Spatially Enhanced Differential RNA Methylation Analysis from Affinity-Based Sequencing Data with Hidden Markov Model.

With the development of new sequencing technology, the entire N6-methyl-adenosine (m(6)A) RNA methylome can now be unbiased profiled with methylated RNA immune-precipitation sequencing technique (MeRIP-Seq), making it possible to detect differential methylation states of RNA between two conditions,...

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Publicado en:BioMed Research International Vol. 2015; pp. 1 - 13
Autores principales: Zhang, Yu-Chen, Zhang, Shao-Wu, Liu, Lian, Liu, Hui, Zhang, Lin, Cui, Xiaodong, Huang, Yufei, Meng, Jia
Formato: equations & formulas research tables/charts Journal Article
Publicado: Wiley-Blackwell 8/2/2015
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 8/2/2015
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2015/852070
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        atl: Spatially Enhanced Differential RNA Methylation Analysis from Affinity-Based Sequencing Data with Hidden Markov Model.
      aug:
        au:
          Zhang, Yu-Chen
          Zhang, Shao-Wu
          Liu, Lian
          Liu, Hui
          Zhang, Lin
          Cui, Xiaodong
          Huang, Yufei
          Meng, Jia
        affil: Key Laboratory of Information Fusion Technology of Ministry of Education, School of Automation, Northwestern Polytechnical University, Xi’an 710072, China
      sug:
        subj:
          Methylation Evaluation
          RNA
          Neoplasms Diagnosis
          Hidden Markov Models
          Human
          Funding Source
          China
          Academic Medical Centers
          Fisher's Exact Test
      ab: With the development of new sequencing technology, the entire N6-methyl-adenosine (m(6)A) RNA methylome can now be unbiased profiled with methylated RNA immune-precipitation sequencing technique (MeRIP-Seq), making it possible to detect differential methylation states of RNA between two conditions, for example, between normal and cancerous tissue. However, as an affinity-based method, MeRIP-Seq has yet provided base-pair resolution; that is, a single methylation site determined from MeRIP-Seq data can in practice contain multiple RNA methylation residuals, some of which can be regulated by different enzymes and thus differentially methylated between two conditions. Since existing peak-based methods could not effectively differentiate multiple methylation residuals located within a single methylation site, we propose a hidden Markov model (HMM) based approach to address this issue. Specifically, the detected RNA methylation site is further divided into multiple adjacent small bins and then scanned with higher resolution using a hidden Markov model to model the dependency between spatially adjacent bins for improved accuracy. We tested the proposed algorithm on both simulated data and real data. Result suggests that the proposed algorithm clearly outperforms existing peak-based approach on simulated systems and detects differential methylation regions with higher statistical significance on real dataset.
      pubtype: Academic Journal
      doctype:
        equations & formulas
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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