Affiliation:
1. LIRMM, University of Montpellier, CNRS, Montpellier, France
2. SPYGEN, Le Bourget-du-Lac, France
Abstract
Abstract
Motivation
Novel recombinant viruses may have important medical and evolutionary significance, as they sometimes display new traits not present in the parental strains. This is particularly concerning when the new viruses combine fragments coming from phylogenetically distinct viral types. Here, we consider the task of screening large collections of sequences for such novel recombinants. A number of methods already exist for this task. However, these methods rely on complex models and heavy computations that are not always practical for a quick scan of a large number of sequences.
Results
We have developed SHERPAS, a new program to detect novel recombinants and provide a first estimate of their parental composition. Our approach is based on the precomputation of a large database of ‘phylogenetically-informed k-mers’, an idea recently introduced in the context of phylogenetic placement in metagenomics. Our experiments show that SHERPAS is hundreds to thousands of times faster than existing software, and enables the analysis of thousands of whole genomes, or long-sequencing reads, within minutes or seconds, and with limited loss of accuracy.
Availability and implementation
The source code is freely available for download at https://github.com/phylo42/sherpas.
Supplementary information
Supplementary data are available at Bioinformatics online.
Funder
ANR
The French National Research Agency
Investissements d'avenir" programme
Publisher
Oxford University Press (OUP)
Subject
Computational Mathematics,Computational Theory and Mathematics,Computer Science Applications,Molecular Biology,Biochemistry,Statistics and Probability
Cited by
2 articles.
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1. EPIK: precise and scalable evolutionary placement with informative k-mers;Bioinformatics;2023-11-17
2. Computing Phylo-$k$-Mers;IEEE/ACM Transactions on Computational Biology and Bioinformatics;2023