Alternatives and similar repositories for openhumansimputer

Users that are interested in openhumansimputer are comparing it to the libraries listed below

• iobio / iobio.viz
  Visualization and charting JS library for streaming genomic data
  ☆19Updated 6 months ago
• refresh-bio / GTC
  GenoTypes Compressor
  ☆15Updated 3 years ago
• WGLab / EHR-Phenolyzer
  A pipeline that takes clinical notes from EHRs and generate phenotype terms, then generate ranked gene list
  ☆37Updated last year
• biobuilds / biobuilds
  Curated collection of open-source bioinformatics tools
  ☆28Updated 6 years ago
• kauwelab / PolyRiskScore
  PRSKB is a website and command-line interface tool for calculating polygenic risk scores using GWA studies from the NHGRI-EBI Catalog.
  ☆29Updated 9 months ago
• quinlan-lab / bedqc
  BED QC tool (in the making)
  ☆16Updated 2 years ago
• phenopolis / phenopolis
  An Open Platform for Harmonisation & Analysis of Sequencing & Phenotype Data
  ☆33Updated 2 years ago
• AlistairNWard / vcfPytools
  vcf file manipulation
  ☆21Updated 9 years ago
• EBISPOT / goci
  GWAS Catalog Ontology and Curation Infrastructure
  ☆26Updated 2 months ago
• iobio / iobio.js
  Client side iobio library for building and executing iobio commands
  ☆10Updated 6 years ago
• NCBI-Hackathons / Network_SNPs
  A framework for network analysis and display of SNPs
  ☆19Updated 8 years ago
• Illumina / happyR
  R tools to interact with hap.py output
  ☆15Updated 5 years ago
• iobio / vcf.iobio.io
  ☆27Updated 2 years ago
• kkdey / aRchaic
  Exploration, clustering, visualization and classification of DNA damage patterns
  ☆19Updated 4 years ago
• solvebio / veppy
  Variant Effect Prediction for Python
  ☆15Updated 8 years ago
• medvedevgroup / varmatch
  robust matching of small variant datasets using flexible scoring schemes
  ☆10Updated 5 years ago
• OpenHumans / gennotes
  GenNotes – public consensus annotation of genetic variants
  ☆11Updated 9 years ago
• NCBI-Hackathons / FlowBio
  A fast, easy way to present complex bioinformatics pipelines to biologists
  ☆11Updated 6 years ago
• RahmanTeam / OpEx
  The OpEx (Optimised Exome) pipeline
  ☆9Updated 6 years ago
• lemieuxl / pyplink
  Python module to read binary Plink files.
  ☆17Updated 11 months ago
• tiagoantao / pygenomics
  A library for next generation genomics in Python 3
  ☆18Updated 7 years ago
• rgcgithub / karyoscan
  Abnormal karyotype detection from whole-exome sequence data
  ☆9Updated 7 years ago
• ncbi / graf
  Genetic Relationship And Fingerprinting
  ☆15Updated 2 years ago
• raphael-group / magi
  A web application from the Raphael Lab for mutation annotation and genome interpretation.
  ☆20Updated 7 years ago
• EliLillyCo / pytest-wdl
  WDL plugin for pytest
  ☆48Updated last year
• sbg / sevenbridges-python
  SevenBridges Python Api bindings
  ☆46Updated 3 months ago
• brentp / geneimpacts
  prioritize effects of variant annotations from VEP, SnpEff, et al.
  ☆34Updated 5 months ago
• biocommons / bioutils
  provides common tools and lookup tables used primarily by the hgvs and uta packages
  ☆22Updated 3 months ago
• nf-cmgg / structural
  A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region exp…
  ☆20Updated 3 months ago
• apierleoni / BioGraPy
  Biological Graphic tool in Python
  ☆34Updated 5 years ago