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Clustering evolving proteins into homologous families

BACKGROUND: Clustering sequences into groups of putative homologs (families) is a critical first step in many areas of comparative biology and bioinformatics. The performance of clustering approaches in delineating biologically meaningful families depends strongly on characteristics of the data, inc...

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Autores principales: Chan, Cheong Xin, Mahbob, Maisarah, Ragan, Mark A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3637521/
https://www.ncbi.nlm.nih.gov/pubmed/23566217
http://dx.doi.org/10.1186/1471-2105-14-120
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author Chan, Cheong Xin
Mahbob, Maisarah
Ragan, Mark A
author_facet Chan, Cheong Xin
Mahbob, Maisarah
Ragan, Mark A
author_sort Chan, Cheong Xin
collection PubMed
description BACKGROUND: Clustering sequences into groups of putative homologs (families) is a critical first step in many areas of comparative biology and bioinformatics. The performance of clustering approaches in delineating biologically meaningful families depends strongly on characteristics of the data, including content bias and degree of divergence. New, highly scalable methods have recently been introduced to cluster the very large datasets being generated by next-generation sequencing technologies. However, there has been little systematic investigation of how characteristics of the data impact the performance of these approaches. RESULTS: Using clusters from a manually curated dataset as reference, we examined the performance of a widely used graph-based Markov clustering algorithm (MCL) and a greedy heuristic approach (UCLUST) in delineating protein families coded by three sets of bacterial genomes of different G+C content. Both MCL and UCLUST generated clusters that are comparable to the reference sets at specific parameter settings, although UCLUST tends to under-cluster compositionally biased sequences (G+C content 33% and 66%). Using simulated data, we sought to assess the individual effects of sequence divergence, rate heterogeneity, and underlying G+C content. Performance decreased with increasing sequence divergence, decreasing among-site rate variation, and increasing G+C bias. Two MCL-based methods recovered the simulated families more accurately than did UCLUST. MCL using local alignment distances is more robust across the investigated range of sequence features than are greedy heuristics using distances based on global alignment. CONCLUSIONS: Our results demonstrate that sequence divergence, rate heterogeneity and content bias can individually and in combination affect the accuracy with which MCL and UCLUST can recover homologous protein families. For application to data that are more divergent, and exhibit higher among-site rate variation and/or content bias, MCL may often be the better choice, especially if computational resources are not limiting.
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spelling pubmed-36375212013-04-27 Clustering evolving proteins into homologous families Chan, Cheong Xin Mahbob, Maisarah Ragan, Mark A BMC Bioinformatics Methodology Article BACKGROUND: Clustering sequences into groups of putative homologs (families) is a critical first step in many areas of comparative biology and bioinformatics. The performance of clustering approaches in delineating biologically meaningful families depends strongly on characteristics of the data, including content bias and degree of divergence. New, highly scalable methods have recently been introduced to cluster the very large datasets being generated by next-generation sequencing technologies. However, there has been little systematic investigation of how characteristics of the data impact the performance of these approaches. RESULTS: Using clusters from a manually curated dataset as reference, we examined the performance of a widely used graph-based Markov clustering algorithm (MCL) and a greedy heuristic approach (UCLUST) in delineating protein families coded by three sets of bacterial genomes of different G+C content. Both MCL and UCLUST generated clusters that are comparable to the reference sets at specific parameter settings, although UCLUST tends to under-cluster compositionally biased sequences (G+C content 33% and 66%). Using simulated data, we sought to assess the individual effects of sequence divergence, rate heterogeneity, and underlying G+C content. Performance decreased with increasing sequence divergence, decreasing among-site rate variation, and increasing G+C bias. Two MCL-based methods recovered the simulated families more accurately than did UCLUST. MCL using local alignment distances is more robust across the investigated range of sequence features than are greedy heuristics using distances based on global alignment. CONCLUSIONS: Our results demonstrate that sequence divergence, rate heterogeneity and content bias can individually and in combination affect the accuracy with which MCL and UCLUST can recover homologous protein families. For application to data that are more divergent, and exhibit higher among-site rate variation and/or content bias, MCL may often be the better choice, especially if computational resources are not limiting. BioMed Central 2013-04-08 /pmc/articles/PMC3637521/ /pubmed/23566217 http://dx.doi.org/10.1186/1471-2105-14-120 Text en Copyright © 2013 Chan et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology Article
Chan, Cheong Xin
Mahbob, Maisarah
Ragan, Mark A
Clustering evolving proteins into homologous families
title Clustering evolving proteins into homologous families
title_full Clustering evolving proteins into homologous families
title_fullStr Clustering evolving proteins into homologous families
title_full_unstemmed Clustering evolving proteins into homologous families
title_short Clustering evolving proteins into homologous families
title_sort clustering evolving proteins into homologous families
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3637521/
https://www.ncbi.nlm.nih.gov/pubmed/23566217
http://dx.doi.org/10.1186/1471-2105-14-120
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