MOLGENIS EMX2, the latest version of the MOLGENIS data platform.
☆27Oct 26, 2026Updated this week
Alternatives and similar repositories for molgenis-emx2
Users that are interested in molgenis-emx2 are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Variant Interpretation Pipeline☆52Updated this week
- Simon's Data Club - Reference data for Galaxy servers☆11Oct 19, 2026Updated last week
- FAIR Genomes semantic metadata model. The core is a YAML file, which is transformed into all other desired output formats.☆13Aug 12, 2026Updated 2 months ago
- The MOLGENIS Software generator tool for creating Dynamic Software Infrastructure used in the Life Sciences☆19Sep 5, 2013Updated 13 years ago
- MOLGENIS - for scientific data: management, exploration, integration and analysis.☆122Mar 4, 2026Updated 7 months ago
- Deploy on Railway without the complexity - Free Credits Offer • AdConnect your repo and Railway handles the rest with instant previews. Quickly provision container image services, databases, and storage volumes.
- Managing the progress for the RDA Working Group on Fair Mappings (https://www.rd-alliance.org/groups/fair-mappings-wg/).☆12Aug 5, 2026Updated 2 months ago
- Efficient retrieval, download, and unification of genomic data from leading biodiversity databases☆18Updated this week
- Variant Annotation, Segregation and Exclusion for family or cohort based rare-disease sequencing studies.☆12Jun 2, 2022Updated 4 years ago
- ☆11Aug 29, 2022Updated 4 years ago
- Clinical Variant Annotation Pipeline☆10Apr 21, 2020Updated 6 years ago
- A comprehensive platform for population-scale genomic analyses☆10Apr 20, 2026Updated 6 months ago
- Rails application for storing and parsing clinical exome VCF files. Gene annotations can be retrieved via Biomart integration from Ensemb…☆10May 7, 2017Updated 9 years ago
- A set of tools to annotate VCF files with expression and readcount data☆32Oct 13, 2026Updated 2 weeks ago
- A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data☆13Updated this week
- GPU virtual machines on DigitalOcean Gradient AI • AdGet to production fast with high-performance AMD and NVIDIA GPUs you can spin up in seconds. The definition of operational simplicity.
- TAPES : a Tool for Assessment and Prioritisation in Exome Studies☆27Jun 22, 2026Updated 4 months ago
- Automatic Input Documentation for WDL workflows☆12Sep 5, 2024Updated 2 years ago
- Clin.iobio - Workflow and reporting for iobio variant analysis pipeline☆12Oct 7, 2025Updated last year
- (Deprecated) Ansible roles to configure assorted compontents for an Ubuntu VM or container configured with https://github.com/galaxyproje…☆11Nov 9, 2024Updated last year
- Automated ACMG/AMP classification for human variants associated with congenital hearing loss☆11May 14, 2025Updated last year
- Pathogenicity prediction and prioritization of genetic variants.☆20Sep 21, 2026Updated last month
- A webtool for the clinical interpretation of CNVs in rare disease patients☆14Jun 10, 2022Updated 4 years ago
- fRagmentomics is a standardized and user-friendly R package that integrates fragmentomic feature extraction with fragment-level mutation …☆13Oct 20, 2026Updated last week
- ☆18Jul 13, 2021Updated 5 years ago
- Deploy open-source AI quickly and easily - Special Bonus Offer • AdRunpod Hub is built for open source. One-click deployment and autoscaling endpoints without provisioning your own infrastructure.
- An R package for Standardized Summary, Annotation, Comparison, and Visualization of CNV, CNVR and ROH☆16Oct 17, 2021Updated 5 years ago
- Omnipy is a high level Python library for type-driven data wrangling and scalable workflow orchestration (under development)☆27Oct 22, 2026Updated last week
- Framework to benchmark algorithms when detecting germline copy number variations (CNVs) from NGS data☆14Dec 24, 2024Updated last year
- NiPTUNE. A Python library for NIPT analyses.☆11Nov 22, 2021Updated 4 years ago
- scripts to automatically update ANNOVAR db☆20Nov 17, 2021Updated 4 years ago
- Seave is a web platform that enables genetic variants to be easily filtered and annotated with in silico pathogenicity prediction scores …☆17Aug 9, 2018Updated 8 years ago
- Official code repository for JAX-CNV☆14Jan 16, 2020Updated 6 years ago
- Plot allele frequencies in VCF files☆11Apr 13, 2026Updated 6 months ago
- ☆28Sep 18, 2026Updated last month
- Proton VPN Special Offer - Get 70% off • AdSpecial partner offer. Trusted by over 100 million users worldwide. Tested, Approved and Recommended by Experts.
- Natural Language Search and Analysis of High Dimensional Genomic Data☆49Aug 18, 2026Updated 2 months ago
- A tool kit to manage many variant on desktop computer☆13Jan 13, 2026Updated 9 months ago
- Functional-trained variant effect predictor☆18Aug 27, 2026Updated 2 months ago
- A nextflow pipeline for calling CNVs in probe-enriched sequencing workflows☆14Oct 20, 2026Updated last week
- Library for managing Galaxy plugins - tools, index data, and workflows.☆34Sep 6, 2026Updated last month
- Metabolomics Tools for Galaxy☆22Nov 22, 2016Updated 9 years ago
- A project to launch the galaxy docker image easily using ansible☆11Jan 22, 2020Updated 6 years ago