sample_vcf.annovar: A Format / Sample file for Annotated vcf file basef on...
In hase62/Neoantimon: Neoantimon: A multifunctional R package for identification of tumor-specific neoantigens
sample_vcf.annovar R Documentation
A Format / Sample file for Annotated vcf file basef on Annovar.
Description
A dataset containing the variant information of a patient.
Usage
data(sample_vcf.annovar)
Format
A data frame with 9 rows and variables including "Chr" "Start" "End" "Ref" "Alt" "Func.refGene (exonic, intron, intergenic, ...)" "ExonicFunc.refGene (exonic nonsynonymous, synonymous, insertion, ...)" "AAChange.refGene (e.g., SLCO1C1:NM_001145944:exon7:c.692_693insG:p.L231fs ...)"
hase62/Neoantimon documentation built on Sept. 21, 2023, 4:23 p.m.
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| sample_vcf.annovar | R Documentation |
A Format / Sample file for Annotated vcf file basef on Annovar.
Description
A dataset containing the variant information of a patient.
Usage
data(sample_vcf.annovar)
Format
A data frame with 9 rows and variables including "Chr" "Start" "End" "Ref" "Alt" "Func.refGene (exonic, intron, intergenic, ...)" "ExonicFunc.refGene (exonic nonsynonymous, synonymous, insertion, ...)" "AAChange.refGene (e.g., SLCO1C1:NM_001145944:exon7:c.692_693insG:p.L231fs ...)"
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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