snpir_variants', resultspath = p.VARIANT_RESULTS, SAMPLE = sample, outputfilename = sample + "/final_variants.vcf", FLAG_PATH = p.FLAG_PATH) return
if __name__ == '__main__': snpir_variants(sample, snpir_variants_flag) sys.exit(0)