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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