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Reranking candidate gene models with cross-species comparison for improved gene prediction
BACKGROUND: Most gene finders score candidate gene models with state-based methods, typically HMMs, by combining local properties (coding potential, splice donor and acceptor patterns, etc). Competing models with similar state-based scores may be distinguishable with additional information. In parti...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2587481/ https://www.ncbi.nlm.nih.gov/pubmed/18854050 http://dx.doi.org/10.1186/1471-2105-9-433 |
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author | Liu, Qian Crammer, Koby Pereira, Fernando CN Roos, David S |
author_facet | Liu, Qian Crammer, Koby Pereira, Fernando CN Roos, David S |
author_sort | Liu, Qian |
collection | PubMed |
description | BACKGROUND: Most gene finders score candidate gene models with state-based methods, typically HMMs, by combining local properties (coding potential, splice donor and acceptor patterns, etc). Competing models with similar state-based scores may be distinguishable with additional information. In particular, functional and comparative genomics datasets may help to select among competing models of comparable probability by exploiting features likely to be associated with the correct gene models, such as conserved exon/intron structure or protein sequence features. RESULTS: We have investigated the utility of a simple post-processing step for selecting among a set of alternative gene models, using global scoring rules to rerank competing models for more accurate prediction. For each gene locus, we first generate the K best candidate gene models using the gene finder Evigan, and then rerank these models using comparisons with putative orthologous genes from closely-related species. Candidate gene models with lower scores in the original gene finder may be selected if they exhibit strong similarity to probable orthologs in coding sequence, splice site location, or signal peptide occurrence. Experiments on Drosophila melanogaster demonstrate that reranking based on cross-species comparison outperforms the best gene models identified by Evigan alone, and also outperforms the comparative gene finders GeneWise and Augustus+. CONCLUSION: Reranking gene models with cross-species comparison improves gene prediction accuracy. This straightforward method can be readily adapted to incorporate additional lines of evidence, as it requires only a ranked source of candidate gene models. |
format | Text |
id | pubmed-2587481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-25874812008-11-26 Reranking candidate gene models with cross-species comparison for improved gene prediction Liu, Qian Crammer, Koby Pereira, Fernando CN Roos, David S BMC Bioinformatics Methodology Article BACKGROUND: Most gene finders score candidate gene models with state-based methods, typically HMMs, by combining local properties (coding potential, splice donor and acceptor patterns, etc). Competing models with similar state-based scores may be distinguishable with additional information. In particular, functional and comparative genomics datasets may help to select among competing models of comparable probability by exploiting features likely to be associated with the correct gene models, such as conserved exon/intron structure or protein sequence features. RESULTS: We have investigated the utility of a simple post-processing step for selecting among a set of alternative gene models, using global scoring rules to rerank competing models for more accurate prediction. For each gene locus, we first generate the K best candidate gene models using the gene finder Evigan, and then rerank these models using comparisons with putative orthologous genes from closely-related species. Candidate gene models with lower scores in the original gene finder may be selected if they exhibit strong similarity to probable orthologs in coding sequence, splice site location, or signal peptide occurrence. Experiments on Drosophila melanogaster demonstrate that reranking based on cross-species comparison outperforms the best gene models identified by Evigan alone, and also outperforms the comparative gene finders GeneWise and Augustus+. CONCLUSION: Reranking gene models with cross-species comparison improves gene prediction accuracy. This straightforward method can be readily adapted to incorporate additional lines of evidence, as it requires only a ranked source of candidate gene models. BioMed Central 2008-10-14 /pmc/articles/PMC2587481/ /pubmed/18854050 http://dx.doi.org/10.1186/1471-2105-9-433 Text en Copyright © 2008 Liu 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 Liu, Qian Crammer, Koby Pereira, Fernando CN Roos, David S Reranking candidate gene models with cross-species comparison for improved gene prediction |
title | Reranking candidate gene models with cross-species comparison for improved gene prediction |
title_full | Reranking candidate gene models with cross-species comparison for improved gene prediction |
title_fullStr | Reranking candidate gene models with cross-species comparison for improved gene prediction |
title_full_unstemmed | Reranking candidate gene models with cross-species comparison for improved gene prediction |
title_short | Reranking candidate gene models with cross-species comparison for improved gene prediction |
title_sort | reranking candidate gene models with cross-species comparison for improved gene prediction |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2587481/ https://www.ncbi.nlm.nih.gov/pubmed/18854050 http://dx.doi.org/10.1186/1471-2105-9-433 |
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