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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...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2009
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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. |
format | Text |
id | pubmed-2615622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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