arq5x / ggd
☆43Updated 8 years ago
Related projects: ⓘ
- This project has moved and will no longer be edited here. New link ->☆11Updated 7 years ago
- Homebrew formulae for bioinformatics software only available for Linux☆27Updated 5 years ago
- What's The Function of these genes?☆23Updated 7 years ago
- Stupid Simple Structural Variant View☆25Updated 7 years ago
- variant discovery and annotation using GATK and Ensembl☆17Updated 11 years ago
- Modeling and correcting fragment sequence bias for RNA-seq☆24Updated 3 months ago
- Response to blog post about Salmon☆37Updated 7 years ago
- Color DNA/RNA bases in terminal output☆20Updated 7 years ago
- fast webservices based query tool for large sets of genomic features☆25Updated last year
- ☆9Updated 7 years ago
- Stupid Simple Elastic Compute Cloud☆16Updated 9 months ago
- An algorithm for clonal tree reconstruction from multi-sample cancer sequencing data☆14Updated 6 years ago
- Parallel merging, squaring off and ensemble calling for genomic variants☆20Updated 5 years ago
- Improved multi-sample transcript abundance estimates using adaptive priors☆20Updated 5 years ago
- SMBL - SnakeMake Bioinformatics Library. Automatic installation of bioinformatics software in your SnakeMake pipelines.☆23Updated 7 years ago
- Metagenomic profiling and phylogenetic distances via common kmers☆42Updated 3 years ago
- Chanjo provides a better way to analyze coverage data in clinical sequencing.☆49Updated 3 months ago
- ☆18Updated 8 years ago
- BigWig manpulation tools using libBigWig and htslib☆28Updated last month
- Request for comments on interchangeable bioinformatics containers☆40Updated 5 years ago
- A hierarchical multiscale model for inferring transcription factor binding from chromatin accessibility data.☆25Updated 8 years ago
- High-definition reconstruction of clonal composition from next-generation sequencing data☆39Updated 8 years ago
- R package for extracting mutation signatures from a list of somatic mutations☆37Updated 5 years ago
- CheckQC inspects the content of an Illumina runfolder and determines if it passes a set of quality criteria☆24Updated last week
- ☆22Updated 7 years ago
- A tool for Read Multi-Mapper Resolution☆24Updated 7 years ago
- Rapid and robust analysis of RNA-Seq experiments.☆32Updated 8 years ago
- A Demultiplexing Tool for Illumina Sequencers☆10Updated 7 years ago
- A collection of well-known bioinformatics programs.☆25Updated 9 years ago