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A Review of Three Different Studies on Hidden Markov Models for Epigenetic Problems: A Computational Perspective

机译:基于表观遗传问题的隐马尔可夫模型的三项不同研究综述:一种计算视角

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摘要

Recent technical advances, such as chromatin immunoprecipitation combined with DNA microarrays (ChIp-chip) and chromatin immunoprecipitation-sequencing (ChIP-seq), have generated large quantities of high-throughput data. Considering that epigenomic datasets are arranged over chromosomes, their analysis must account for spatial or temporal characteristics. In that sense, simple clustering or classification methodologies are inadequate for the analysis of multi-track ChIP-chip or ChIP-seq data. Approaches that are based on hidden Markov models (HMMs) can integrate dependencies between directly adjacent measurements in the genome. Here, we review three HMM-based studies that have contributed to epigenetic research, from a computational perspective. We also give a brief tutorial on HMM modelling-targeted at bioinformaticians who are new to the field.
机译:最近的技术进步,例如结合DNA微阵列的染色质免疫沉淀(ChIp芯片)和染色质免疫沉淀测序(ChIP-seq),已经产生了大量的高通量数据。考虑到表观基因组数据集排列在染色体上,其分析必须考虑空间或时间特征。从这个意义上说,简单的聚类或分类方法不足以分析多轨道ChIP芯片或ChIP-seq数据。基于隐马尔可夫模型(HMM)的方法可以整合基因组中直接相邻测量之间的依赖性。在这里,我们从计算的角度回顾了三项基于HMM的研究,这些研究为表观遗传学研究做出了贡献。我们还针对针对该领域的生物信息学家提供了有关HMM建模的简短教程。

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