i just wanted to filter out my variants based on true positive and false positive. i have a separate data of true positive one . now i want to filter out my variants.@DevonRyan
I'm new to NGS data analysis, can anyone suggest me free tools for prioritizing my Variants from the Whole-exome sequencing VCF file. I have annotated …
Hi everybody, I would like to phase (just phasing, not imputation) vcf file containing about 1100 individuals (a given human population) derived from whole genome …
An SVM-based tool for filtering VCF files? What exactly are you trying to accomplish?
@Devon Ryan Yes that what i need
i just wanted to filter out my variants based on true positive and false positive. i have a separate data of true positive one . now i want to filter out my variants.@DevonRyan