snakemake-workflows / docsLinks
Documentation of the Snakemake-Workflows project
☆156Updated 3 years ago
Alternatives and similar repositories for docs
Users that are interested in docs are comparing it to the libraries listed below
Sorting:
- Light-weight Snakemake workflow for preprocessing and statistical analysis of RNA-seq data☆165Updated 7 months ago
- Intervene: a tool for intersection and visualization of multiple genomic region and gene sets☆141Updated last year
- dN/dS methods to quantify selection in cancer and somatic evolution☆222Updated 2 months ago
- RNA-Seq analysis workflow☆104Updated 4 years ago
- minimal example implementations for bioinformatics workflow managers☆276Updated 3 years ago
- Learning the Variant Call Format☆140Updated last year
- Example Nextflow pipelines and programming techniques☆107Updated 2 months ago
- Basic operations on the space of numerical functions defined on the genome using lazy evaluators for flexibility and efficiency☆151Updated 8 months ago
- Demonstrating best practices for bioinformatics command line tools☆117Updated 4 years ago
- NGS-pipe: next-generation sequencing pipelines for precision oncology☆111Updated 6 years ago
- Genomic Interactive Visualization Engine☆145Updated 2 years ago
- A collection of scripts and notes related to genomics and bioinformatics☆214Updated 3 months ago
- GATK RNA-Seq Variant Calling in Nextflow☆133Updated 2 years ago
- Web application to explore the Sequence Read Archive.☆218Updated 3 months ago
- GWAS Pipeline for H3Africa☆110Updated last month
- TPMCalculator quantifies mRNA abundance directly from the alignments by parsing BAM files☆130Updated last year
- Automated and customizable preprocessing of Next-Generation Sequencing data, including full (sc)ATAC-seq, ChIP-seq, and (sc)RNA-seq workf…☆163Updated 2 months ago
- a snakemake pipeline to process ChIP-seq files from GEO or in-house☆108Updated 5 years ago
- Statistical Analysis of RNA-Seq Tools☆107Updated 3 months ago
- Transcript quantification import for modular pipelines☆139Updated 2 weeks ago
- HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.☆102Updated last month
- This is the development home of the Snakemake wrapper repository, see☆231Updated this week
- Visualizing transcript structure and annotation using ggplot2☆158Updated 10 months ago
- Documentation and description of AWS iGenomes S3 resource.☆114Updated 7 months ago
- R package for extracting and visualizing mutational patterns in base substitution catalogues☆106Updated 2 years ago
- Annotation-free quantification of RNA splicing. Yang I. Li, David A. Knowles, Jack Humphrey, Alvaro N. Barbeira, Scott P. Dickinson, Hae …☆221Updated last year
- Automated generation of tailored bioinformatics Jupyter Notebooks via a user interface.☆115Updated last month
- Suite of motif tools, including a motif prediction pipeline for ChIP-seq experiments. See full GimmeMotifs documentation for detailed in…☆120Updated last year
- A (mostly) universal methylation extractor for BS-seq experiments.☆173Updated last year
- Tutorials on accessing public reference and genomic data☆30Updated 4 months ago