split_input_haplotypes: Split a single vcf into separate vcfs for each chromosome
In Wedge-Oxford/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-Oxford/battenberg documentation built on Aug. 4, 2023, 6:27 p.m.
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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.
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