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:
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated last year
- What's The Function of these genes?☆22Updated 8 years ago
- Response to blog post about Salmon☆37Updated 7 years ago
- Precursor to SnakeChunks, see https://github.com/SnakeChunks/SnakeChunks. This project has moved and will no longer be edited here.☆11Updated 7 years ago
- ☆9Updated 8 years ago
- ☆37Updated 4 years ago
- Stupid Simple Structural Variant View☆25Updated 8 years ago
- fast webservices based query tool for large sets of genomic features☆25Updated 2 months ago
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 5 years ago
- BigWig manpulation tools using libBigWig and htslib☆29Updated 11 months ago
- A tool for Read Multi-Mapper Resolution☆23Updated 8 years ago
- R Interface to the NCBI SRA metadata☆23Updated 6 years ago
- Improved multi-sample transcript abundance estimates using adaptive priors☆20Updated 6 years ago
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 7 years ago
- ☆25Updated 4 years ago
- Request for comments on interchangeable bioinformatics containers☆40Updated 6 years ago
- Color DNA/RNA bases in terminal output☆21Updated 7 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆51Updated 7 months ago
- An awk-like VCF parser☆56Updated last year
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 7 months ago
- Making Snakemake workflows into full-fledged command line tools since 1999.☆52Updated 7 years ago
- Rapid and robust analysis of RNA-Seq experiments.☆32Updated 9 years ago
- CheckQC inspects the content of an Illumina runfolder and determines if it passes a set of quality criteria☆28Updated last week
- Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model☆27Updated last year
- R package for extracting mutation signatures from a list of somatic mutations☆37Updated 5 years ago
- sort genomic data☆35Updated 5 years ago
- Preprocessing tools for unique molecular index (UMI) sequencing reads☆31Updated 2 years ago
- Chromatin segmentation in R☆19Updated 7 years ago
- Code to reproduce analyses from the sleuth paper☆16Updated 6 years ago
- ☆22Updated 8 years ago