Call Somatic/Germline variants using Strelka in parallel This function takes a pair of matched samples or single | multiple germline variants and calls variants on them. To specify the variant calling mode supply the right strelka binary. It is recommended to supply a vcf with indel candidates. This can be generated using MANTA workflow. This function parallelizes the number of jobs that can be run.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 | call_variants_strelka_parallel(
bin_path = "tools/strelka-2.9.10/build/bin/configureStrelkaSomaticWorkflow.py",
bin_path2 = "tools/manta-1.6.0/build/bin/configManta.py",
bam_dir = "",
ref_genome = "",
output_dir = "",
patient_id = "",
germ_pattern = "GL",
verbose = FALSE,
targeted = FALSE,
jobs = 1,
threads = 3,
exec_options = "local"
)
|
bin_path |
REQUIRED Path to strelka binary. Somatic or Germline. |
bam_dir |
REQUIRED Path to directory with BAM files. |
ref_genome |
REQUIRED Path to reference genome. |
output_dir |
OPTIONAL Path to the output directory. |
patient_id |
REQUIRED Patient ID to analyze. Has to be in file names to subselect samples. |
germ_pattern |
REQUIRED Pattern used to identify germline samples. Ex GL |
verbose |
DEFAULT==FALSE Enables progress messages. |
targeted |
OPTIONAL If exome/capture method. Default FALSE |
jobs |
OPTIONAL Number of jobs. Default 1 |
threads |
OPTIONAL Number of threads per job. Default 3 |
exec_options |
OPTIONAL Type of execution. local (Single node) / sge (multiple nodes). Default local. |
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