nf-core-viralrecon
nfcore/viralrecon is a bioinformatics analysis pipeline used to perform assembly and intra-host/low-frequency variant calling for viral samples. The pipeline supports short-read Illumina sequencing data from both shotgun (e.g. sequencing directly from clinical samples) and enrichment-based library preparation methods (e.g. amplicon-based: ARTIC SARS-CoV-2 enrichment protocol; or probe-capture-based).
Topics
Collections
Details
- License:
- MIT
- Maturity:
- Mature
- Cost:
- Free of charge
- Tool Type:
- command-line tool, workflow
- Operating Systems:
- Linux
- Programming Languages:
- Groovy
- Added:
- 1/13/2021
- Last Updated:
- 3/11/2022
Operations
Data Inputs & Outputs
Genetic variation analysis
Outputs
Publications
Ewels PA, Peltzer A, Fillinger S, Patel H, Alneberg J, Wilm A, Garcia MU, Di Tommaso P, Nahnsen S. The nf-core framework for community-curated bioinformatics pipelines. Nature Biotechnology. 2020;38(3):276-278. doi:10.1038/s41587-020-0439-x. PMID:32055031.
PMID: 32055031
Funding: - EC | Horizon 2020 Framework Programme: 815668 (BovReg)
- Deutsche Forschungsgemeinschaft: 398967434–TRR 261, KO-2313/6-2, Liver Cancer SFB/TR 209
Documentation
General
https://nf-co.re/viralreconUser manual
https://nf-co.re/viralrecon/usageDownloads
- Source codeVersion: 2.4.1https://github.com/nf-core/viralrecon/releases/tag/2.4.1Release 1.1.0