Alternatives and similar repositories for phenotypeXpression

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

• ccmbioinfo / crg2
  Research pipeline for exploring clinically relevant genomic variants
  ☆16Updated last week
• biodatascience / datasci611
  Materials for Principles of Data Science BIOS 611
  ☆20Updated 5 years ago
• NCBI-Hackathons / FlowBio
  A fast, easy way to present complex bioinformatics pipelines to biologists
  ☆11Updated 7 years ago
• bio-ontology-research-group / phenomenet-vp
  A phenotype-based tool for variant prioritization in WES and WGS data
  ☆38Updated 2 years ago
• Caleydo / vials
  Vials is a Caleydo Web application for visualizing alternative splicing based on mRNAseq data.
  ☆13Updated 7 years ago
• ncbi / magicblast
  ☆36Updated 5 months ago
• MultiQC / test-data
  Test data for MultiQC.
  ☆21Updated 3 weeks ago
• NCBI-Hackathons / VirusDiscoveryProject
  Software, architecture, and data index design for the 2018/2019 Virus Discovery Project
  ☆30Updated 5 years ago
• mskilab-org / gGnome.js
  ☆26Updated 2 years ago
• phenopolis / phenopolis
  An Open Platform for Harmonisation & Analysis of Sequencing & Phenotype Data
  ☆33Updated 3 years ago
• PapenfussLab / PathOS
  PathOS is a clinical application for filtering, analysing and reporting on NGS variants
  ☆29Updated 4 years ago
• kevinblighe / ClinicalGradeDNAseq
  Automated next generation DNA sequencing analysis pipeline suited for clinical tests, with >99.9% sensitivity to Sanger sequencing at rea…
  ☆26Updated 5 years ago
• statgen / verifyBamID
  ☆28Updated 8 years ago
• opencb / iva
  Generic Interactive Variant Analysis browser
  ☆29Updated 3 years ago
• dnil / rhocall
  Call regions of homozygosity and make tentative UPD calls
  ☆12Updated 3 months ago
• DataBiosphere / data-portal
  ☆10Updated this week
• bcgsc / orca
  Genomics Research Container Architecture
  ☆48Updated 6 years ago
• ewels / clusterflow
  A pipelining tool to automate and standardise bioinformatics analyses on cluster environments.
  ☆98Updated 2 years ago
• AstraZeneca-NGS / simple_sv_annotation
  Simplify snpEff annotations for interesting cases
  ☆22Updated 6 years ago
• marcos-diazg / musica
  MuSiCa - Mutational Signatures in Cancer
  ☆23Updated last year
• statgen / gotcloud
  Genomes on the Cloud, Mapping & Variant Calling Pipelines
  ☆35Updated 8 years ago
• nextflow-io / cwl2nxf
  Import a CWL workflow specification to Nextflow script (experimental)
  ☆27Updated 7 years ago
• pasted / clinical_variant_database
  Rails application for storing and parsing clinical exome VCF files. Gene annotations can be retrieved via Biomart integration from Ensemb…
  ☆10Updated 8 years ago
• Genomon-Project / paplot
  paplot creates various dynamic and interactive reports for cancer genome analysis.
  ☆25Updated 2 years ago
• sbg / smart-variant-filtering
  ☆29Updated 4 years ago
• TheJacksonLaboratory / LIRICAL
  LIkelihood Ratio Interpretation of Clinical AbnormaLities
  ☆29Updated 3 months ago
• churchill-lab / g2gtools
  Personal diploid genome creation and coordinate conversion
  ☆30Updated 6 months ago
• gogetdata / ggd-cli
  The command-line interface to GGD
  ☆42Updated 2 years ago
• ncbi / dbvar
  dbVar
  ☆40Updated 3 years ago
• mlin / spVCF
  Sparse Project VCF: evolution of VCF to encode population genotype matrices efficiently
  ☆58Updated last year