OpenHumans / gennotesLinks
GenNotes – public consensus annotation of genetic variants
☆11Updated 9 years ago
Alternatives and similar repositories for gennotes
Users that are interested in gennotes are comparing it to the libraries listed below
Sorting:
- Genevieve client: using GenNotes, report ClinVar for individual genomes & add consensus notes☆10Updated 8 years ago
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- Curated collection of open-source bioinformatics tools☆28Updated 6 years ago
- Client side iobio library for building and executing iobio commands☆10Updated 6 years ago
- Trigger the Google Genomics Pipeline API with CWL☆11Updated 8 years ago
- A web application from the Raphael Lab for mutation annotation and genome interpretation.☆20Updated 7 years ago
- Request for comments on interchangeable bioinformatics containers☆40Updated 5 years ago
- EXPERIMENTAL implementation of side graph☆10Updated 10 years ago
- Benchmarking toolkit for variant calling☆47Updated 4 years ago
- Variant Effect Prediction for Python☆15Updated 8 years ago
- Mostly deprecated in favor of : https://github.com/hbc/bcbioRNASeq. Quality control, differential gene/transcript expression and pathway …☆24Updated 7 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 5 months ago
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 5 years ago
- What's The Function of these genes?☆22Updated 8 years ago
- A library for next generation genomics in Python 3☆18Updated 7 years ago
- ☆12Updated 8 years ago
- SNAPR: a bioinformatics pipeline for efficient and accurate RNA-seq alignment and analysis☆25Updated 10 years ago
- GenoTypes Compressor☆15Updated 3 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆50Updated 5 months ago
- RNF framework for NGS: simulation of reads, evaluation of mappers, conversion of RNF-compliant data.☆14Updated 6 years ago
- [Experimental] Workflow Definition Language (WDL) to CWL☆28Updated 3 years ago
- Railroadtracks is a Python package to handle connected computation steps for DNA and RNA Seq.☆14Updated 9 years ago
- Galaxy Github repository BETA 1. May be destroyed and recreated if post-conversion problems are found (but post-conversion commits on thi…☆12Updated 10 years ago
- ☆37Updated 4 years ago
- Directly create a bigwig file with signal derived from a sorted and indexed bam file.☆11Updated 7 years ago
- Javascript library for visualizing genomics data with D3.☆19Updated 8 years ago
- Biological Graphic tool in Python☆34Updated 5 years ago
- [Bio in Docker] Symposium 2015☆21Updated 7 years ago
- ☆43Updated 9 years ago
- robust matching of small variant datasets using flexible scoring schemes☆10Updated 5 years ago