read.snpeff.vcfs: Illustrative function to read multiple VCFs
In jjellis/GenomicVis: Genomic Visualisation Routines
Description
Usage
Arguments
Value
Description
Illustrative function to read multiple VCFs and create an appropriate
input data.frame for snv.heatmap.
Usage
1
read.snpeff.vcfs(vcf.files, genome, sample.names = NULL)
Arguments
vcf.files
vcf.files
genome
genome
sample.names
sample.names
Value
A data.frame suitable as input to snv.heatmap.
jjellis/GenomicVis documentation built on May 19, 2019, 11:39 a.m.
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Description Usage Arguments Value
Description
Illustrative function to read multiple VCFs and create an appropriate
input data.frame for snv.heatmap.
Usage
1 | read.snpeff.vcfs(vcf.files, genome, sample.names = NULL)
|
Arguments
vcf.files |
vcf.files |
genome |
genome |
sample.names |
sample.names |
Value
A data.frame suitable as input to snv.heatmap.
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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