Annotates variants in MAF with OncoKB annotation.

Scanners for Jar files that may be vulnerable to CVE-2021-44228

FLT3-ITD script based on in-silico extension and clustering

a script to automate demultiplexing on the workstation attached to the nextseq

Methods to integrate data from multiple genome sequencing datasets and form consensus variant calls

Find and annotate ITDs using suffix trees and characterize the exogenous segments within the spacer using heat diffusion.

Synthwave inspired colour theme for VS Code 🌅🕶

A community menagarie of automated variant validations using bcbio and the Common Workflow Language

nim wrapper for htslib for parsing genomics data files

Small class to extract + compress .zip, .gz, .rar archives via browser.

Repository of code for use in the ACGS-Gel Workshop

A fork of MindTouch Core from https://sourceforge.net/projects/dekiwiki/

🐝 Finally, your Github Issues in Slack

CLAMMS is a scalable tool for detecting common and rare copy number variants from whole-exome sequencing data.

GATK Variant Calling Workflow using Galaxy, CWL and Cpipe

Aggregate results from bioinformatics analyses across many samples into a single report.

This repository contains recent announcement or blog post from the Genome in a Bottle Consortium

QC3, a quality control tool designed for DNA sequencing data for raw data, alignment, and variant calling.

List of gene lists for genomic analyses.