arq5x / ggdLinks
☆43Updated 9 years ago
Alternatives and similar repositories for ggd
Users that are interested in ggd are comparing it to the libraries listed below
Sorting:
- Response to blog post about Salmon☆37Updated 8 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- ☆36Updated 5 years ago
- What's The Function of these genes?☆22Updated 8 years ago
- sort genomic data☆36Updated 5 years ago
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 6 years ago
- Precursor to SnakeChunks, see https://github.com/SnakeChunks/SnakeChunks. This project has moved and will no longer be edited here.☆11Updated 8 years ago
- A tool for Read Multi-Mapper Resolution☆24Updated 8 years ago
- create a gemini-compatible database from a VCF☆56Updated 4 years ago
- Improved multi-sample transcript abundance estimates using adaptive priors☆20Updated 6 years ago
- fast webservices based query tool for large sets of genomic features☆25Updated 5 months ago
- Visualise interstrain recombination from environmental samples.☆26Updated 6 years ago
- Request for comments on interchangeable bioinformatics containers☆39Updated 6 years ago
- Making Snakemake workflows into full-fledged command line tools since 1999.☆51Updated 7 years ago
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- R Interface to the NCBI SRA metadata☆23Updated 6 years ago
- Color DNA/RNA bases in terminal output☆21Updated 8 years ago
- Qtip: a tandem simulation approach for accurately predicting read alignment mapping qualities☆25Updated 5 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆51Updated 10 months ago
- An awk-like VCF parser☆56Updated last year
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 8 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 10 months ago
- conda recipes for genomic data☆84Updated 4 years ago
- A versatile and efficient RNA-Seq read counting tool☆16Updated 9 years ago
- Peakzilla is a self-learning algorithm to identify transcription factor binding sites from ChIP-seq data. I would be very happy if you tr…☆20Updated last month
- Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model☆27Updated last year
- An algorithm for clonal tree reconstruction from multi-sample cancer sequencing data☆14Updated 7 years ago
- a wee tool for random access into BGZF files.☆85Updated 7 years ago
- ☆25Updated 4 years ago
- Import and run CWL workflows on DNAnexus (alpha)☆13Updated 7 years ago