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Model-based probe set optimization for high-performance microarrays
A major challenge in microarray design is the selection of highly specific oligonucleotide probes for all targeted genes of interest, while maintaining thermodynamic uniformity at the hybridization temperature. We introduce a novel microarray design framework (Thermodynamic Model-based Oligo Design...
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/PMC2647282/ https://www.ncbi.nlm.nih.gov/pubmed/19103659 http://dx.doi.org/10.1093/nar/gkn1001 |
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author | Leparc, Germán Gastón Tüchler, Thomas Striedner, Gerald Bayer, Karl Sykacek, Peter Hofacker, Ivo L. Kreil, David P. |
author_facet | Leparc, Germán Gastón Tüchler, Thomas Striedner, Gerald Bayer, Karl Sykacek, Peter Hofacker, Ivo L. Kreil, David P. |
author_sort | Leparc, Germán Gastón |
collection | PubMed |
description | A major challenge in microarray design is the selection of highly specific oligonucleotide probes for all targeted genes of interest, while maintaining thermodynamic uniformity at the hybridization temperature. We introduce a novel microarray design framework (Thermodynamic Model-based Oligo Design Optimizer, TherMODO) that for the first time incorporates a number of advanced modelling features: (i) A model of position-dependent labelling effects that is quantitatively derived from experiment. (ii) Multi-state thermodynamic hybridization models of probe binding behaviour, including potential cross-hybridization reactions. (iii) A fast calibrated sequence-similarity-based heuristic for cross-hybridization prediction supporting large-scale designs. (iv) A novel compound score formulation for the integrated assessment of multiple probe design objectives. In contrast to a greedy search for probes meeting parameter thresholds, this approach permits an optimization at the probe set level and facilitates the selection of highly specific probe candidates while maintaining probe set uniformity. (v) Lastly, a flexible target grouping structure allows easy adaptation of the pipeline to a variety of microarray application scenarios. The algorithm and features are discussed and demonstrated on actual design runs. Source code is available on request. |
format | Text |
id | pubmed-2647282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-26472822009-03-04 Model-based probe set optimization for high-performance microarrays Leparc, Germán Gastón Tüchler, Thomas Striedner, Gerald Bayer, Karl Sykacek, Peter Hofacker, Ivo L. Kreil, David P. Nucleic Acids Res Methods Online A major challenge in microarray design is the selection of highly specific oligonucleotide probes for all targeted genes of interest, while maintaining thermodynamic uniformity at the hybridization temperature. We introduce a novel microarray design framework (Thermodynamic Model-based Oligo Design Optimizer, TherMODO) that for the first time incorporates a number of advanced modelling features: (i) A model of position-dependent labelling effects that is quantitatively derived from experiment. (ii) Multi-state thermodynamic hybridization models of probe binding behaviour, including potential cross-hybridization reactions. (iii) A fast calibrated sequence-similarity-based heuristic for cross-hybridization prediction supporting large-scale designs. (iv) A novel compound score formulation for the integrated assessment of multiple probe design objectives. In contrast to a greedy search for probes meeting parameter thresholds, this approach permits an optimization at the probe set level and facilitates the selection of highly specific probe candidates while maintaining probe set uniformity. (v) Lastly, a flexible target grouping structure allows easy adaptation of the pipeline to a variety of microarray application scenarios. The algorithm and features are discussed and demonstrated on actual design runs. Source code is available on request. Oxford University Press 2009-02 2008-12-22 /pmc/articles/PMC2647282/ /pubmed/19103659 http://dx.doi.org/10.1093/nar/gkn1001 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 | Methods Online Leparc, Germán Gastón Tüchler, Thomas Striedner, Gerald Bayer, Karl Sykacek, Peter Hofacker, Ivo L. Kreil, David P. Model-based probe set optimization for high-performance microarrays |
title | Model-based probe set optimization for high-performance microarrays |
title_full | Model-based probe set optimization for high-performance microarrays |
title_fullStr | Model-based probe set optimization for high-performance microarrays |
title_full_unstemmed | Model-based probe set optimization for high-performance microarrays |
title_short | Model-based probe set optimization for high-performance microarrays |
title_sort | model-based probe set optimization for high-performance microarrays |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2647282/ https://www.ncbi.nlm.nih.gov/pubmed/19103659 http://dx.doi.org/10.1093/nar/gkn1001 |
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