View source: R/SomaticCombiner.R
| SomaticCombiner | R Documentation |
To merge two VCFs from different somatic callers.
SomaticCombiner( vcf1, vcf2, sources, GENO = c(GT = 1, DP = 1, AD = 1), id_t = "TUMOR", id_n = "NORMAL", pass_only = FALSE )
vcf1 |
VCF object or vcf file |
vcf2 |
VCF object or vcf file |
sources |
The caller of the VCF files. |
GENO |
The GENO item sources of the mereged VCF. For example c(GT = 1, AD = 2). The vector names are the GENO names and the values are the corresponding index. |
id_t |
The tumor sample ID. |
id_n |
The normal/control sample ID. |
pass_only |
If TRUE, only PASS variants will be merged. |
A merged VCF object
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