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systemsgenetics
Generic Java genotype reader / writer, QTL mapping software, Strand alignment toolmolgenis
MOLGENIS - for scientific data: management, exploration, integration and analysis.NIPTeR
R Package for Non Invasive Prenatal Testing (NIPT) analysismolgenis-pipelines
Pipelines for NGS, imputation, gwas, ...vip
Variant Interpretation Pipelinecapice
CoNVaDING
Copy Number Variation Detection In Next-generation sequencing Gene panels was designed for small (single-exon) copy number variation (CNV) detection in high coverage next-generation sequencing (NGS) datamolgenis-legacy
The MOLGENIS Software generator tool for creating Dynamic Software Infrastructure used in the Life Sciencesmolgenis_apps-legacy
MOLGENIS Advanced Application and Computation Framework for the Life SciencesscRNA-seq
cluster-utils
Collection of utilities / helper scripts to make life easier on our HPC clusters.NGS_DNA
NGS DNA best practice pipeline for Illumina sequencing - alignment, variant calling, annotation and QCmolgenis-emx2
MOLGENIS EMX2, the latest version of the MOLGENIS data platform.ngs-utils
Collection of notes and scripts related to NGSvite-plugin-inline
Vite plugin that embeds .js and .css as base85 data1M-cells
This is the repository which contains the code that was used to generate the results and figures of the “Single-cell RNA-sequencing reveals widespread personalized, context-specific gene expression regulation in immune cells” paper (https://doi.org/10.1038/s41467-022-30893-5)molgenis-js-rsql
RSQL javascript tools for transforming, encoding and parsing of strings to RSQL and vice versaansible-pipelines
molgenis-tools-commander
A command line interface for MOLGENISmolgenis-service-armadillo
Armadillo; a DataSHIELD implementation, part of the MOLGENIS suitemolgenis-frontend
Frontend code for MOLGENISmolgenis-r-auth
Discover and authenticate against an OpenID server from RGraph2VR
Visualising / Exploring Linked Data (SPARQL Construct queries) in Virtual Reality.PICALO
eQTL interaction optimization using expectation maximizationvip-inheritance-matcher
annotates VCF samples with denovo and possible compound flags and matching inheritance modesNGS_Automated
molgenis-compute
MOLGENIS Compute is a framework for bioinformatics which enables large scale data and computational workflow management in a distributed execution environment.vip-report-template
Report template for Variant Call Format (VCF) Report generatorvip-decision-tree
Decision tree module for the Variant Interpretation Pipeline (vip)NGS_RNA
gavin-plus
A platform for standardized modular downstream genome analysis.docker
Dockerfiles and docker-compose for MOLGENISontocat
OntoCat - Ontology Common API Tasksvip-report
Report generator for Variant Call Format (VCF) filesgavin
Gene specific calibrations for CADD scores based on ClinVar, ExAC and SnpEffGAP
Genotyping Array Pipelinemolgenis-app-biobank-explorer
Vue application for the biobank explorer; A card detail view on BBMRI biobank - collection datahadoop-pipeline
Implementation of a hadoop (map-reduce) Next-Generation Sequencing pipeline for fast single sample genetic diagnostics.molgenis-r-armadillo
Client to manage shared files in the MOLGENIS Armadillo suite from Rmolgenis-tools-emx-downloader
Stand alone tool to download data in EMX format from molgenis serversasterix
Automated PGx pipelinemolgenis-selenium
Selenium tests for molgenis.molgenis-app-genenetwork
vip-report-api
Report API for Variant Call Format (VCF) Report templatesvip-report-vcf
TypeScript VCF library with support for both reading and writingmolgenis-imputation
Rapid generation of genetic imputation scripts for grid/cluster/local environmentsmolgenis-app-lifecycle
App for the LifeCycle cataloguemolgenis-app-autobetes
molgenis-autobetes servermolgenis-expressions
Library to parse and evaluate simple expressionsmolgenis-ops-helm
Operations Helm charts to deploy build infrastructure on Kubernetesds-tidyverse
pgs_based_sample_mix-up_correction
benchmark-gwas-prio
molgenis-r-client
MOLGENIS R client packagemolgenis-apps-core
Core molgenis user interfacevip-inheritance
molgenis-cargo
Easily run existing MOLGENIS releases on your local machineVaSeBuilder
Validation Set BuilderImputation
molgenis_tools-legacy
Standalone runnable tools compiled into JARs with manual, test, example and sourcesAGCT
Array Genotyping Conversion Toolmolgenis-ui-filter
Filter componentsmolgenis-app-snp-visualization
Application for visualising snp (single-nucleotide polymorphism) data using javascriptvue-pdfium
Vue -> HTML -> Puppeteer PDF rendering servicesc-MetaBrain-consortium
molgenis-tools-cmd-annotators
runnable jar to run the molgenis annotatorsprojects-solve-rd
All things related to maintaining the RD3 databasemethylationnetwork
vcf-io
Variant Call Format (VCF) reader and writer Java librarymolgenis-py-client
A Python client for the MOLGENIS REST APIPGx-pipeline
Farmacogenetics pipelinemolgenis-app-pipeline-dashboard
A MOLGENIS 'Track & Trace' dashboard for analysis pipelinesmolgenis-app-genetics
Repository containing modules and features for interacting with, searching through, and visualising genetic datamolgenis-ops-galaxy
Ansible Galaxy public filesvkgl-consensus
VKGL data sharing of variant classifications consensusgdi-localportal
GDI implementation of Local portal: a Molgenis connected to REMS, with Keycloak and Postgresds-tidyverse-client
tsv-vcf-converter
STEMI-scRNA-seq
single cell experiments in STEMI participantsLove Open Source and this site? Check out how you can help us