arvados / lightning-server-legacyLinks
lightning
☆11Updated 9 years ago
Alternatives and similar repositories for lightning-server-legacy
Users that are interested in lightning-server-legacy are comparing it to the libraries listed below
Sorting:
- Parallel Recipes : parallel workflow execution made easy☆13Updated 9 years ago
- ☆12Updated 8 years ago
- Novel Adjacency Identification with Barcoded Reads☆13Updated 3 years ago
- Benchmarking toolkit for variant calling☆47Updated 4 years ago
- robust matching of small variant datasets using flexible scoring schemes☆11Updated 5 years ago
- Home of the Genomic Feature and Variation Ontology (GFVO)☆16Updated 4 years ago
- SNAPR: a bioinformatics pipeline for efficient and accurate RNA-seq alignment and analysis☆25Updated 10 years ago
- GenoTypes Compressor☆15Updated 3 years ago
- Basic, no assumptions, multi-pileup☆24Updated 11 years ago
- [Bio in Docker] Symposium 2015☆21Updated 7 years ago
- variant integration methods for the 1000 Genomes Project☆21Updated 7 years ago
- Online material and code base for the article Coordinates and Intervals in Graph Based Reference Genomes☆11Updated 8 years ago
- pythonic wrapper for libhts (moved to: https://github.com/quinlan-lab/hts-python)☆49Updated 8 years ago
- Inferring spatiotemporal dynamics of the H1N1 influenza pandemic from sequence data☆32Updated 11 years ago
- Trigger the Google Genomics Pipeline API with CWL☆11Updated 8 years ago
- Lightweight workflows in bioinformatics:☆24Updated 10 years ago
- [Experimental] Workflow Definition Language (WDL) to CWL☆28Updated 3 years ago
- A genomics pipeline build on top of the GATK Queue framework. Main repository: https://github.com/NationalGenomicsInfrastructure/piper (m…☆21Updated 8 years ago
- Toil workflows for common genomic pipelines☆33Updated 5 years ago
- High throughput, pain-free big data pipelines.☆30Updated 8 years ago
- Directly create a bigwig file with signal derived from a sorted and indexed bam file.☆11Updated 8 years ago
- ☆45Updated 9 years ago
- I have put my modified version of the deepbind code here.☆8Updated 9 years ago
- Quality control methods for human genomic variants.☆62Updated 2 years ago
- Seqnature: incorporate SNPs and Indels into a reference genome☆16Updated 8 years ago
- Python graph database framework for bioinformatics☆93Updated 3 years ago
- Graphical assessment of structrial variants using 10x genomics data☆10Updated 8 years ago
- This BLENDER has been sunsetted☆16Updated 9 months ago
- Curated collection of open-source bioinformatics tools☆28Updated 6 years ago
- ☆15Updated 9 years ago