CWL tools and workflows for GGR
☆22Oct 12, 2021Updated 4 years ago
Alternatives and similar repositories for GGR-cwl
Users that are interested in GGR-cwl are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- ☆11Oct 21, 2016Updated 9 years ago
- cwl-tes submits your tasks to a TES server. Task submission is parallelized when possible.☆19Mar 2, 2023Updated 3 years ago
- Galaxy container for single cell RNA-Seq tertiary analysis tools☆19Jun 26, 2025Updated last year
- ☆12Feb 19, 2021Updated 5 years ago
- Docker images of bioinformatics software☆21Jun 15, 2017Updated 9 years ago
- Managed hosting for WordPress and PHP on Cloudways • AdManaged hosting for WordPress, Magento, Laravel, or PHP apps, on multiple cloud providers. Deploy in minutes on Cloudways by DigitalOcean.
- CureFFI.org☆16Sep 2, 2026Updated 3 weeks ago
- Toil workflows for common genomic pipelines☆33Oct 3, 2019Updated 6 years ago
- yosef-ios☆11Jan 30, 2020Updated 6 years ago
- *UNOFFICIAL, UNMAINTAINED and OUTDATED*: This was an unofficial archive of GMAP-GSNAP releases. Please use the original website for curr…☆34Nov 1, 2015Updated 10 years ago
- Pipeline to call neoantigens from intron retention events derived from RNA-Seq data.☆29Feb 12, 2021Updated 5 years ago
- Population-scale single-cell RNA-seq profiling across dopaminergic neuron differentiation☆23Jun 28, 2024Updated 2 years ago
- GenomicsDB☆109Jan 3, 2023Updated 3 years ago
- Automated human exome/genome variants detection from FASTQ files☆23Sep 27, 2021Updated 4 years ago
- Detection of differential translated genes using Ribo-seq☆17Apr 10, 2021Updated 5 years ago
- Deploy to Railway using AI coding agents - Free Credits Offer • AdUse Claude Code, Codex, OpenCode, and more. Autonomous software development now has the infrastructure to match with Railway.
- localised duplicate detection on patterned flow cells☆10Feb 27, 2019Updated 7 years ago
- Filters for Next Generation Sequencing☆13Oct 31, 2024Updated last year
- Web client for CIViC: Clinical Interpretations of Variants in Cancer☆50Nov 28, 2023Updated 2 years ago
- direct comparison of circular and linear RNA expression☆24Jan 17, 2021Updated 5 years ago
- omniCLIP is a CLIP-Seq peak caller☆16Nov 14, 2020Updated 5 years ago
- Import and run CWL workflows on DNAnexus (alpha)☆13Sep 12, 2018Updated 8 years ago
- a peak-calling and differential analysis tool for replicated ChIP-Seq data☆37May 18, 2022Updated 4 years ago
- Deprecated☆101Aug 12, 2019Updated 7 years ago
- rf☆12Jul 29, 2026Updated last month
- 1-Click AI Models by DigitalOcean Gradient • AdDeploy popular AI models on DigitalOcean Gradient GPU virtual machines with just a single click. Zero configuration with optimized deployments.
- Biology-centered data-driven quality control for scRNA-seq☆21May 22, 2023Updated 3 years ago
- Scalable RNA-seq analysis☆73Jan 12, 2021Updated 5 years ago
- ☆16Updated this week
- robust matching of small variant datasets using flexible scoring schemes☆12Mar 26, 2020Updated 6 years ago
- A collection of command line tools for working with sequencing data☆52Updated this week
- PiGx SARS-CoV-2 wastewater sequencing pipeline☆18May 3, 2023Updated 3 years ago
- Comprehensive alignment, whole-genome coverage, and capture coverage statistics.☆20Dec 17, 2024Updated last year
- geneSurv: an interactive web-based tool for survival analysis in genomics research☆18Mar 17, 2020Updated 6 years ago
- Tutorial for working with cloud infrastructure and AWS from R☆20Jul 26, 2017Updated 9 years ago
- GPU virtual machines on DigitalOcean Gradient AI • AdGet to production fast with high-performance AMD and NVIDIA GPUs you can spin up in seconds. The definition of operational simplicity.
- JSON Schema validation for JSON-LD files using Schema.org vocabulary.☆24Dec 1, 2022Updated 3 years ago
- a simple lightweight workflow engine for data analysis scripting☆11Sep 5, 2019Updated 7 years ago
- ☆11May 27, 2024Updated 2 years ago
- splicing and feature maps for RBPs☆25Sep 8, 2026Updated 2 weeks ago
- Minimal Viable Identifier☆14Jan 21, 2022Updated 4 years ago
- HgvsGo is a program designed for analyzing "c." and "p." HGVS (Human Genome Variation Society) notations for single nucleotide variations…☆17Nov 20, 2024Updated last year
- ☆14Mar 8, 2017Updated 9 years ago