Alternatives and similar repositories for vrs-python

Users that are interested in vrs-python are comparing it to the libraries listed below

• ga4gh / vrs
  Extensible specification for representing and uniquely identifying biological sequence variation
  ☆92Updated last week
• biocommons / uta
  Universal Transcript Archive: comprehensive genome-transcript alignments; multiple transcript sources, versions, and alignment methods; a…
  ☆66Updated 4 months ago
• ga4gh / data-repository-service-schemas
  A repository for the schemas used for the Data Repository Service.
  ☆61Updated last week
• biowdl / tasks
  A collection of reusable WDL tasks. Category:Other
  ☆87Updated last week
• ga4gh / va-spec
  An information model for representing variant annotations.
  ☆21Updated last week
• Clinical-Genomics / genmod
  Annotate models of genetic inheritance patterns in variant files (vcf files)
  ☆82Updated last month
• The-Sequence-Ontology / SO-Ontologies
  Collect of SO Ontologies
  ☆100Updated last week
• SACGF / cdot
  Transcript versions for HGVS libraries
  ☆33Updated last week
• exomiser / Exomiser
  A Tool to Annotate and Prioritize Exome Variants
  ☆222Updated 3 weeks ago
• KarchinLab / open-cravat
  A modular annotation tool for genomic variants
  ☆126Updated 2 weeks ago
• ga4gh / ga4gh-server
  Reference implementation of the APIs defined in ga4gh-schemas. RETIRED 2018-01-24
  ☆98Updated 7 years ago
• stevekm / nextflow-demos
  Example Nextflow pipelines and programming techniques
  ☆107Updated 2 months ago
• Illumina / Nirvana
  The nimble & robust variant annotator
  ☆183Updated last year
• Illumina / interop
  C++ Library to parse Illumina InterOp files
  ☆79Updated last month
• ewels / AWS-iGenomes
  Documentation and description of AWS iGenomes S3 resource.
  ☆114Updated 8 months ago
• 0xTCG / aldy
  Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes
  ☆64Updated this week
• Clinical-Genomics / scout
  VCF visualization interface
  ☆169Updated 2 weeks ago
• dnanexus-rnd / GLnexus
  Scalable gVCF merging and joint variant calling for population sequencing projects
  ☆164Updated last year
• broadinstitute / seqr
  web-based analysis tool for rare disease genomics
  ☆191Updated this week
• macarthur-lab / clinvar
  This repo provides tools to convert ClinVar data into a tab-delimited flat file, and also provides that resulting tab-delimited flat file…
  ☆127Updated 5 years ago
• zwdzwd / transvar
  TransVar - multiway annotator for precision medicine
  ☆126Updated 2 years ago
• KHP-Informatics / ngseasy
  Dockerised Next Generation Sequencing Pipeline (QC, Align, Calling, Annotation)
  ☆86Updated 8 years ago
• sbslee / pypgx
  A Python package for pharmacogenomics (PGx) research
  ☆75Updated 5 months ago
• ga4gh / benchmarking-tools
  Repository for the GA4GH Benchmarking Team work developing standardized benchmarking methods for germline small variant calls
  ☆203Updated 4 years ago
• openvar / variantValidator
  Public repository for VariantValidator project
  ☆76Updated 2 weeks ago
• CCDG / Pipeline-Standardization
  ☆82Updated 6 years ago
• charite / jannovar
  Annotation of VCF variants with functional impact and from databases (executable+library)
  ☆59Updated this week
• nf-core / raredisease
  Call and score variants from WGS/WES of rare disease patients.
  ☆107Updated 3 weeks ago
• konradjk / exac_browser
  Browser for ExAC consortium data
  ☆106Updated 3 years ago
• biothings / myvariant.info
  MyVariant.info: A BioThings API for human variant annotations
  ☆95Updated last week