Disclaimer: This post is sponsored by Watershed Omics Bench platform. I have personally tested the platform. The opinions and views expressed in this post are solely those of the author and do not represent the views of my employer
Variant calling is the process of identifying and categorizing genetic variants in sequencing data. It is a critical step in the analysis of whole-genome sequencing (WGS) and whole-exome sequencing (WES) data, as it allows researchers to identify potential disease-causing mutations.