Annotate non-coding regulatory vars using our GREEN-DB, prediction scores, conservation and pop AF

Quantitative Genetics Tools for Mapping Trait Variation to Mechanisms, Therapeutics, and Interventions - Webinar Series

Customizable workflows based on snakemake and python for the analysis of NGS data

The analysis repository for the Open Pediatric Brain Tumor Atlas Project

python stuff I use

A curated list of bioinformatics bench-marking papers and resources.

MGI's Analysis Workflows and Pipelines managed by the BGA group.

A bioinformatics software tool for clinical interpretation of genetic variants by the 2015 ACMG-AMP guideline

An iobio app for examining gene variants

Scripts for working with Google Cloud Dataproc service

Code tutorials

A curated list of awesome Bioinformatics libraries and software.

Hidden Markov Models in Python, with scikit-learn like API

Structural Variant Index

Download genomes the easy way.

An interactive heatmap visualization built using D3.js

Module Network Inference software

Creates a target specific exome_full192.coverage.txt file required by MutSig

Materials for 12-day course on analyzing RNA-Seq, ChIP-Seq and variant calling data.

List of computational resources for analyzing microbial sequencing data.

➡️️➡️️⬅️️➡️️ Draw gene maps in ggplot2

Filtering and profiling of next-generational sequencing data using region-specific rules