ohsu-comp-bio / g2p-aggregatorLinks
Associations of genomic features, drugs and diseases
☆48Updated 3 years ago
Alternatives and similar repositories for g2p-aggregator
Users that are interested in g2p-aggregator are comparing it to the libraries listed below
Sorting:
- MyVariant.info: A BioThings API for human variant annotations☆96Updated 2 months ago
- An information model for representing variant annotations.☆25Updated this week
- Automated generation of tailored bioinformatics Jupyter Notebooks via a user interface.☆119Updated 6 months ago
- Collect of SO Ontologies☆102Updated 2 months ago
- GA4GH Variation Representation Python Implementation☆61Updated last week
- 3D hotspot mutation proximity analysis tool☆50Updated 2 years ago
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆31Updated 2 weeks ago
- phenotype-based prioritization of candidate genes for human diseases☆65Updated 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
- Library for manipulating genomic variants and predicting their effects☆85Updated last year
- Extensible specification for representing and uniquely identifying biological sequence variation☆94Updated this week
- Code for classifying unstructured text to tissue ontology terms using natural language processing and machine learning.☆27Updated last year
- MyGene.info: A BioThings API for gene annotations☆129Updated 3 months ago
- Python biomart API☆69Updated 2 years ago
- DEPRECATED. This tool has been superseded by https://github.com/griffithlab/pVACtools☆61Updated 6 years ago
- A phenotype-based tool for variant prioritization in WES and WGS data☆40Updated 3 years ago
- ☆69Updated 3 years ago
- Bioinformatics pipeline for selecting patient-specific cancer neoantigen vaccines☆88Updated 2 months ago
- A modular annotation tool for genomic variants☆139Updated this week
- CADD scripts release for offline scoring. For more information about CADD, please visit our website☆88Updated last month
- Clinical interpretation of somatic mutations in cancer☆50Updated 9 months ago
- Explore gnomAD datasets on the web☆85Updated this week
- Search across publicly available datasets to find instances where a drug or cell line of interest has been profiled.☆46Updated 7 years ago
- Project Manager for NGS data analysis☆30Updated 2 months ago
- Central repository for the VICC metakb web application☆15Updated this week
- Framework for integrated analysis and plotting of ChIP/RIP/RNA/*-seq data☆87Updated 5 years ago
- The analysis repository for the Open Pediatric Brain Tumor Atlas Project☆105Updated 2 years ago
- Universal Transcript Archive: comprehensive genome-transcript alignments; multiple transcript sources, versions, and alignment methods; a…☆71Updated last month
- Annotation of VCF variants with functional impact and from databases (executable+library)☆63Updated last week
- Hail helper functions for the gnomAD project and Translational Genomics Group☆97Updated this week