This function calls somatic variants in a pair of tumor-normal matched samples, or just in a tumor sample if no matched sample is not available.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 | call_mutect2(
region = "",
bin_path = "tools/gatk/gatk",
tumor_bam = "",
normal_bam = "",
ref_genome = "",
germ_resource = "",
pon = "",
output_dir = "",
output_name = "",
verbose = FALSE,
orientation = TRUE,
mnps = TRUE
)
|
region |
Region to analyze. Optional |
bin_path |
Path to fastQC executable. Default path tools/gatk/gatk. |
tumor_bam |
Path to tumor bam file. |
normal_bam |
Path to germline bam file. |
ref_genome |
Path to reference genome fasta file. |
germ_resource |
Path to germline resources vcf file. |
pon |
Optional Path to panel of normal. |
output_dir |
Path to the output directory. |
output_name |
OPTIONAL Name for the output. If not given the name of one of the samples will be used. |
verbose |
Enables progress messages. Default False. |
mnps |
Report MNPs in vcf file. |
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