View source: R/somenone_gridss.R
| gridss_parse_multi_vcf | R Documentation | 
Parse multi-sample VCF (recommended output of GRIDSS)
gridss_parse_multi_vcf(vcf, germline_id, which_genome = NULL)
| vcf,  | the VCF file path | 
| which_genome,  | genome assembly used ("hg19", "hg38") | 
a list with recurrent SVs and private SVs as elements
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