bgruening / docker-galaxyLinks
Docker Images tracking the stable Galaxy releases.
☆234Updated this week
Alternatives and similar repositories for docker-galaxy
Users that are interested in docker-galaxy are comparing it to the libraries listed below
Sorting:
- A collection of Galaxy-related training material☆344Updated this week
- Command-line utilities to assist in developing Galaxy and Common Workflow Language artifacts - including tools, workflows, and training m…☆95Updated last week
- a lightweight db framework for exploring genetic variation.☆323Updated 5 years ago
- Nextflow Tower system☆151Updated 11 months ago
- A Python library for interacting with the Galaxy API☆95Updated last week
- CWL CommandLineTool descriptions for biology/life-sciences related applications☆80Updated 9 months ago
- BEDOPS: high-performance genomic feature operations☆356Updated 8 months ago
- Interactive web-based genome browser.☆228Updated 6 years ago
- Galaxy Admin Training☆60Updated last month
- Count bases in BAM/CRAM files☆322Updated 3 years ago
- Intuitive graphical web interface for running BLAST bioinformatics tool (i.e. have your own custom NCBI BLAST site!)☆293Updated last month
- A curated collection of Nextflow implementation patterns☆367Updated 2 years ago
- RTG Tools: Utilities for accurate VCF comparison and manipulation☆330Updated 7 months ago
- annotate a VCF with other VCFs/BEDs/tabixed files☆392Updated 4 months ago
- FlowCraft: a component-based pipeline composer for omics analysis using Nextflow.☆245Updated 4 months ago
- Documentation and description of AWS iGenomes S3 resource.☆119Updated last year
- Lollipop-style mutation diagrams for annotating genetic variations.☆195Updated last year
- Extension for Jupyter which integrates igv.js☆154Updated 3 years ago
- web-based analysis tool for rare disease genomics☆197Updated 2 weeks ago
- Automatic Filtering, Trimming, Error Removing and Quality Control for fastq data☆212Updated 5 years ago
- Detect germline or somatic variants from normal or tumour/normal whole-genome or targeted sequencing☆133Updated 5 years ago
- Example Nextflow pipelines and programming techniques☆106Updated 3 months ago
- Workflows for processing high-throughput sequencing data for variant discovery with GATK4 and related tools☆160Updated 3 years ago
- ☆117Updated 3 years ago
- Educational materials for learning WDL☆131Updated last year
- GFF and GVF specification documents☆219Updated last year
- A flexible framework for rapid genome analysis and interpretation☆317Updated 3 years ago
- Reference implementation of the APIs defined in ga4gh-schemas. RETIRED 2018-01-24☆99Updated 7 years ago
- Utilities for building and managing bioconda recipes☆103Updated this week
- HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.☆128Updated 5 years ago