arq5x / ggd
☆43Updated 8 years ago
Alternatives and similar repositories for ggd:
Users that are interested in ggd are comparing it to the libraries listed below
- Stupid Simple Structural Variant View☆25Updated 8 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
- What's The Function of these genes?☆22Updated 7 years ago
- ☆37Updated 4 years ago
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 5 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated 7 months ago
- A tool for Read Multi-Mapper Resolution☆23Updated 7 years ago
- BigWig manpulation tools using libBigWig and htslib☆28Updated 5 months 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 last year
- Response to blog post about Salmon☆37Updated 7 years ago
- Stupid Simple Elastic Compute Cloud☆16Updated last year
- Making Snakemake workflows into full-fledged command line tools since 1999.☆51Updated 6 years ago
- ☆18Updated 9 years ago
- Chromatin segmentation in R☆19Updated 6 years ago
- ☆9Updated 8 years ago
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 7 years ago
- Enriched Domain Detector for ChIP-seq data☆16Updated 2 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆33Updated last month
- Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model☆27Updated last year
- R Interface to the NCBI SRA metadata☆23Updated 6 years ago
- Q ChIP-seq peak caller☆18Updated 6 months ago
- DEPRECIATED! Please use nf-core/tools instead☆19Updated 6 years ago
- Parallel merging, squaring off and ensemble calling for genomic variants☆20Updated 5 years ago
- Color DNA/RNA bases in terminal output☆20Updated 7 years ago
- Metagenomic profiling and phylogenetic distances via common kmers☆42Updated 3 years ago
- Import and run CWL workflows on DNAnexus (alpha)☆13Updated 6 years ago
- Run Picard on BAM files and collate 90 metrics into one file.☆39Updated 7 years ago
- ☆24Updated 4 years ago
- Rapid and robust analysis of RNA-Seq experiments.☆32Updated 8 years ago