openSNP / snpr
The sources of the openSNP website
☆177Updated 3 weeks ago
Alternatives and similar repositories for snpr:
Users that are interested in snpr are comparing it to the libraries listed below
- Easy access to human reference genome sequences☆56Updated 2 years ago
- convert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf☆97Updated 5 years ago
- Reference implementation of the APIs defined in ga4gh-schemas. RETIRED 2018-01-24☆98Updated 7 years ago
- Interactive web-based genome browser.☆227Updated 5 years ago
- Browser for ExAC consortium data☆106Updated 3 years ago
- CloudBioLinux: configure virtual (or real) machines with tools for biological analyses☆257Updated last year
- Models and APIs for Genomic data. RETIRED 2018-01-24☆218Updated 2 years ago
- Identifying Y-chromosome haplogroups in arbitrarily large samples of sequenced or genotyped men☆110Updated 2 months ago
- The Refinery Platform is a data management, analysis and visualization system for bioinformatics and computational biology applications. …☆104Updated 2 years ago
- A project to extract CRISPR information from open genetic data.☆111Updated 5 years ago
- NGS Language Bindings☆119Updated last year
- a lightweight db framework for exploring genetic variation.☆320Updated 4 years ago
- Provides access to complex Bioinformatics software (even BioLinux!) in just one command.☆76Updated 7 years ago
- MyVariant.info: A BioThings API for human variant annotations☆93Updated last week
- Software pipeline for the analysis of CRISPR-Cas9 genome editing outcomes from sequencing data☆135Updated 5 years ago
- Server wrapper that turns command line tools into web services☆61Updated 6 years ago
- web-based analysis tool for rare disease genomics☆187Updated last week
- conda recipes for genomic data☆85Updated 3 years ago
- ncbi-vdb☆91Updated this week
- [Historical] Reproducible Analyses for Bioinformatics☆106Updated 6 years ago
- convert 23andme or Ancestry.com raw genotype calls into VCF format, with dbSNP annotations☆56Updated 5 years ago
- HGVS variant name parsing and generation☆174Updated last year
- Quality control methods for human genomic variants.☆62Updated 2 years ago
- An Open Computational Genomics Analysis platform for big data genomics analysis. OpenCGA is maintained and develop by its parent company …☆170Updated last week
- Smart VCF parser DSL☆82Updated 2 years ago
- A FUSE interface to the NCBI Sequence Read Archive (SRA)☆29Updated 5 years ago
- Docker Images tracking the stable Galaxy releases.☆232Updated 2 months ago
- Real-time tracking of influenza evolution☆88Updated last year
- List of gene lists for genomic analyses.☆219Updated 2 years ago
- Language agnostic RESTful data access to Ensembl data over HTTP☆142Updated 2 months ago