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DNA motif elucidation using belief propagation
Protein-binding microarray (PBM) is a high-throughout platform that can measure the DNA-binding preference of a protein in a comprehensive and unbiased manner. A typical PBM experiment can measure binding signal intensities of a protein to all the possible DNA k-mers (k = 8 ∼10); such comprehensive...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763557/ https://www.ncbi.nlm.nih.gov/pubmed/23814189 http://dx.doi.org/10.1093/nar/gkt574 |
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author | Wong, Ka-Chun Chan, Tak-Ming Peng, Chengbin Li, Yue Zhang, Zhaolei |
author_facet | Wong, Ka-Chun Chan, Tak-Ming Peng, Chengbin Li, Yue Zhang, Zhaolei |
author_sort | Wong, Ka-Chun |
collection | PubMed |
description | Protein-binding microarray (PBM) is a high-throughout platform that can measure the DNA-binding preference of a protein in a comprehensive and unbiased manner. A typical PBM experiment can measure binding signal intensities of a protein to all the possible DNA k-mers (k = 8 ∼10); such comprehensive binding affinity data usually need to be reduced and represented as motif models before they can be further analyzed and applied. Since proteins can often bind to DNA in multiple modes, one of the major challenges is to decompose the comprehensive affinity data into multimodal motif representations. Here, we describe a new algorithm that uses Hidden Markov Models (HMMs) and can derive precise and multimodal motifs using belief propagations. We describe an HMM-based approach using belief propagations (kmerHMM), which accepts and preprocesses PBM probe raw data into median-binding intensities of individual k-mers. The k-mers are ranked and aligned for training an HMM as the underlying motif representation. Multiple motifs are then extracted from the HMM using belief propagations. Comparisons of kmerHMM with other leading methods on several data sets demonstrated its effectiveness and uniqueness. Especially, it achieved the best performance on more than half of the data sets. In addition, the multiple binding modes derived by kmerHMM are biologically meaningful and will be useful in interpreting other genome-wide data such as those generated from ChIP-seq. The executables and source codes are available at the authors’ websites: e.g. http://www.cs.toronto.edu/∼wkc/kmerHMM. |
format | Online Article Text |
id | pubmed-3763557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37635572013-09-10 DNA motif elucidation using belief propagation Wong, Ka-Chun Chan, Tak-Ming Peng, Chengbin Li, Yue Zhang, Zhaolei Nucleic Acids Res Methods Online Protein-binding microarray (PBM) is a high-throughout platform that can measure the DNA-binding preference of a protein in a comprehensive and unbiased manner. A typical PBM experiment can measure binding signal intensities of a protein to all the possible DNA k-mers (k = 8 ∼10); such comprehensive binding affinity data usually need to be reduced and represented as motif models before they can be further analyzed and applied. Since proteins can often bind to DNA in multiple modes, one of the major challenges is to decompose the comprehensive affinity data into multimodal motif representations. Here, we describe a new algorithm that uses Hidden Markov Models (HMMs) and can derive precise and multimodal motifs using belief propagations. We describe an HMM-based approach using belief propagations (kmerHMM), which accepts and preprocesses PBM probe raw data into median-binding intensities of individual k-mers. The k-mers are ranked and aligned for training an HMM as the underlying motif representation. Multiple motifs are then extracted from the HMM using belief propagations. Comparisons of kmerHMM with other leading methods on several data sets demonstrated its effectiveness and uniqueness. Especially, it achieved the best performance on more than half of the data sets. In addition, the multiple binding modes derived by kmerHMM are biologically meaningful and will be useful in interpreting other genome-wide data such as those generated from ChIP-seq. The executables and source codes are available at the authors’ websites: e.g. http://www.cs.toronto.edu/∼wkc/kmerHMM. Oxford University Press 2013-09 2013-06-29 /pmc/articles/PMC3763557/ /pubmed/23814189 http://dx.doi.org/10.1093/nar/gkt574 Text en © The Author(s) 2013. Published by Oxford University Press. 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 Wong, Ka-Chun Chan, Tak-Ming Peng, Chengbin Li, Yue Zhang, Zhaolei DNA motif elucidation using belief propagation |
title | DNA motif elucidation using belief propagation |
title_full | DNA motif elucidation using belief propagation |
title_fullStr | DNA motif elucidation using belief propagation |
title_full_unstemmed | DNA motif elucidation using belief propagation |
title_short | DNA motif elucidation using belief propagation |
title_sort | dna motif elucidation using belief propagation |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3763557/ https://www.ncbi.nlm.nih.gov/pubmed/23814189 http://dx.doi.org/10.1093/nar/gkt574 |
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