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Tree-Based Position Weight Matrix Approach to Model Transcription Factor Binding Site Profiles
Most of the position weight matrix (PWM) based bioinformatics methods developed to predict transcription factor binding sites (TFBS) assume each nucleotide in the sequence motif contributes independently to the interaction between protein and DNA sequence, usually producing high false positive predi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166302/ https://www.ncbi.nlm.nih.gov/pubmed/21912677 http://dx.doi.org/10.1371/journal.pone.0024210 |
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author | Bi, Yingtao Kim, Hyunsoo Gupta, Ravi Davuluri, Ramana V. |
author_facet | Bi, Yingtao Kim, Hyunsoo Gupta, Ravi Davuluri, Ramana V. |
author_sort | Bi, Yingtao |
collection | PubMed |
description | Most of the position weight matrix (PWM) based bioinformatics methods developed to predict transcription factor binding sites (TFBS) assume each nucleotide in the sequence motif contributes independently to the interaction between protein and DNA sequence, usually producing high false positive predictions. The increasing availability of TF enrichment profiles from recent ChIP-Seq methodology facilitates the investigation of dependent structure and accurate prediction of TFBSs. We develop a novel Tree-based PWM (TPWM) approach to accurately model the interaction between TF and its binding site. The whole tree-structured PWM could be considered as a mixture of different conditional-PWMs. We propose a discriminative approach, called TPD (TPWM based Discriminative Approach), to construct the TPWM from the ChIP-Seq data with a pre-existing PWM. To achieve the maximum discriminative power between the positive and negative datasets, the cutoff value is determined based on the Matthew Correlation Coefficient (MCC). The resulting TPWMs are evaluated with respect to accuracy on extensive synthetic datasets. We then apply our TPWM discriminative approach on several real ChIP-Seq datasets to refine the current TFBS models stored in the TRANSFAC database. Experiments on both the simulated and real ChIP-Seq data show that the proposed method starting from existing PWM has consistently better performance than existing tools in detecting the TFBSs. The improved accuracy is the result of modelling the complete dependent structure of the motifs and better prediction of true positive rate. The findings could lead to better understanding of the mechanisms of TF-DNA interactions. |
format | Online Article Text |
id | pubmed-3166302 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31663022011-09-12 Tree-Based Position Weight Matrix Approach to Model Transcription Factor Binding Site Profiles Bi, Yingtao Kim, Hyunsoo Gupta, Ravi Davuluri, Ramana V. PLoS One Research Article Most of the position weight matrix (PWM) based bioinformatics methods developed to predict transcription factor binding sites (TFBS) assume each nucleotide in the sequence motif contributes independently to the interaction between protein and DNA sequence, usually producing high false positive predictions. The increasing availability of TF enrichment profiles from recent ChIP-Seq methodology facilitates the investigation of dependent structure and accurate prediction of TFBSs. We develop a novel Tree-based PWM (TPWM) approach to accurately model the interaction between TF and its binding site. The whole tree-structured PWM could be considered as a mixture of different conditional-PWMs. We propose a discriminative approach, called TPD (TPWM based Discriminative Approach), to construct the TPWM from the ChIP-Seq data with a pre-existing PWM. To achieve the maximum discriminative power between the positive and negative datasets, the cutoff value is determined based on the Matthew Correlation Coefficient (MCC). The resulting TPWMs are evaluated with respect to accuracy on extensive synthetic datasets. We then apply our TPWM discriminative approach on several real ChIP-Seq datasets to refine the current TFBS models stored in the TRANSFAC database. Experiments on both the simulated and real ChIP-Seq data show that the proposed method starting from existing PWM has consistently better performance than existing tools in detecting the TFBSs. The improved accuracy is the result of modelling the complete dependent structure of the motifs and better prediction of true positive rate. The findings could lead to better understanding of the mechanisms of TF-DNA interactions. Public Library of Science 2011-09-02 /pmc/articles/PMC3166302/ /pubmed/21912677 http://dx.doi.org/10.1371/journal.pone.0024210 Text en Bi et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Bi, Yingtao Kim, Hyunsoo Gupta, Ravi Davuluri, Ramana V. Tree-Based Position Weight Matrix Approach to Model Transcription Factor Binding Site Profiles |
title | Tree-Based Position Weight Matrix Approach to Model Transcription Factor Binding Site Profiles |
title_full | Tree-Based Position Weight Matrix Approach to Model Transcription Factor Binding Site Profiles |
title_fullStr | Tree-Based Position Weight Matrix Approach to Model Transcription Factor Binding Site Profiles |
title_full_unstemmed | Tree-Based Position Weight Matrix Approach to Model Transcription Factor Binding Site Profiles |
title_short | Tree-Based Position Weight Matrix Approach to Model Transcription Factor Binding Site Profiles |
title_sort | tree-based position weight matrix approach to model transcription factor binding site profiles |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166302/ https://www.ncbi.nlm.nih.gov/pubmed/21912677 http://dx.doi.org/10.1371/journal.pone.0024210 |
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