VCF Analyzer

VCF Analyzer is a cloud-based workflow for annotating and filtering variants from Whole Exome Sequencing (WES) experiments. The tool accepts raw VCF/gVCF files directly from a variant caller and outputs SNPs, INDELs and affected genes, to be prioritized by BioInfoMiner.

Overall, VCF Analyzer streamlines the data-driven identification of sets of impactful, discriminatory genetic variants. Derived signatures give insights into the molecular networks underlying complex phenotypes and restrain considerably the space of candidate causal variants.