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addaf

Add Allelic Frequence (AF) for vcf from bcftools.

anacore

Libraries for managing standard file formats and objects from NGS

anacore-utils

Scripts for easily process NGS data from medical centers.

awesome-github-profile-readme

😎 A curated list of awesome Github Profile READMEs 📝

bamclipper

Remove primer sequence from BAM alignments by soft-clipping

bash-logger

A simple bash logger utility

bench_leon

Comparison between Leon and Gzip for fastq compression

bioconda-recipes

Conda recipes for the bioconda channel.

biogrinder

char-al

This is my github profile

christmas_tree

Prints christmas tree in the console.

convert_gzip2leon

Script for compressed gzip into LEON (and inverse)

datatables-flask-serverside

Server-side DataTable with Flask

getbadges

ggsashimi

Command-line tool for the visualization of splicing events across multiple samples

github-actions-for-ci

gitignore

A collection of useful .gitignore templates

hello-github-actions

ifcnv

miscellaneous

Some useful things...

mobidetails

WebApp for DNA variants interpretation

mpa

MoBiDiC Priorization Algorithm

neat

outlyzer

An efficient Variant-Caller to highlight low allele-frequency tumor mutations in a clinical practice

p_adt_r_big_2015

Détection de langage dans un mail ou partie d'un mail

rnasplice

rnasplice is a bioinformatics pipeline for RNA-seq alternative splicing analysis

sarek

Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing

skeeball-3000

somaticcaller

splicelauncher

RNAseq pipeline for alternative splicing junctions