Computation-Based Discovery of Cis-Regulatory Modules by Hidden Markov Model. Export

@article{citeulike:2529422, abstract = {A key component in genome sequence analysis is the identification of regions of the genome that contain regulatory information. In higher eukaryotes, this information is organized into modular units called cis-regulatory modules. Each module contains multiple binding sites for a specific combination of several transcription factors. In this article, we propose a hidden Markov model (HMM) to identify transcription factor binding sites (TFBSs) and cis-regulatory modules (CRMs). For a given genomic sequence, we first select potential TFBSs from a large database (e.g., TRANSFAC), then construct an HMM where the TFBSs are only counted when they occur within a specialized CRM state. The novel features of the proposed method include that it does not assume a small set of TFBSs for a given gene; on the other hand, the method utilizes information from a large collection of well-characterized TFBSs and therefore is computationally more efficient and robust than the de novo methods. Our approach is applied to three data sets with experimentally evaluated TFBSs. The method shows better specificity and sensitivity than other similar computational tools in identifying CRMs and TFBSs. The executable codes of our programs and module predictions across the fly Drosophila genome are available at www.stat.purdue.edu/ approximately jingwu/module/.}, address = {Department of Statistics, Purdue University, West Lafayette, Indiana, 47907.}, author = {Wu, Jing and Xie, Jun}, citeulike-article-id = {2529422}, citeulike-linkout-0 = {http://dx.doi.org/10.1089/cmb.2008.0024}, citeulike-linkout-1 = {http://view.ncbi.nlm.nih.gov/pubmed/18333759}, citeulike-linkout-2 = {http://www.hubmed.org/display.cgi?uids=18333759}, day = {11}, doi = {10.1089/cmb.2008.0024}, issn = {1066-5277}, journal = {J Comput Biol}, keywords = {cis-regulatory-element, hidden-markov-models, hmms, tfbs, transcription-factor}, month = {March}, posted-at = {2009-06-19 13:27:13}, priority = {3}, title = {Computation-Based Discovery of Cis-Regulatory Modules by Hidden Markov Model.}, url = {http://dx.doi.org/10.1089/cmb.2008.0024}, year = {2008} }

TY - JOUR ID - citeulike:2529422 L3 - citeulike-article-id:2529422 N2 - A key component in genome sequence analysis is the identification of regions of the genome that contain regulatory information. In higher eukaryotes, this information is organized into modular units called cis-regulatory modules. Each module contains multiple binding sites for a specific combination of several transcription factors. In this article, we propose a hidden Markov model (HMM) to identify transcription factor binding sites (TFBSs) and cis-regulatory modules (CRMs). For a given genomic sequence, we first select potential TFBSs from a large database (e.g., TRANSFAC), then construct an HMM where the TFBSs are only counted when they occur within a specialized CRM state. The novel features of the proposed method include that it does not assume a small set of TFBSs for a given gene; on the other hand, the method utilizes information from a large collection of well-characterized TFBSs and therefore is computationally more efficient and robust than the de novo methods. Our approach is applied to three data sets with experimentally evaluated TFBSs. The method shows better specificity and sensitivity than other similar computational tools in identifying CRMs and TFBSs. The executable codes of our programs and module predictions across the fly Drosophila genome are available at www.stat.purdue.edu/ approximately jingwu/module/. JF - J Comput Biol SN - 1066-5277 AD - Department of Statistics, Purdue University, West Lafayette, Indiana, 47907. TI - Computation-Based Discovery of Cis-Regulatory Modules by Hidden Markov Model. KW - cis-regulatory-element KW - hidden-markov-models KW - hmms KW - tfbs KW - transcription-factor AU - Wu, Jing AU - Xie, Jun PY - 2008/03/11/ UR - http://dx.doi.org/10.1089/cmb.2008.0024 ER -