phenopolis / phenopolis_genomics_browser
Python API and React frontend for the Phenopolis Genomics Browser
☆31Updated last year
Alternatives and similar repositories for phenopolis_genomics_browser:
Users that are interested in phenopolis_genomics_browser are comparing it to the libraries listed below
- VarFish: comprehensive DNA variant analysis for diagnostics and research☆47Updated this week
- Python library for extracting HPO encoded phenotypes from text☆29Updated last year
- simple comparison of snakemake, nextflow and cromwell/wdl☆50Updated 4 years ago
- Phenotype driven gene prioritization for HPO☆45Updated 3 years ago
- Clinical interpretation of somatic mutations in cancer☆45Updated 2 months ago
- Associations of genomic features, drugs and diseases☆48Updated 2 years ago
- Pedigree drawing with ease☆23Updated 3 years ago
- Calling star alleles in highly polymorphic pharmacogenes (e.g. CYP450 genes) by leveraging genome graph-based variant detection.☆33Updated 3 weeks ago
- ☆32Updated 3 months ago
- a Medical Genetics Sequence Analysis Pipeline☆82Updated this week
- Public repository for VariantValidator project☆75Updated 2 weeks ago
- Genomes on the Cloud, Mapping & Variant Calling Pipelines☆34Updated 8 years ago
- VEP Plugin to annotate high-impact five prime UTR variants☆26Updated 8 months ago
- Tool suite for HGVS variant descriptions☆40Updated last month
- LIkelihood Ratio Interpretation of Clinical AbnormaLities☆28Updated this week
- GA4GH Variation Representation Python Implementation☆55Updated this week
- ☆28Updated 3 months ago
- Fork of ricopili for development of pipeline for family-based data☆17Updated 2 weeks ago
- A modular annotation tool for genomic variants☆120Updated this week
- PGxPOP☆16Updated 2 years ago
- Data and information about the Polaris study☆53Updated 5 years ago
- Website to analyze conflicting assertions in ClinVar☆18Updated last year
- An information model for representing variant annotations.☆18Updated this week
- CrossMap is a python program to lift over genome coordinates from one genome version to another.☆83Updated 2 months ago
- Call and score variants from WGS/WES of rare disease patients.☆99Updated this week
- Tools to convert Illumina IDAT/BPM/EGT/GTC and Affymetrix CEL/CHP files to VCF☆150Updated 2 months ago
- dbVar☆41Updated 2 years ago
- Code for the in-dev PrediXcan Project☆27Updated 2 years ago
- JARVIS: a comprehensive deep learning framework to prioritise non-coding variants in whole genomes☆23Updated 3 months ago
- Extensible specification for representing and uniquely identifying biological sequence variation☆88Updated 3 weeks ago