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Sequence2Vec: a novel embedding approach for modeling transcription factor binding affinity landscape
MOTIVATION: An accurate characterization of transcription factor (TF)-DNA affinity landscape is crucial to a quantitative understanding of the molecular mechanisms underpinning endogenous gene regulation. While recent advances in biotechnology have brought the opportunity for building binding affini...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870668/ https://www.ncbi.nlm.nih.gov/pubmed/28961686 http://dx.doi.org/10.1093/bioinformatics/btx480 |
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author | Dai, Hanjun Umarov, Ramzan Kuwahara, Hiroyuki Li, Yu Song, Le Gao, Xin |
author_facet | Dai, Hanjun Umarov, Ramzan Kuwahara, Hiroyuki Li, Yu Song, Le Gao, Xin |
author_sort | Dai, Hanjun |
collection | PubMed |
description | MOTIVATION: An accurate characterization of transcription factor (TF)-DNA affinity landscape is crucial to a quantitative understanding of the molecular mechanisms underpinning endogenous gene regulation. While recent advances in biotechnology have brought the opportunity for building binding affinity prediction methods, the accurate characterization of TF-DNA binding affinity landscape still remains a challenging problem. RESULTS: Here we propose a novel sequence embedding approach for modeling the transcription factor binding affinity landscape. Our method represents DNA binding sequences as a hidden Markov model which captures both position specific information and long-range dependency in the sequence. A cornerstone of our method is a novel message passing-like embedding algorithm, called Sequence2Vec, which maps these hidden Markov models into a common nonlinear feature space and uses these embedded features to build a predictive model. Our method is a novel combination of the strength of probabilistic graphical models, feature space embedding and deep learning. We conducted comprehensive experiments on over 90 large-scale TF-DNA datasets which were measured by different high-throughput experimental technologies. Sequence2Vec outperforms alternative machine learning methods as well as the state-of-the-art binding affinity prediction methods. AVAILABILITY AND IMPLEMENTATION: Our program is freely available at https://github.com/ramzan1990/sequence2vec. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. |
format | Online Article Text |
id | pubmed-5870668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-58706682018-04-05 Sequence2Vec: a novel embedding approach for modeling transcription factor binding affinity landscape Dai, Hanjun Umarov, Ramzan Kuwahara, Hiroyuki Li, Yu Song, Le Gao, Xin Bioinformatics Original Papers MOTIVATION: An accurate characterization of transcription factor (TF)-DNA affinity landscape is crucial to a quantitative understanding of the molecular mechanisms underpinning endogenous gene regulation. While recent advances in biotechnology have brought the opportunity for building binding affinity prediction methods, the accurate characterization of TF-DNA binding affinity landscape still remains a challenging problem. RESULTS: Here we propose a novel sequence embedding approach for modeling the transcription factor binding affinity landscape. Our method represents DNA binding sequences as a hidden Markov model which captures both position specific information and long-range dependency in the sequence. A cornerstone of our method is a novel message passing-like embedding algorithm, called Sequence2Vec, which maps these hidden Markov models into a common nonlinear feature space and uses these embedded features to build a predictive model. Our method is a novel combination of the strength of probabilistic graphical models, feature space embedding and deep learning. We conducted comprehensive experiments on over 90 large-scale TF-DNA datasets which were measured by different high-throughput experimental technologies. Sequence2Vec outperforms alternative machine learning methods as well as the state-of-the-art binding affinity prediction methods. AVAILABILITY AND IMPLEMENTATION: Our program is freely available at https://github.com/ramzan1990/sequence2vec. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Oxford University Press 2017-11-15 2017-07-27 /pmc/articles/PMC5870668/ /pubmed/28961686 http://dx.doi.org/10.1093/bioinformatics/btx480 Text en © The Author 2017. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Papers Dai, Hanjun Umarov, Ramzan Kuwahara, Hiroyuki Li, Yu Song, Le Gao, Xin Sequence2Vec: a novel embedding approach for modeling transcription factor binding affinity landscape |
title | Sequence2Vec: a novel embedding approach for modeling transcription factor binding affinity landscape |
title_full | Sequence2Vec: a novel embedding approach for modeling transcription factor binding affinity landscape |
title_fullStr | Sequence2Vec: a novel embedding approach for modeling transcription factor binding affinity landscape |
title_full_unstemmed | Sequence2Vec: a novel embedding approach for modeling transcription factor binding affinity landscape |
title_short | Sequence2Vec: a novel embedding approach for modeling transcription factor binding affinity landscape |
title_sort | sequence2vec: a novel embedding approach for modeling transcription factor binding affinity landscape |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5870668/ https://www.ncbi.nlm.nih.gov/pubmed/28961686 http://dx.doi.org/10.1093/bioinformatics/btx480 |
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