ga4gh / vrs-pythonLinks
GA4GH Variation Representation Python Implementation
☆60Updated this week
Alternatives and similar repositories for vrs-python
Users that are interested in vrs-python are comparing it to the libraries listed below
Sorting:
- Extensible specification for representing and uniquely identifying biological sequence variation☆94Updated 2 months ago
- A modular annotation tool for genomic variants☆129Updated last week
- Universal Transcript Archive: comprehensive genome-transcript alignments; multiple transcript sources, versions, and alignment methods; a…☆70Updated last month
- An information model for representing variant annotations.☆22Updated this week
- Collect of SO Ontologies☆101Updated 3 weeks ago
- Annotate models of genetic inheritance patterns in variant files (vcf files)☆84Updated last month
- Annotation of VCF variants with functional impact and from databases (executable+library)☆63Updated last week
- Public repository for VariantValidator project☆77Updated this week
- A repository for the schemas used for the Data Repository Service.☆63Updated 2 months ago
- A collection of reusable WDL tasks. Category:Other☆88Updated last month
- Transcript versions for HGVS libraries☆33Updated this week
- C++ Library to parse Illumina InterOp files☆79Updated 3 months ago
- non-redundant, compressed, journalled, file-based storage for biological sequences☆47Updated last month
- Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes☆64Updated 2 months ago
- CLI for interacting with Cromwell servers☆55Updated last year
- A Python package for pharmacogenomics (PGx) research☆79Updated 7 months ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆29Updated 3 months ago
- Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing☆133Updated 5 years ago
- MyVariant.info: A BioThings API for human variant annotations☆95Updated 3 weeks ago
- Hail helper functions for the gnomAD project and Translational Genomics Group☆96Updated last week
- Browser for ExAC consortium data☆106Updated 3 years ago
- a Medical Genetics Sequence Analysis Pipeline☆84Updated this week
- ☆82Updated 6 years ago
- ☆180Updated 2 years ago
- Workflows for converting between sequence data formats☆39Updated 4 years ago
- A Tool to Annotate and Prioritize Exome Variants☆228Updated last month
- dbVar☆40Updated 3 years ago
- VarSim: A high-fidelity simulation validation framework for high-throughput genome sequencing with cancer applications☆91Updated last year
- Documentation and description of AWS iGenomes S3 resource.☆116Updated 10 months ago
- This repository contains information about latest release from Genome in a Bottle project☆75Updated 6 years ago