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STRAIN: an R package for multi-locus sequence typing from whole genome sequencing data

BACKGROUND: Multi-locus sequence typing (MLST) is a standard typing technique used to associate a sequence type (ST) to a bacterial isolate. When the output of whole genome sequencing (WGS) of a sample is available the ST can be assigned directly processing the read-set. Current approaches employ re...

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Autores principales: Dalsass, Mattia, Bodini, Margherita, Lambert, Christophe, Mortier, Marie-Cécile, Romanelli, Marco, Medini, Duccio, Muzzi, Alessandro, Brozzi, Alessandro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873635/
https://www.ncbi.nlm.nih.gov/pubmed/31757201
http://dx.doi.org/10.1186/s12859-019-2887-1
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author Dalsass, Mattia
Bodini, Margherita
Lambert, Christophe
Mortier, Marie-Cécile
Romanelli, Marco
Medini, Duccio
Muzzi, Alessandro
Brozzi, Alessandro
author_facet Dalsass, Mattia
Bodini, Margherita
Lambert, Christophe
Mortier, Marie-Cécile
Romanelli, Marco
Medini, Duccio
Muzzi, Alessandro
Brozzi, Alessandro
author_sort Dalsass, Mattia
collection PubMed
description BACKGROUND: Multi-locus sequence typing (MLST) is a standard typing technique used to associate a sequence type (ST) to a bacterial isolate. When the output of whole genome sequencing (WGS) of a sample is available the ST can be assigned directly processing the read-set. Current approaches employ reads mapping (SRST2) against the MLST loci, k-mer distribution (stringMLST), selective assembly (GRAbB) or whole genome assembly (BIGSdb) followed by BLASTn sequence query. Here we present STRAIN (ST Reduced Assembly IdentificatioN), an R package that implements a hybrid strategy between assembly and mapping of the reads to assign the ST to an isolate starting from its read-sets. RESULTS: Analysis of 540 publicly accessible Illumina read sets showed STRAIN to be more accurate at correct allele assignment and new alleles identification compared to SRTS2, stringMLST and GRAbB. STRAIN assigned correctly 3666 out of 3780 alleles (capability to identify correct alleles 97%) and, when presented with samples containing new alleles, identified them in 3730 out of 3780 STs (capability to identify new alleles 98.7%) of the cases. On the same dataset the other tested tools achieved lower capability to identify correct alleles (from 28.5 to 96.9%) and lower capability to identify new alleles (from 1.1 to 97.1%). CONCLUSIONS: STRAIN is a new accurate method to assign the alleles and ST to an isolate by processing the raw reads output of WGS. STRAIN is also able to retrieve new allele sequences if present. Capability to identify correct and new STs/alleles, evaluated on a benchmark dataset, are higher than other existing methods. STRAIN is designed for single allele typing as well as MLST. Its implementation in R makes allele and ST assignment simple, direct and prompt to be integrated in wider pipeline of downstream bioinformatics analyses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-2887-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-68736352019-11-25 STRAIN: an R package for multi-locus sequence typing from whole genome sequencing data Dalsass, Mattia Bodini, Margherita Lambert, Christophe Mortier, Marie-Cécile Romanelli, Marco Medini, Duccio Muzzi, Alessandro Brozzi, Alessandro BMC Bioinformatics Software BACKGROUND: Multi-locus sequence typing (MLST) is a standard typing technique used to associate a sequence type (ST) to a bacterial isolate. When the output of whole genome sequencing (WGS) of a sample is available the ST can be assigned directly processing the read-set. Current approaches employ reads mapping (SRST2) against the MLST loci, k-mer distribution (stringMLST), selective assembly (GRAbB) or whole genome assembly (BIGSdb) followed by BLASTn sequence query. Here we present STRAIN (ST Reduced Assembly IdentificatioN), an R package that implements a hybrid strategy between assembly and mapping of the reads to assign the ST to an isolate starting from its read-sets. RESULTS: Analysis of 540 publicly accessible Illumina read sets showed STRAIN to be more accurate at correct allele assignment and new alleles identification compared to SRTS2, stringMLST and GRAbB. STRAIN assigned correctly 3666 out of 3780 alleles (capability to identify correct alleles 97%) and, when presented with samples containing new alleles, identified them in 3730 out of 3780 STs (capability to identify new alleles 98.7%) of the cases. On the same dataset the other tested tools achieved lower capability to identify correct alleles (from 28.5 to 96.9%) and lower capability to identify new alleles (from 1.1 to 97.1%). CONCLUSIONS: STRAIN is a new accurate method to assign the alleles and ST to an isolate by processing the raw reads output of WGS. STRAIN is also able to retrieve new allele sequences if present. Capability to identify correct and new STs/alleles, evaluated on a benchmark dataset, are higher than other existing methods. STRAIN is designed for single allele typing as well as MLST. Its implementation in R makes allele and ST assignment simple, direct and prompt to be integrated in wider pipeline of downstream bioinformatics analyses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-019-2887-1) contains supplementary material, which is available to authorized users. BioMed Central 2019-11-22 /pmc/articles/PMC6873635/ /pubmed/31757201 http://dx.doi.org/10.1186/s12859-019-2887-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Software
Dalsass, Mattia
Bodini, Margherita
Lambert, Christophe
Mortier, Marie-Cécile
Romanelli, Marco
Medini, Duccio
Muzzi, Alessandro
Brozzi, Alessandro
STRAIN: an R package for multi-locus sequence typing from whole genome sequencing data
title STRAIN: an R package for multi-locus sequence typing from whole genome sequencing data
title_full STRAIN: an R package for multi-locus sequence typing from whole genome sequencing data
title_fullStr STRAIN: an R package for multi-locus sequence typing from whole genome sequencing data
title_full_unstemmed STRAIN: an R package for multi-locus sequence typing from whole genome sequencing data
title_short STRAIN: an R package for multi-locus sequence typing from whole genome sequencing data
title_sort strain: an r package for multi-locus sequence typing from whole genome sequencing data
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873635/
https://www.ncbi.nlm.nih.gov/pubmed/31757201
http://dx.doi.org/10.1186/s12859-019-2887-1
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