combine.vcfs: A function to merge two vcf data frames
In spflanagan/gwscaR: Genome-wide Selection Components Analysis in R
Description
Usage
Arguments
Value
Description
A function to merge two vcf data frames
Usage
1
combine.vcfs(vcf1, vcf2, vcf.name = "merge.vcf")
Arguments
vcf1
A dataframe with genomic data in vcf format
vcf2
A dataframe with genomic data in vcf format
vcf.name
A name for a file with the new vcf file (default is merge.vcf)
Value
A new data.frame in vcf format
spflanagan/gwscaR documentation built on Nov. 14, 2019, 9:16 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.
Description Usage Arguments Value
Description
A function to merge two vcf data frames
Usage
1 | combine.vcfs(vcf1, vcf2, vcf.name = "merge.vcf")
|
Arguments
vcf1 |
A dataframe with genomic data in vcf format |
vcf2 |
A dataframe with genomic data in vcf format |
vcf.name |
A name for a file with the new vcf file (default is merge.vcf) |
Value
A new data.frame in vcf format
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.