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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 13: Finding RNA–Protein Interaction Sites Using HMMs
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Chapter title
Finding RNA–Protein Interaction Sites Using HMMs
Chapter number 13
Book title
Hidden Markov Models
Published in
Methods in molecular biology, February 2017
DOI 10.1007/978-1-4939-6753-7_13
Pubmed ID
Book ISBNs
978-1-4939-6751-3, 978-1-4939-6753-7
Authors

Tao Wang, Jonghyun Yun, Yang Xie, Guanghua Xiao

Editors

David R. Westhead, M. S. Vijayabaskar

Abstract

RNA-binding proteins play important roles in the various stages of RNA maturation through binding to its target RNAs. Cross-linking immunoprecipitation coupled with high-throughput sequencing (CLIP-Seq) has made it possible to identify the targeting sites of RNA-binding proteins in various cell culture systems and tissue types on a genome-wide scale. Several Hidden Markov model-based (HMM) approaches have been suggested to identify protein-RNA binding sites from CLIP-Seq datasets. In this chapter, we describe how HMM can be applied to analyze CLIP-Seq datasets, including the bioinformatics preprocessing steps to extract count information from the sequencing data before HMM and the downstream analysis steps following peak-calling.

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Mendeley readers

The data shown below were compiled from readership statistics for 2 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 2 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 50%
Unknown 1 50%
Readers by discipline Count As %
Medicine and Dentistry 1 50%
Unknown 1 50%