4.7 Article

HEPeak: an HMM-based exome peak-finding package for RNA epigenome sequencing data

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BMC GENOMICS
卷 16, 期 -, 页码 -

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BIOMED CENTRAL LTD
DOI: 10.1186/1471-2164-16-S4-S2

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  1. National Institute on Minority Health and Health Disparities from the National Institutes of Health [G12MD007591]
  2. National Institutes of Health [NIH-NCIP30CA54174]
  3. National Science Foundation [CCF-0546345]
  4. Qatar National Research Fund [09-874-3-235]
  5. William and Ella Medical Research Foundation
  6. Thrive Well Foundation
  7. Max and Minnie Tomerlin Voelcker Fund
  8. Direct For Computer & Info Scie & Enginr
  9. Division of Computing and Communication Foundations [1246073] Funding Source: National Science Foundation

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Background: Methylated RNA Immunoprecipatation combined with RNA sequencing (MeRIP-seq) is revolutionizing the de novo study of RNA epigenomics at a higher resolution. However, this new technology poses unique bioinformatics problems that call for novel and sophisticated statistical computational solutions, aiming at identifying and characterizing transcriptome-wide methyltranscriptome. Results: We developed HEP, a Hidden Markov Model (HMM)-based Exome Peak-finding algorithm for predicting transcriptome methylation sites using MeRIP-seq data. In contrast to exomePeak, our previously developed MeRIP-seq peak calling algorithm, HEPeak models the correlation between continuous bins in an m(6)A peak region and it is a model-based approach, which admits rigorous statistical inference. HEPeak was evaluated on a simulated MeRIP-seq dataset and achieved higher sensitivity and specificity than exomePeak. HEPeak was also applied to real MeRIP-seq datasets from human HEK293T cell line and mouse midbrain cells and was shown to be able to recapitulate known m(6)A distribution in transcripts and identify novel m6A sites in long non-coding RNAs. Conclusions: In this paper, a novel HMM-based peak calling algorithm, HEPeak, was developed for peak calling for MeRIP-seq data. HEPeak is written in R and is publicly available.

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