V-pipe
V-pipe is a tool for creating workflows to analyze next-generation sequencing (NGS) data from viral pathogens. V-pipe can output many results in various formats, such as SNV calls, local and global haplotypes, and consensus sequences. A version of the V-pipe to analyze high-throughput sequencing data of SARS-CoV-2 is available. See 'links.'
Topic
Genomics;Population genetics;Workflows
Detail
Operation: Sequence alignment;Genetic variation analysis
Software interface: Command-line user interface;Workflow
Language: Shell;Python
License: Apache-2.0
Cost: Free
Version name: 2.99.1
Credit: -
Input: Organized in a two-level directory hierarchy, and the sequencing reads must be provided in a sub-folder named raw_data.
Output: -
Contact: susana.posada@bsse.ethz.ch;david.seifert@bsse.ethz.ch;niko.beerenwinkel@bsse.ethz.ch;ivan.topolsky@sib.swiss;v-pipe@bsse.ethz.ch
Collection: -
Maturity: Stable
Publications
- Recent advances in inferring viral diversity from high-throughput sequencing data.
- Posada-Cespedes S, Seifert D, Beerenwinkel N. Recent advances in inferring viral diversity from high-throughput sequencing data. Virus Res. 2017 Jul 15;239:17-32. doi: 10.1016/j.virusres.2016.09.016. Epub 2016 Sep 28. PMID: 27693290.
- https://doi.org/10.1016/j.virusres.2016.09.016
- PMID: 27693290
- PMC: -
Download and documentation
Documentation: https://cbg-ethz.github.io/V-pipe/usage/
Home page: https://cbg-ethz.github.io/V-pipe/
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