OpenHumans / genevieveLinks
Genevieve client: using GenNotes, report ClinVar for individual genomes & add consensus notes
☆10Updated 9 years ago
Alternatives and similar repositories for genevieve
Users that are interested in genevieve are comparing it to the libraries listed below
Sorting:
- GenNotes – public consensus annotation of genetic variants☆11Updated 9 years ago
- What's The Function of these genes?☆22Updated 8 years ago
- Curated collection of open-source bioinformatics tools☆28Updated 6 years ago
- Biological Graphic tool in Python☆34Updated 5 years ago
- Stupid Simple Structural Variant View☆25Updated 9 years ago
- Directly create a bigwig file with signal derived from a sorted and indexed bam file.☆11Updated 8 years ago
- Tool to upload SARS-CoV-2 sequences to BH20 Arvados instance and orchestrate analysis☆13Updated 3 years ago
- An integrated high performance bioinformatics toolkit☆23Updated 6 years ago
- pythonic wrapper for libhts (moved to: https://github.com/quinlan-lab/hts-python)☆49Updated 8 years ago
- ☆15Updated 9 years ago
- ☆43Updated 9 years ago
- Online material and code base for the article Coordinates and Intervals in Graph Based Reference Genomes☆11Updated 8 years ago
- Nanopore desc☆18Updated 9 years ago
- Very very long reads, indeed☆13Updated 8 years ago
- normalize, left-align, trim, validate and clean VCF files☆20Updated 10 years ago
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 6 years ago
- Trigger the Google Genomics Pipeline API with CWL☆11Updated 8 years ago
- EXPERIMENTAL implementation of side graph☆10Updated 10 years ago
- A collection of well-known bioinformatics programs.☆25Updated 10 years ago
- robust matching of small variant datasets using flexible scoring schemes☆11Updated 5 years ago
- Request for comments on interchangeable bioinformatics containers☆39Updated 6 years ago
- reference free variant assembly☆34Updated 2 years ago
- ☆36Updated 5 years ago
- IPython notebooks to teach Genomics and Population Genetics☆21Updated 8 years ago
- Efficient handling of FASTQ files from Python☆51Updated 2 weeks ago
- Provides access to complex Bioinformatics software (even BioLinux!) in just one command.☆76Updated 8 years ago
- ☆12Updated 8 years ago
- SVG based genome viewer written in javascript using D3☆33Updated 10 years ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 6 years ago
- vgraph is a command line application and Python library to compare genetic variants using variant graphs. ``vgraph`` utilizes a graph re…☆43Updated 4 years ago