Tools (written in C using htslib) for manipulating next-generation sequencing data and support GPU

Expedite large-scale identification of CNVs within predefined genomic regions. Online app available for those with GP2 Tier 2 Access.

Carrier statistic is a statistical framework to prioritize disease-related rare variants by integrating gene expression data

A versatile pairwise aligner for genomic and spliced nucleotide sequences

Runs a combination of tools to generate structural variant calls on short-read whole-genome sequencing data

A DSL for data-driven computational pipelines

Execute Dependent/Independent tasks in a reliable way

Code source (en langage M) du calculateur des impôts sur le revenu et sur la fortune

Principal Component Analysis and Fashion

JDK8 Lambda Samples

Results of the bioinformatics career survey 2008