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DeepVariant is an analysis pipeline that uses a deep neural network to call genetic variants from next-generation DNA sequencing data.
Run Windows Applications on Linux as if they are native, Use linux applications to launch files files located in windows vm without needing to install applications on vm. With easy to use configura…
python module to plot beautiful and highly customizable genome browser tracks
ChIP-seq analysis notes from Ming Tang
A bioinformatics software tool for clinical interpretation of genetic variants by the 2015 ACMG-AMP guideline
Bibcure helps in boring tasks by keeping your bibfile up to date and normalized...also allows you to easily download all papers inside your bibtex
Automatic and optimised consensus clustering of one or more heterogeneous datasets
NGS-pipe: next-generation sequencing pipelines for precision oncology
CADD scripts release for offline scoring. For more information about CADD, please visit our website
ClassifyCNV: a tool for clinical annotation of copy-number variants
Clinical interpretation of somatic mutations in cancer
A Program that creates a Spotify playlist from a YouTube Playlist
a peak-calling and differential analysis tool for replicated ChIP-Seq data
detection of duplications and deletions using Python based machine learning techniques
Microsatellite Instability Classification using Multiple Instance Learning
A simple implementation of the circular binary segmentation algorithm in python
Simplify snpEff annotations for interesting cases
Linkage disequlibrium-informed PGT-A (LD-PGTA). A package for detecting genotypic signatures of aneuploidy from extremely low-coverage sequence data.
A generalised significance test for individual communities in networks