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Assessing the gene space in draft genomes

Genome sequencing projects have been initiated for a wide range of eukaryotes. A few projects have reached completion, but most exist as draft assemblies. As one of the main reasons to sequence a genome is to obtain its catalog of genes, an important question is how complete or completable the catal...

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Detalles Bibliográficos
Autores principales: Parra, Genis, Bradnam, Keith, Ning, Zemin, Keane, Thomas, Korf, Ian
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2615622/
https://www.ncbi.nlm.nih.gov/pubmed/19042974
http://dx.doi.org/10.1093/nar/gkn916
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author Parra, Genis
Bradnam, Keith
Ning, Zemin
Keane, Thomas
Korf, Ian
author_facet Parra, Genis
Bradnam, Keith
Ning, Zemin
Keane, Thomas
Korf, Ian
author_sort Parra, Genis
collection PubMed
description Genome sequencing projects have been initiated for a wide range of eukaryotes. A few projects have reached completion, but most exist as draft assemblies. As one of the main reasons to sequence a genome is to obtain its catalog of genes, an important question is how complete or completable the catalog is in unfinished genomes. To answer this question, we have identified a set of core eukaryotic genes (CEGs), that are extremely highly conserved and which we believe are present in low copy numbers in higher eukaryotes. From an analysis of a phylogenetically diverse set of eukaryotic genome assemblies, we found that the proportion of CEGs mapped in draft genomes provides a useful metric for describing the gene space, and complements the commonly used N50 length and x-fold coverage values.
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spelling pubmed-26156222009-03-30 Assessing the gene space in draft genomes Parra, Genis Bradnam, Keith Ning, Zemin Keane, Thomas Korf, Ian Nucleic Acids Res Genomics Genome sequencing projects have been initiated for a wide range of eukaryotes. A few projects have reached completion, but most exist as draft assemblies. As one of the main reasons to sequence a genome is to obtain its catalog of genes, an important question is how complete or completable the catalog is in unfinished genomes. To answer this question, we have identified a set of core eukaryotic genes (CEGs), that are extremely highly conserved and which we believe are present in low copy numbers in higher eukaryotes. From an analysis of a phylogenetically diverse set of eukaryotic genome assemblies, we found that the proportion of CEGs mapped in draft genomes provides a useful metric for describing the gene space, and complements the commonly used N50 length and x-fold coverage values. Oxford University Press 2009-01 2008-11-28 /pmc/articles/PMC2615622/ /pubmed/19042974 http://dx.doi.org/10.1093/nar/gkn916 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genomics
Parra, Genis
Bradnam, Keith
Ning, Zemin
Keane, Thomas
Korf, Ian
Assessing the gene space in draft genomes
title Assessing the gene space in draft genomes
title_full Assessing the gene space in draft genomes
title_fullStr Assessing the gene space in draft genomes
title_full_unstemmed Assessing the gene space in draft genomes
title_short Assessing the gene space in draft genomes
title_sort assessing the gene space in draft genomes
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2615622/
https://www.ncbi.nlm.nih.gov/pubmed/19042974
http://dx.doi.org/10.1093/nar/gkn916
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