Alternatives and similar repositories for molgenis-emx2

Users that are interested in molgenis-emx2 are comparing it to the libraries listed below

• biocompute-objects / BCO_Documentation
  Repository for documentation to support the IEEE 2791-2020 standard. Please see our home page for communications/publications:
  ☆17Updated last year
• fairgenomes / fairgenomes-semantic-model
  FAIR Genomes semantic metadata model. The core is a YAML file, which is transformed into all other desired output formats.
  ☆13Updated 7 months ago
• ga4gh-beacon / beacon-v2
  Unified repository for the GA4GH Beacon v2 API standard
  ☆32Updated this week
• ImperialCardioGenetics / frequencyFilter
  Allele frequency filtering for Mendelian variant discovery
  ☆18Updated 8 years ago
• PapenfussLab / PathOS
  PathOS is a clinical application for filtering, analysing and reporting on NGS variants
  ☆29Updated 4 years ago
• broadinstitute / seqr-loading-pipelines
  hail-based pipelines for annotating variant callsets and exporting them to elasticsearch
  ☆23Updated this week
• TheJacksonLaboratory / LIRICAL
  LIkelihood Ratio Interpretation of Clinical AbnormaLities
  ☆29Updated 3 months ago
• mikessh / oncofuse
  Predicting oncogenic potential of gene fusions
  ☆12Updated 9 years ago
• nextflow-io / cwl2nxf
  Import a CWL workflow specification to Nextflow script (experimental)
  ☆27Updated 7 years ago
• NCBI-Hackathons / FlowBio
  A fast, easy way to present complex bioinformatics pipelines to biologists
  ☆11Updated 6 years ago
• jamesware / alleleFrequencyApp
  Allele frequency filter app
  ☆14Updated 3 years ago
• ga4gh / wiki
  a place for GA4GH-related wiki pages
  ☆16Updated 8 years ago
• opencb / iva
  Generic Interactive Variant Analysis browser
  ☆29Updated 3 years ago
• DCGenomics / DangerTrack
  ☆13Updated 8 years ago
• common-workflow-lab / wdl2cwl
  [Experimental] Workflow Definition Language (WDL) to CWL
  ☆28Updated 3 years ago
• PharmGKB / pgkb-ngs-pipeline
  PharmGKB NGS Pipeline
  ☆19Updated 6 years ago
• disq-bio / disq
  A library for manipulating bioinformatics sequencing formats in Apache Spark
  ☆32Updated 3 weeks ago
• molgenis / molgenis
  MOLGENIS - for scientific data: management, exploration, integration and analysis.
  ☆118Updated last month
• decodebiology / geneSCF_inactive
  GeneSCF moved to a dedicated GitHub page, https://github.com/genescf/GeneSCF
  ☆20Updated 4 years ago
• nmdp-bioinformatics / ngs
  Next generation sequencing (NGS/HTS) tools.
  ☆19Updated last year
• bahlolab / exSTRa
  Expanded STR algorithm for Illumina sequencing data
  ☆23Updated 3 years ago
• nilesh-tawari / ChronQC
  Manuscript describing ChronQC is now available online in Bioinformatics
  ☆18Updated 6 years ago
• macarthur-lab / gnomad_browser
  gnomAD browser pre-ASHG 2018
  ☆33Updated 4 years ago
• Yandell-Lab / VVP-pub
  VVP (VAAST Variant Prioritizer) rapidly prioritizes genetic variants
  ☆19Updated 7 years ago
• biobuilds / biobuilds
  Curated collection of open-source bioinformatics tools
  ☆28Updated 6 years ago
• JaneliaSciComp / nextflow-spark
  ☆15Updated 5 months ago
• ccmbioinfo / crg2
  Research pipeline for exploring clinically relevant genomic variants
  ☆16Updated last week
• monarch-initiative / pyphetools
  Python Phenopacket Tools
  ☆15Updated last month
• sbg / sevenbridges-r
  Seven Bridges API Client, CWL Schema, Meta Schema, and SDK Helper in R
  ☆36Updated 3 years ago
• goeckslab / isoseq-browser
  ☆13Updated 8 years ago