Description Usage Arguments Value Examples
View source: R/load_variants.R
The function is generally internal, but is exported to help the user in debugging input
1 | load_variants(vcf, file_type = "vcf", reference, sample_name)
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file_type |
vcf or call_stats default is vcf |
reference |
/path/to/reference Path to the reference genome used to call variants. Must be a BSGenome object |
sample_name |
The sample name of the tumor in the vcf file |
variant_file |
/path/to/variant/file |
Data frame with 5 columns: chr, start, end, ref_allele, alt_allele
1 2 3 4 5 6 | # Load variant calls from MuTect2
## Not run:
## End(Not run)
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