Dear biostars community, For an analysis, I would like to have the predicted Loss of Function (pLoF) variants for the grch38 human reference. In gnomAD …

I am working on a pharmacogenomics study focusing on the GPCR gene family and analyzing variant sequences in ~700,000 individuals from the [gnomAD v4 exome …

The **Biostar Herald** publishes user submitted links of bioinformatics relevance. It aims to provide a summary of interesting and relevant information you may have missed. …

Are you a researcher or bioinformatician dealing with genetic data? Say hello to OpenCRAVAT! **What is OpenCRAVAT?** OpenCRAVAT is a powerful, open-source platform designed for …

Are you interested in advancing your skills in genomic and population genetics analyses? Join our live online "Manipulation of NGS Data for Genomic and Population …

Dear Biostars, I need to annotate my human exome sequenced dataset with gnomAD v4 so that I am using a relatively up-to-date summated control dataset …

Hi there, I recently tried to use a tool called appreci8, where it integrates 8 different variant calling softwares into a single tools that can …

OakVar is a genomic variant analysis platform. You can * Annotate genomic variants with diverse annotation sources. * Make databases of annotated variants. * Query …

Roakvar is an R package for genomic variant analysis. It is an R wrapper for OakVar, a Python-based genomic variant analysis platform (OakVar is in …

<p>For a while, I've been working with "genomic data integration", and I have been planning on putting together a literature review/some kind of look in …