SnpEff | R Documentation |
Function to make the SnpEff-based vcf readable by extracting the functional annotation and splitting each gene transcript into single rows.
SnpEff(vcf,modifier=F,amino=F,rm_dup=T)
vcf |
SnpEff-based annotated vcf file |
modifier |
if TRUE variants with no impact on gene will be removed |
amino |
if TRUE variants that do not change the amino acid sequence will be removed |
rm_dup |
if TRUE duplicated transcripts for each variant will be removed |
SnpEff(vcf,modifier=F,amino=F,rm_dup=T)
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