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ICDS database: interrupted CoDing sequences in prokaryotic genomes
Unrecognized frameshifts, in-frame stop codons and sequencing errors lead to Interrupted CoDing Sequence (ICDS) that can seriously affect all subsequent steps of functional characterization, from in silico analysis to high-throughput proteomic projects. Here, we describe the Interrupted CoDing Seque...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1347423/ https://www.ncbi.nlm.nih.gov/pubmed/16381882 http://dx.doi.org/10.1093/nar/gkj060 |
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author | Perrodou, Emmanuel Deshayes, Caroline Muller, Jean Schaeffer, Christine Van Dorsselaer, Alain Ripp, Raymond Poch, Olivier Reyrat, Jean-Marc Lecompte, Odile |
author_facet | Perrodou, Emmanuel Deshayes, Caroline Muller, Jean Schaeffer, Christine Van Dorsselaer, Alain Ripp, Raymond Poch, Olivier Reyrat, Jean-Marc Lecompte, Odile |
author_sort | Perrodou, Emmanuel |
collection | PubMed |
description | Unrecognized frameshifts, in-frame stop codons and sequencing errors lead to Interrupted CoDing Sequence (ICDS) that can seriously affect all subsequent steps of functional characterization, from in silico analysis to high-throughput proteomic projects. Here, we describe the Interrupted CoDing Sequence database containing ICDS detected by a similarity-based approach in 80 complete prokaryotic genomes. ICDS can be retrieved by species browsing or similarity searches via a web interface (). The definition of each interrupted gene is provided as well as the ICDS genomic localization with the surrounding sequence. Furthermore, to facilitate the experimental characterization of ICDS, we propose optimized primers for re-sequencing purposes. The database will be regularly updated with additional data from ongoing sequenced genomes. Our strategy has been validated by three independent tests: (i) ICDS prediction on a benchmark of artificially created frameshifts, (ii) comparison of predicted ICDS and results obtained from the comparison of the two genomic sequences of Bacillus licheniformis strain ATCC 14580 and (iii) re-sequencing of 25 predicted ICDS of the recently sequenced genome of Mycobacterium smegmatis. This allows us to estimate the specificity and sensitivity (95 and 82%, respectively) of our program and the efficiency of primer determination. |
format | Text |
id | pubmed-1347423 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-13474232006-01-25 ICDS database: interrupted CoDing sequences in prokaryotic genomes Perrodou, Emmanuel Deshayes, Caroline Muller, Jean Schaeffer, Christine Van Dorsselaer, Alain Ripp, Raymond Poch, Olivier Reyrat, Jean-Marc Lecompte, Odile Nucleic Acids Res Article Unrecognized frameshifts, in-frame stop codons and sequencing errors lead to Interrupted CoDing Sequence (ICDS) that can seriously affect all subsequent steps of functional characterization, from in silico analysis to high-throughput proteomic projects. Here, we describe the Interrupted CoDing Sequence database containing ICDS detected by a similarity-based approach in 80 complete prokaryotic genomes. ICDS can be retrieved by species browsing or similarity searches via a web interface (). The definition of each interrupted gene is provided as well as the ICDS genomic localization with the surrounding sequence. Furthermore, to facilitate the experimental characterization of ICDS, we propose optimized primers for re-sequencing purposes. The database will be regularly updated with additional data from ongoing sequenced genomes. Our strategy has been validated by three independent tests: (i) ICDS prediction on a benchmark of artificially created frameshifts, (ii) comparison of predicted ICDS and results obtained from the comparison of the two genomic sequences of Bacillus licheniformis strain ATCC 14580 and (iii) re-sequencing of 25 predicted ICDS of the recently sequenced genome of Mycobacterium smegmatis. This allows us to estimate the specificity and sensitivity (95 and 82%, respectively) of our program and the efficiency of primer determination. Oxford University Press 2006-01-01 2005-12-28 /pmc/articles/PMC1347423/ /pubmed/16381882 http://dx.doi.org/10.1093/nar/gkj060 Text en © The Author 2006. Published by Oxford University Press. All rights reserved |
spellingShingle | Article Perrodou, Emmanuel Deshayes, Caroline Muller, Jean Schaeffer, Christine Van Dorsselaer, Alain Ripp, Raymond Poch, Olivier Reyrat, Jean-Marc Lecompte, Odile ICDS database: interrupted CoDing sequences in prokaryotic genomes |
title | ICDS database: interrupted CoDing sequences in prokaryotic genomes |
title_full | ICDS database: interrupted CoDing sequences in prokaryotic genomes |
title_fullStr | ICDS database: interrupted CoDing sequences in prokaryotic genomes |
title_full_unstemmed | ICDS database: interrupted CoDing sequences in prokaryotic genomes |
title_short | ICDS database: interrupted CoDing sequences in prokaryotic genomes |
title_sort | icds database: interrupted coding sequences in prokaryotic genomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1347423/ https://www.ncbi.nlm.nih.gov/pubmed/16381882 http://dx.doi.org/10.1093/nar/gkj060 |
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