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A Model of the Statistical Power of Comparative Genome Sequence Analysis

Comparative genome sequence analysis is powerful, but sequencing genomes is expensive. It is desirable to be able to predict how many genomes are needed for comparative genomics, and at what evolutionary distances. Here I describe a simple mathematical model for the common problem of identifying con...

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Detalles Bibliográficos
Autor principal: Eddy, Sean R
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC539325/
https://www.ncbi.nlm.nih.gov/pubmed/15660152
http://dx.doi.org/10.1371/journal.pbio.0030010
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author Eddy, Sean R
author_facet Eddy, Sean R
author_sort Eddy, Sean R
collection PubMed
description Comparative genome sequence analysis is powerful, but sequencing genomes is expensive. It is desirable to be able to predict how many genomes are needed for comparative genomics, and at what evolutionary distances. Here I describe a simple mathematical model for the common problem of identifying conserved sequences. The model leads to some useful rules of thumb. For a given evolutionary distance, the number of comparative genomes needed for a constant level of statistical stringency in identifying conserved regions scales inversely with the size of the conserved feature to be detected. At short evolutionary distances, the number of comparative genomes required also scales inversely with distance. These scaling behaviors provide some intuition for future comparative genome sequencing needs, such as the proposed use of “phylogenetic shadowing” methods using closely related comparative genomes, and the feasibility of high-resolution detection of small conserved features.
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spelling pubmed-5393252005-01-04 A Model of the Statistical Power of Comparative Genome Sequence Analysis Eddy, Sean R PLoS Biol Research Article Comparative genome sequence analysis is powerful, but sequencing genomes is expensive. It is desirable to be able to predict how many genomes are needed for comparative genomics, and at what evolutionary distances. Here I describe a simple mathematical model for the common problem of identifying conserved sequences. The model leads to some useful rules of thumb. For a given evolutionary distance, the number of comparative genomes needed for a constant level of statistical stringency in identifying conserved regions scales inversely with the size of the conserved feature to be detected. At short evolutionary distances, the number of comparative genomes required also scales inversely with distance. These scaling behaviors provide some intuition for future comparative genome sequencing needs, such as the proposed use of “phylogenetic shadowing” methods using closely related comparative genomes, and the feasibility of high-resolution detection of small conserved features. Public Library of Science 2005-01 2005-01-04 /pmc/articles/PMC539325/ /pubmed/15660152 http://dx.doi.org/10.1371/journal.pbio.0030010 Text en Copyright: © 2005 Sean R. Eddy. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Eddy, Sean R
A Model of the Statistical Power of Comparative Genome Sequence Analysis
title A Model of the Statistical Power of Comparative Genome Sequence Analysis
title_full A Model of the Statistical Power of Comparative Genome Sequence Analysis
title_fullStr A Model of the Statistical Power of Comparative Genome Sequence Analysis
title_full_unstemmed A Model of the Statistical Power of Comparative Genome Sequence Analysis
title_short A Model of the Statistical Power of Comparative Genome Sequence Analysis
title_sort model of the statistical power of comparative genome sequence analysis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC539325/
https://www.ncbi.nlm.nih.gov/pubmed/15660152
http://dx.doi.org/10.1371/journal.pbio.0030010
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