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dc.contributor.advisorZhang, Michael Q., Xing, Haipengen_US
dc.contributor.authorMo, Yifanen_US
dc.contributor.otherDepartment of Applied Mathematics and Statisticsen_US
dc.date.accessioned2013-05-22T17:35:17Z
dc.date.available2013-05-22T17:35:17Z
dc.date.issued1-Dec-12en_US
dc.date.submitted12-Decen_US
dc.identifierMo_grad.sunysb_0771E_11168en_US
dc.identifier.urihttp://hdl.handle.net/1951/59794
dc.description107 pg.en_US
dc.description.abstractNowadays, Hidden Markov Model (HMM) has been widely used in analysis of various biological data for both smoothing and clustering. However, characterizing each hidden state by a single distribution, the classical HMM might have some limitations on the data whose hidden state is composed by a mixture of distributions (Heng Lian et al., 2006). To address this issue, we proposed a new stochastic segmentation model and an associated estimation procedure that has attractive analytical and computational properties. We combined the forward and backward filter together based on Bayes' theorem to calculate the posterior mean and variance. Besides, we developed an expectation-maximization (EM) algorithm to estimate the hyper-parameters. Furthermore, we utilized a bounded complexity mixture (BCMIX) approximation whose computational complexity is linear in sequence length. Another important feature of this segmentation model is that it yields explicit formulas for posterior means and probability of categorical states, which can be used to make inference on both categorical and continuous aspects of the data. Other quantities relating to the posterior distribution that are useful for making confidence assessments of any given segmentation can also be estimated by using our method. We perform intensive simulation studies (1) to compare the Bayes and BCMIX estimates (2) to evaluate the BCMIX estimates in terms of sum square error, Kullback-Leibler divergence and the identification ratio of true segments. We also applied our model on two biological data sets: (1) reduced representation bisulfite sequencing (RRBS) data (A.Molaro et al., 2011) (2) ENCODE Nimblegen tilled arrays (Sabo et al., 2006). Our model shows good performance on segmentation of these two sequential data. In RRBS data it can further help identify differential methylation region (DMR) while in microarray data it can discover the DNAsel Hypersensitive Sites (DHSs).en_US
dc.description.sponsorshipStony Brook University Libraries. SBU Graduate School in Department of Applied Mathematics and Statistics. Charles Taber (Dean of Graduate School).en_US
dc.formatElectronic Resourceen_US
dc.language.isoen_USen_US
dc.publisherThe Graduate School, Stony Brook University: Stony Brook, NY.en_US
dc.subject.lcshStatisticsen_US
dc.titleA Stochastic Segmentation Model for Categorical and Continuous Features of various biological sequentialen_US
dc.typeDissertationen_US
dc.description.advisorAdvisor(s): Zhang, Michael Q.Xing, Haipeng. Committee Member(s): Wu, Song ; Fang, Yixin.en_US
dc.mimetypeApplication/PDFen_US


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