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Ancestral transcriptome inference based on RNA-Seq and ChIP-seq data

机译:基于RNA-SEQ和CHIP-SEQ数据的祖先转录组推断

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摘要

With the help of high-throughput NGS (next-generation sequencing) technologies, ancestral transcriptome reconstruction is helpful to understand the complexity of transcriptional regulatory systems that underlies the evolution of multiple cellular metazoans with sophisticated functions and distinctive morphologies. To this end, we report a new method of ancestral state inference. The new method used Ornstein-Uhlenbeck (OU) model, which is more biologically realistic, to replace the Brownian motion (BM) model and is suitable for multi-transcriptome data. Implemented in the free R package, AnceTran is specially designed for RNA-seq and ChIP-seq data, which is feasible. It should be noticed that our work will be integrated to a unified, statistically-sound phylogenetic framework to study the evolution of many other molecular phenomes such as proteomics, chromatin accessibility, methylation status, and metabolomics. We exemplify our method by a case study, using the ChIP-seq binding data of three liver-specific transcription factors and the RNA-seq liver expression data in four closely related mice species, and some technical issues are discussed.
机译:在高通量NGS(下一代测序)技术的帮助下,祖先的转录组重建是有助于了解转录调节系统的复杂性,这些系统的复杂性化细胞化美唑烷具有复杂功能和独特形态的演变。为此,我们报告了一种新的祖先国家推断方法。使用ornstein-uhlenbeck(OU)模型的新方法,更具生物学逼真,更换布朗运动(BM)模型,适用于多转录组数据。在Free R包中实施,Ancetran专为RNA-SEQ和Chip-SEQ数据而设计,这是可行的。应该注意的是,我们的作品将被整合到统一的统计声音发育框架,以研究许多其他分子表的演变,例如蛋白质组学,染色质可用性,甲基化状态和代谢组。我们通过案例研究举例说明了我们的方法,使用三个肝脏特异性转录因子的芯片-SEQ结合数据和四个密切相关的小鼠物种中的RNA-SEQ肝脏表达数据,并讨论了一些技术问题。

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