Entering edit mode
13.2 years ago
jessada
▴
150
I this to create input file in annova generic format from VariBench. In short, in VariBench dataset, they have "mRNA accession", "start position in mRNA", "end position in mRNA", "reference nucleotide" and "missense nucleotide". Are there any ways to parse them? Other than using refGene from
annotate_variation.pl -downdb -buildver hg19 refGene humandb