nmdp-bioinformatics / dashLinks
Data Standards Hackathon for NGS based typing.
☆14Updated last week
Alternatives and similar repositories for dash
Users that are interested in dash are comparing it to the libraries listed below
Sorting:
- Code for classifying unstructured text to tissue ontology terms using natural language processing and machine learning.☆27Updated last year
- Associations of genomic features, drugs and diseases☆48Updated 3 years ago
- A pipeline that takes clinical notes from EHRs and generate phenotype terms, then generate ranked gene list☆37Updated 2 years ago
- An Open Platform for Harmonisation & Analysis of Sequencing & Phenotype Data☆33Updated 3 years ago
- Repository for documentation to support the IEEE 2791-2020 standard. Please see our home page for communications/publications:☆17Updated last year
- Repository for development of the genomic module of the CDM.☆25Updated 6 years ago
- Analysis examples based on the ISB-CGC hosted TCGA data, using Python and IPython Notebooks.☆54Updated 6 years ago
- GWAS Catalog Ontology and Curation Infrastructure☆26Updated this week
- A phenotype-based tool for variant prioritization in WES and WGS data☆41Updated 3 years ago
- A software toolkit for the interconversion of standard data models for phenotypic data☆15Updated last month
- Finding a scalable alternative to the VCF File for genomics analysis☆14Updated 9 years ago
- Distributed execution of bioinformatics tools on Apache Spark. Apache 2 licensed.☆41Updated 11 months ago
- Community-maintained list of resources that the CI4CC organization and the larger cancer informatics community have found useful or are d…☆22Updated 7 years ago
- Documentation for the MatchmakerExchange APIs☆34Updated 2 years ago
- Generic Interactive Variant Analysis browser☆29Updated 3 years ago
- GA4GH Beacon specification.☆33Updated 3 years ago
- Toil workflows for common genomic pipelines☆33Updated 6 years ago
- Python client for MyVariant.info web services.☆23Updated last year
- ☆26Updated 5 years ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆34Updated 2 months ago
- FAIR Genomes semantic metadata model. The core is a YAML file, which is transformed into all other desired output formats.☆13Updated 3 months ago
- non-redundant, compressed, journalled, file-based storage for biological sequences☆47Updated 3 months ago
- LEGACY repository for SODAR Core, preserved for saving review-related issues. See "sodar-core" for the up-to-date repository.☆15Updated 3 years ago
- ☆15Updated 8 months ago
- MyVariant.info: A BioThings API for human variant annotations☆98Updated 5 months ago
- paplot creates various dynamic and interactive reports for cancer genome analysis.☆26Updated 3 years ago
- simple comparison of snakemake, nextflow and cromwell/wdl☆50Updated 5 years ago
- Repo for downloading and storing OMIM data☆19Updated 9 years ago
- Python client for GA4GH htsget protocol☆15Updated 3 years ago
- JARVIS: a comprehensive deep learning framework to prioritise non-coding variants in whole genomes☆24Updated last year