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EasyGene – a prokaryotic gene finder that ranks ORFs by statistical significance
BACKGROUND: Contrary to other areas of sequence analysis, a measure of statistical significance of a putative gene has not been devised to help in discriminating real genes from the masses of random Open Reading Frames (ORFs) in prokaryotic genomes. Therefore, many genomes have too many short ORFs a...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC521197/ https://www.ncbi.nlm.nih.gov/pubmed/12783628 http://dx.doi.org/10.1186/1471-2105-4-21 |
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author | Larsen, Thomas Schou Krogh, Anders |
author_facet | Larsen, Thomas Schou Krogh, Anders |
author_sort | Larsen, Thomas Schou |
collection | PubMed |
description | BACKGROUND: Contrary to other areas of sequence analysis, a measure of statistical significance of a putative gene has not been devised to help in discriminating real genes from the masses of random Open Reading Frames (ORFs) in prokaryotic genomes. Therefore, many genomes have too many short ORFs annotated as genes. RESULTS: In this paper, we present a new automated gene-finding method, EasyGene, which estimates the statistical significance of a predicted gene. The gene finder is based on a hidden Markov model (HMM) that is automatically estimated for a new genome. Using extensions of similarities in Swiss-Prot, a high quality training set of genes is automatically extracted from the genome and used to estimate the HMM. Putative genes are then scored with the HMM, and based on score and length of an ORF, the statistical significance is calculated. The measure of statistical significance for an ORF is the expected number of ORFs in one megabase of random sequence at the same significance level or better, where the random sequence has the same statistics as the genome in the sense of a third order Markov chain. CONCLUSIONS: The result is a flexible gene finder whose overall performance matches or exceeds other methods. The entire pipeline of computer processing from the raw input of a genome or set of contigs to a list of putative genes with significance is automated, making it easy to apply EasyGene to newly sequenced organisms. EasyGene with pre-trained models can be accessed at . |
format | Text |
id | pubmed-521197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5211972004-10-04 EasyGene – a prokaryotic gene finder that ranks ORFs by statistical significance Larsen, Thomas Schou Krogh, Anders BMC Bioinformatics Research Article BACKGROUND: Contrary to other areas of sequence analysis, a measure of statistical significance of a putative gene has not been devised to help in discriminating real genes from the masses of random Open Reading Frames (ORFs) in prokaryotic genomes. Therefore, many genomes have too many short ORFs annotated as genes. RESULTS: In this paper, we present a new automated gene-finding method, EasyGene, which estimates the statistical significance of a predicted gene. The gene finder is based on a hidden Markov model (HMM) that is automatically estimated for a new genome. Using extensions of similarities in Swiss-Prot, a high quality training set of genes is automatically extracted from the genome and used to estimate the HMM. Putative genes are then scored with the HMM, and based on score and length of an ORF, the statistical significance is calculated. The measure of statistical significance for an ORF is the expected number of ORFs in one megabase of random sequence at the same significance level or better, where the random sequence has the same statistics as the genome in the sense of a third order Markov chain. CONCLUSIONS: The result is a flexible gene finder whose overall performance matches or exceeds other methods. The entire pipeline of computer processing from the raw input of a genome or set of contigs to a list of putative genes with significance is automated, making it easy to apply EasyGene to newly sequenced organisms. EasyGene with pre-trained models can be accessed at . BioMed Central 2003-06-03 /pmc/articles/PMC521197/ /pubmed/12783628 http://dx.doi.org/10.1186/1471-2105-4-21 Text en Copyright © 2003 Larsen and Krogh; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Article Larsen, Thomas Schou Krogh, Anders EasyGene – a prokaryotic gene finder that ranks ORFs by statistical significance |
title | EasyGene – a prokaryotic gene finder that ranks ORFs by statistical significance |
title_full | EasyGene – a prokaryotic gene finder that ranks ORFs by statistical significance |
title_fullStr | EasyGene – a prokaryotic gene finder that ranks ORFs by statistical significance |
title_full_unstemmed | EasyGene – a prokaryotic gene finder that ranks ORFs by statistical significance |
title_short | EasyGene – a prokaryotic gene finder that ranks ORFs by statistical significance |
title_sort | easygene – a prokaryotic gene finder that ranks orfs by statistical significance |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC521197/ https://www.ncbi.nlm.nih.gov/pubmed/12783628 http://dx.doi.org/10.1186/1471-2105-4-21 |
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