split_input_haplotypes: Split a single vcf into separate vcfs for each chromosome
In Wedge-lab/battenberg: Battenberg subclonal copy number caller
View source: R/haplotype_external.R
split_input_haplotypes R Documentation
Split a single vcf into separate vcfs for each chromosome
Description
Split a single vcf into separate vcfs for each chromosome
Usage
split_input_haplotypes(chrom_names, externalhaplotypefile = NA, outprefix)
Arguments
chrom_names
Names of the chromosomes
outprefix
Full path and prefix of the output files
externalHaplotypeFile
Full path of the external vcf containing phased haplotypes (Default: NA)
Author(s)
jdemeul
Wedge-lab/battenberg documentation built on July 31, 2023, 1:32 p.m.
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
View source: R/haplotype_external.R
| split_input_haplotypes | R Documentation |
Split a single vcf into separate vcfs for each chromosome
Description
Split a single vcf into separate vcfs for each chromosome
Usage
split_input_haplotypes(chrom_names, externalhaplotypefile = NA, outprefix)
Arguments
chrom_names |
Names of the chromosomes |
outprefix |
Full path and prefix of the output files |
externalHaplotypeFile |
Full path of the external vcf containing phased haplotypes (Default: NA) |
Author(s)
jdemeul
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
Embedding an R snippet on your website
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.