AndersenLab / IBiS-BootcampLinks
☆40Updated 8 years ago
Alternatives and similar repositories for IBiS-Bootcamp
Users that are interested in IBiS-Bootcamp are comparing it to the libraries listed below
Sorting:
- Library for indexing VCF files for random access searches by rsID☆17Updated 2 weeks ago
- A fast, easy way to present complex bioinformatics pipelines to biologists☆11Updated 6 years ago
- Trigger the Google Genomics Pipeline API with CWL☆11Updated 8 years ago
- qtools has helper functions to submit jobs to compute clusters (PBS on TSCC, SGE on oolite) from within Python☆21Updated last year
- Bioinformatics pipelines for Resolwe☆17Updated this week
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 8 months ago
- Snakemake skeleton - Build workflows with Snakemake☆19Updated last year
- Align sequences and then parse features.☆18Updated 4 months ago
- python stuff I use☆19Updated 5 years ago
- R vignettes/pkgdown for elementary statistics for a summer course☆14Updated 7 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
- Color DNA/RNA bases in terminal output☆21Updated 7 years ago
- Easily run WDL workflows on GCP☆13Updated 3 years ago
- FAstqc DAta PArser - A minimal parser to parse FastQC output data.☆16Updated 9 years ago
- A catalogue of docker images for NGS data analysis tools☆9Updated 6 years ago
- A tool for running bioinformatics workflows locally or in the cloud.☆30Updated 5 years ago
- Lecture on viral phylodynamics☆12Updated 3 years ago
- Visualization and charting JS library for streaming genomic data☆19Updated 8 months ago
- Docker images of bioinformatics software☆21Updated 8 years ago
- ☆10Updated 7 years ago
- ☆13Updated 7 years ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 5 years ago
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 5 years ago
- Genomics Research Container Architecture☆48Updated 5 years ago
- Readshift: A method to shift high-quality NGS datasets into noisy datasets☆1Updated 6 years ago
- A lightweight Python graphing API for genomic features☆15Updated 3 years ago
- SVG based genome viewer written in javascript using D3☆33Updated 10 years ago
- What's The Function of these genes?☆22Updated 8 years ago
- Simplifies parallel processing of DNA sequencing reads☆9Updated 10 months ago
- Intersect multiple VCF files with haplotype awareness☆25Updated 4 years ago