MOLGENIS - open source solutions for scientific data's Projects
Converts Managed Variant Lists to VCF (Variant Call Format) files
Collection of notes and scripts related to NGS
CNV calling pipelines based on NGS data
NGS DNA best practice pipeline for Illumina sequencing - alignment, variant calling, annotation and QC
R Package for Non Invasive Prenatal Testing (NIPT) analysis
OntoCat - Ontology Common API Tasks
General repository to contain ontologies
Farmacogenetics pipeline
eQTL interaction optimization using expectation maximization
All things related to maintaining the RD3 database
The rare diseases data model for Molgenis
RD registry with Molgenis
R package to access S3 compatible object stores as resources
Simple, modern and flexible status page
single cell experiments in STEMI participants
Generic Java genotype reader / writer, QTL mapping software, Strand alignment tool