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Compressive Sensing DNA Microarrays

Compressive sensing microarrays (CSMs) are DNA-based sensors that operate using group testing and compressive sensing (CS) principles. In contrast to conventional DNA microarrays, in which each genetic sensor is designed to respond to a single target, in a CSM, each sensor responds to a set of targe...

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Detalles Bibliográficos
Autores principales: Dai, Wei, Sheikh, Mona A, Milenkovic, Olgica, Baraniuk, Richard G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171419/
https://www.ncbi.nlm.nih.gov/pubmed/19158952
http://dx.doi.org/10.1155/2009/162824
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author Dai, Wei
Sheikh, Mona A
Milenkovic, Olgica
Baraniuk, Richard G
author_facet Dai, Wei
Sheikh, Mona A
Milenkovic, Olgica
Baraniuk, Richard G
author_sort Dai, Wei
collection PubMed
description Compressive sensing microarrays (CSMs) are DNA-based sensors that operate using group testing and compressive sensing (CS) principles. In contrast to conventional DNA microarrays, in which each genetic sensor is designed to respond to a single target, in a CSM, each sensor responds to a set of targets. We study the problem of designing CSMs that simultaneously account for both the constraints from CS theory and the biochemistry of probe-target DNA hybridization. An appropriate cross-hybridization model is proposed for CSMs, and several methods are developed for probe design and CS signal recovery based on the new model. Lab experiments suggest that in order to achieve accurate hybridization profiling, consensus probe sequences are required to have sequence homology of at least 80% with all targets to be detected. Furthermore, out-of-equilibrium datasets are usually as accurate as those obtained from equilibrium conditions. Consequently, one can use CSMs in applications in which only short hybridization times are allowed.
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spelling pubmed-31714192011-09-13 Compressive Sensing DNA Microarrays Dai, Wei Sheikh, Mona A Milenkovic, Olgica Baraniuk, Richard G EURASIP J Bioinform Syst Biol Research Article Compressive sensing microarrays (CSMs) are DNA-based sensors that operate using group testing and compressive sensing (CS) principles. In contrast to conventional DNA microarrays, in which each genetic sensor is designed to respond to a single target, in a CSM, each sensor responds to a set of targets. We study the problem of designing CSMs that simultaneously account for both the constraints from CS theory and the biochemistry of probe-target DNA hybridization. An appropriate cross-hybridization model is proposed for CSMs, and several methods are developed for probe design and CS signal recovery based on the new model. Lab experiments suggest that in order to achieve accurate hybridization profiling, consensus probe sequences are required to have sequence homology of at least 80% with all targets to be detected. Furthermore, out-of-equilibrium datasets are usually as accurate as those obtained from equilibrium conditions. Consequently, one can use CSMs in applications in which only short hybridization times are allowed. Springer 2008-12-22 /pmc/articles/PMC3171419/ /pubmed/19158952 http://dx.doi.org/10.1155/2009/162824 Text en Copyright © 2009 Wei Dai et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Dai, Wei
Sheikh, Mona A
Milenkovic, Olgica
Baraniuk, Richard G
Compressive Sensing DNA Microarrays
title Compressive Sensing DNA Microarrays
title_full Compressive Sensing DNA Microarrays
title_fullStr Compressive Sensing DNA Microarrays
title_full_unstemmed Compressive Sensing DNA Microarrays
title_short Compressive Sensing DNA Microarrays
title_sort compressive sensing dna microarrays
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3171419/
https://www.ncbi.nlm.nih.gov/pubmed/19158952
http://dx.doi.org/10.1155/2009/162824
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