MOLGENIS EMX2, the latest version of the MOLGENIS data platform.
☆26Oct 8, 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☆52Oct 2, 2026Updated last week
- The MOLGENIS Software generator tool for creating Dynamic Software Infrastructure used in the Life Sciences☆19Sep 5, 2013Updated 13 years ago
- 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
- Variant Annotation, Segregation and Exclusion for family or cohort based rare-disease sequencing studies.☆12Jun 2, 2022Updated 4 years ago
- A set of tools to annotate VCF files with expression and readcount data☆32Sep 23, 2026Updated 2 weeks ago
- Proton VPN Special Offer - Get 70% off • AdSpecial partner offer. Trusted by over 100 million users worldwide. Tested, Approved and Recommended by Experts.
- 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 pipeline for the identification of Compound Heterozygous Variants☆10Nov 10, 2022Updated 3 years ago
- A webtool for the clinical interpretation of CNVs in rare disease patients☆14Jun 10, 2022Updated 4 years ago
- PAnno is a Pharmacogenomics Annotation tool for clinical genomic testing.☆19Dec 28, 2022Updated 3 years ago
- TAPES : a Tool for Assessment and Prioritisation in Exome Studies☆27Jun 22, 2026Updated 3 months ago
- Curated list of resources for variant prioritization☆16Nov 18, 2025Updated 10 months ago
- Omnipy is a high level Python library for type-driven data wrangling and scalable workflow orchestration (under development)☆27Oct 2, 2026Updated last week
- A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data☆13Sep 29, 2026Updated last week
- Clin.iobio - Workflow and reporting for iobio variant analysis pipeline☆12Oct 7, 2025Updated last year
- Wordpress hosting with auto-scaling - Free Trial Offer • AdFully Managed hosting for WordPress and WooCommerce businesses that need reliable, auto-scalable performance. Cloudways SafeUpdates now available.
- Automated ACMG/AMP classification for human variants associated with congenital hearing loss☆11May 14, 2025Updated last year
- A nextflow pipeline for calling CNVs in probe-enriched sequencing workflows☆14Aug 17, 2026Updated last month
- An R package for Standardized Summary, Annotation, Comparison, and Visualization of CNV, CNVR and ROH☆16Oct 17, 2021Updated 4 years ago
- Official code repository for JAX-CNV☆14Jan 16, 2020Updated 6 years ago
- Framework to benchmark algorithms when detecting germline copy number variations (CNVs) from NGS data☆14Dec 24, 2024Updated last year
- Metadata model and schemas for the EJP virtual platform☆18Aug 29, 2024Updated 2 years ago
- Bacterial typing pipeline for clinical NGS data. Written in NextFlow, Python & Bash.☆16Updated this week
- NiPTUNE. A Python library for NIPT analyses.☆11Nov 22, 2021Updated 4 years ago
- (Deprecated) Ansible roles to configure assorted compontents for an Ubuntu VM or container configured with https://github.com/galaxyproje…☆11Nov 9, 2024Updated last year
- 1-Click AI Models by DigitalOcean Gradient • AdDeploy popular AI models on DigitalOcean Gradient GPU virtual machines with just a single click. Zero configuration with optimized deployments.
- 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
- Natural Language Search and Analysis of High Dimensional Genomic Data☆49Aug 18, 2026Updated last month
- do some exercise☆15Dec 2, 2025Updated 10 months ago
- A tool kit to manage many variant on desktop computer☆13Jan 13, 2026Updated 8 months ago
- Serialize JSON into a canonical format.☆17May 23, 2023Updated 3 years ago
- Plot allele frequencies in VCF files☆11Apr 13, 2026Updated 5 months ago
- PhenoSV: Interpretable phenotype-aware model for the prioritization of genes affected by structural variants.☆18Feb 11, 2025Updated last year
- A project to launch the galaxy docker image easily using ansible☆11Jan 22, 2020Updated 6 years ago
- HemTools: a collection of NGS pipelines and bioinformatic analyses☆75Aug 6, 2026Updated 2 months ago
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- Detection and Visualization of Exon-Level Copy Number Variants in Targeted Next Generation Sequencing Data☆18Nov 26, 2021Updated 4 years ago
- A Mendelian approach to variant effect prediction built in keras☆22Aug 22, 2026Updated last month
- A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region exp…☆28Sep 9, 2026Updated last month
- ☆17Oct 17, 2024Updated last year
- Short reads aligner for NIPT/CNV☆16Oct 10, 2018Updated 8 years ago
- Prioritizing Copy Number Variants (CNV) using Phenotype and Gene Functional Similarity☆18Mar 10, 2022Updated 4 years ago
- Unified repository for the GA4GH Beacon v2 API standard☆35Sep 29, 2026Updated last week