ga4gh / mme-apisLinks
Documentation for the MatchmakerExchange APIs
☆34Updated last year
Alternatives and similar repositories for mme-apis
Users that are interested in mme-apis are comparing it to the libraries listed below
Sorting:
- Scalable RNA-seq analysis☆73Updated 4 years ago
- Library for manipulating genomic variants and predicting their effects☆85Updated last year
- Reference implementation of the APIs defined in ga4gh-schemas. RETIRED 2018-01-24☆99Updated 7 years ago
- conda recipes for genomic data☆84Updated 4 years ago
- Curated collection of open-source bioinformatics tools☆28Updated 6 years ago
- Efficient handling of FASTQ files from Python☆51Updated 2 weeks ago
- Toil workflows for common genomic pipelines☆33Updated 6 years ago
- non-redundant, compressed, journalled, file-based storage for biological sequences☆47Updated last month
- Browser for ExAC consortium data☆106Updated 3 years ago
- http://bam.iobio.io☆47Updated last year
- A collection of well-known bioinformatics programs.☆25Updated 10 years ago
- An Open Platform for Harmonisation & Analysis of Sequencing & Phenotype Data☆33Updated 3 years ago
- Python client for GA4GH htsget protocol☆15Updated 3 years ago
- Associations of genomic features, drugs and diseases☆48Updated 3 years ago
- Dockerised Next Generation Sequencing Pipeline (QC, Align, Calling, Annotation)☆86Updated 8 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated last week
- EpiViz is a scientific information visualization tool for genetic and epigenetic data, used to aid in the exploration and understanding o…☆71Updated 2 years ago
- A pipelining tool to automate and standardise bioinformatics analyses on cluster environments.☆98Updated 2 years ago
- A fast Python library for VCF files leveraging Cython for speed.☆52Updated 7 years ago
- Website to analyze conflicting assertions in ClinVar☆19Updated last year
- [Experimental] Workflow Definition Language (WDL) to CWL☆28Updated 4 years ago
- paplot creates various dynamic and interactive reports for cancer genome analysis.☆25Updated 2 years ago
- python access to UCSC genomes database☆136Updated 5 years ago
- MyVariant.info: A BioThings API for human variant annotations☆96Updated 3 months ago
- Web client for CIViC: Clinical Interpretations of Variants in Cancer☆50Updated 2 years ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆31Updated 3 weeks ago
- Workflow Description Language compiler for the DNAnexus platform☆42Updated 2 years ago
- This repo provides tools to convert ClinVar data into a tab-delimited flat file, and also provides that resulting tab-delimited flat file…☆128Updated 5 years ago
- ☆63Updated 9 years ago
- Flexible Integration of Data with Deep LEarning☆51Updated 2 years ago