Sequence2Vec: A novel embedding approach for modeling transcription factor binding affinity landscape
KAUST DepartmentComputational Bioscience Research Center (CBRC)
Computer, Electrical and Mathematical Sciences and Engineering (CEMSE) Division
Permanent link to this recordhttp://hdl.handle.net/10754/625301
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AbstractMotivation: 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 (HMM) 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 HMMs 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 data sets 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.
CitationDai H, Umarov R, Kuwahara H, Li Y, Song L, et al. (2017) Sequence2Vec: A novel embedding approach for modeling transcription factor binding affinity landscape. Bioinformatics. Available: http://dx.doi.org/10.1093/bioinformatics/btx480.
SponsorsThe research reported in this publication was supported by the King Abdullah University of Science and Technology (KAUST) Office of Sponsored Research (OSR) under Award No. URF/1/1976-04 and URF/1/3007-01. It was also supported in part by NSF IIS-1218749, NIH BIGDATA 1R01GM108341, NSF CAREER IIS-1350983, NSF IIS-1639792 EAGER, ONR N00014-15-1-2340, NVIDIA, Intel and Amazon AWS. This research made use of the resources of the computer clusters at KAUST.
PublisherOxford University Press (OUP)
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