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Absence/presence calling in microarray-based CGH experiments with non-model organisms
Structural variations in genomes are commonly studied by (micro)array-based comparative genomic hybridization. The data analysis methods to infer copy number variation in model organisms (human, mouse) are established. In principle, the procedures are based on signal ratios between test and referenc...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066771/ https://www.ncbi.nlm.nih.gov/pubmed/24771343 http://dx.doi.org/10.1093/nar/gku343 |
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author | Jonker, Martijs J. de Leeuw, Wim C. Marinković, Marino Wittink, Floyd R. A. Rauwerda, Han Bruning, Oskar Ensink, Wim A. Fluit, Ad C. Boel, C. H. de Jong, Mark Breit, Timo M. |
author_facet | Jonker, Martijs J. de Leeuw, Wim C. Marinković, Marino Wittink, Floyd R. A. Rauwerda, Han Bruning, Oskar Ensink, Wim A. Fluit, Ad C. Boel, C. H. de Jong, Mark Breit, Timo M. |
author_sort | Jonker, Martijs J. |
collection | PubMed |
description | Structural variations in genomes are commonly studied by (micro)array-based comparative genomic hybridization. The data analysis methods to infer copy number variation in model organisms (human, mouse) are established. In principle, the procedures are based on signal ratios between test and reference samples and the order of the probe targets in the genome. These procedures are less applicable to experiments with non-model organisms, which frequently comprise non-sequenced genomes with an unknown order of probe targets. We therefore present an additional analysis approach, which does not depend on the structural information of a reference genome, and quantifies the presence or absence of a probe target in an unknown genome. The principle is that intensity values of target probes are compared with the intensities of negative-control probes and positive-control probes from a control hybridization, to determine if a probe target is absent or present. In a test, analyzing the genome content of a known bacterial strain: Staphylococcus aureus MRSA252, this approach proved to be successful, demonstrated by receiver operating characteristic area under the curve values larger than 0.9995. We show its usability in various applications, such as comparing genome content and validating next-generation sequencing reads from eukaryotic non-model organisms. |
format | Online Article Text |
id | pubmed-4066771 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40667712014-06-24 Absence/presence calling in microarray-based CGH experiments with non-model organisms Jonker, Martijs J. de Leeuw, Wim C. Marinković, Marino Wittink, Floyd R. A. Rauwerda, Han Bruning, Oskar Ensink, Wim A. Fluit, Ad C. Boel, C. H. de Jong, Mark Breit, Timo M. Nucleic Acids Res Methods Online Structural variations in genomes are commonly studied by (micro)array-based comparative genomic hybridization. The data analysis methods to infer copy number variation in model organisms (human, mouse) are established. In principle, the procedures are based on signal ratios between test and reference samples and the order of the probe targets in the genome. These procedures are less applicable to experiments with non-model organisms, which frequently comprise non-sequenced genomes with an unknown order of probe targets. We therefore present an additional analysis approach, which does not depend on the structural information of a reference genome, and quantifies the presence or absence of a probe target in an unknown genome. The principle is that intensity values of target probes are compared with the intensities of negative-control probes and positive-control probes from a control hybridization, to determine if a probe target is absent or present. In a test, analyzing the genome content of a known bacterial strain: Staphylococcus aureus MRSA252, this approach proved to be successful, demonstrated by receiver operating characteristic area under the curve values larger than 0.9995. We show its usability in various applications, such as comparing genome content and validating next-generation sequencing reads from eukaryotic non-model organisms. Oxford University Press 2014-07-01 2014-04-25 /pmc/articles/PMC4066771/ /pubmed/24771343 http://dx.doi.org/10.1093/nar/gku343 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Jonker, Martijs J. de Leeuw, Wim C. Marinković, Marino Wittink, Floyd R. A. Rauwerda, Han Bruning, Oskar Ensink, Wim A. Fluit, Ad C. Boel, C. H. de Jong, Mark Breit, Timo M. Absence/presence calling in microarray-based CGH experiments with non-model organisms |
title | Absence/presence calling in microarray-based CGH experiments with non-model organisms |
title_full | Absence/presence calling in microarray-based CGH experiments with non-model organisms |
title_fullStr | Absence/presence calling in microarray-based CGH experiments with non-model organisms |
title_full_unstemmed | Absence/presence calling in microarray-based CGH experiments with non-model organisms |
title_short | Absence/presence calling in microarray-based CGH experiments with non-model organisms |
title_sort | absence/presence calling in microarray-based cgh experiments with non-model organisms |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066771/ https://www.ncbi.nlm.nih.gov/pubmed/24771343 http://dx.doi.org/10.1093/nar/gku343 |
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