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Hidden Markov Models

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Cover of 'Hidden Markov Models'

Table of Contents

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    Book Overview
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    Chapter 1 Introduction to Hidden Markov Models and Its Applications in Biology
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    Chapter 2 HMMs in Protein Fold Classification
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    Chapter 3 Application of Hidden Markov Models in Biomolecular Simulations
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    Chapter 4 Predicting Beta Barrel Transmembrane Proteins Using HMMs
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    Chapter 5 Predicting Alpha Helical Transmembrane Proteins Using HMMs
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    Chapter 6 Self-Organizing Hidden Markov Model Map (SOHMMM): Biological Sequence Clustering and Cluster Visualization
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    Chapter 7 Analyzing Single Molecule FRET Trajectories Using HMM
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    Chapter 8 Modelling ChIP-seq Data Using HMMs
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    Chapter 9 Hidden Markov Models in Bioinformatics: SNV Inference from Next Generation Sequence
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    Chapter 10 Computationally Tractable Multivariate HMM in Genome-Wide Mapping Studies
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    Chapter 11 Hidden Markov Models in Population Genomics
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    Chapter 12 Differential Gene Expression (DEX) and Alternative Splicing Events (ASE) for Temporal Dynamic Processes Using HMMs and Hierarchical Bayesian Modeling Approaches
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    Chapter 13 Finding RNA–Protein Interaction Sites Using HMMs
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    Chapter 14 Automated Estimation of Mouse Social Behaviors Based on a Hidden Markov Model
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    Chapter 15 Modeling Movement Primitives with Hidden Markov Models for Robotic and Biomedical Applications
Attention for Chapter 10: Computationally Tractable Multivariate HMM in Genome-Wide Mapping Studies
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Chapter title
Computationally Tractable Multivariate HMM in Genome-Wide Mapping Studies
Chapter number 10
Book title
Hidden Markov Models
Published in
Methods in molecular biology, February 2017
DOI 10.1007/978-1-4939-6753-7_10
Pubmed ID
Book ISBNs
978-1-4939-6751-3, 978-1-4939-6753-7
Authors

Hyungwon Choi, Debashis Ghosh, Zhaohui Qin

Editors

David R. Westhead, M. S. Vijayabaskar

Abstract

Hidden Markov model (HMM) is widely used for modeling spatially correlated genomic data (series data). In genomics, datasets of this kind are generated from genome-wide mapping studies through high-throughput methods such as chromatin immunoprecipitation coupled with massively parallel sequencing (ChIP-seq). When multiple regulatory protein binding sites or related epigenetic modifications are mapped simultaneously, the correlation between data series can be incorporated into the latent variable inference in a multivariate form of HMM, potentially increasing the statistical power of signal detection. In this chapter, we review the challenges of multivariate HMMs and propose a computationally tractable method called sparsely correlated HMMs (scHMM). We illustrate the method and the scHMM package using an example mouse ChIP-seq dataset.

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Mendeley readers

The data shown below were compiled from readership statistics for 3 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 3 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 2 67%
Unknown 1 33%
Readers by discipline Count As %
Social Sciences 1 33%
Neuroscience 1 33%
Unknown 1 33%