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Detecting DNA Modifications from SMRT Sequencing Data by Modeling Sequence Context Dependence of Polymerase Kinetic

机译:通过建模序列上下文依赖聚合酶动力学从SMRT测序数据中检测DNA修饰。

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摘要

DNA modifications such as methylation and DNA damage can play critical regulatory roles in biological systems. Single molecule, real time (SMRT) sequencing technology generates DNA sequences as well as DNA polymerase kinetic information that can be used for the direct detection of DNA modifications. We demonstrate that local sequence context has a strong impact on DNA polymerase kinetics in the neighborhood of the incorporation site during the DNA synthesis reaction, allowing for the possibility of estimating the expected kinetic rate of the enzyme at the incorporation site using kinetic rate information collected from existing SMRT sequencing data (historical data) covering the same local sequence contexts of interest. We develop an Empirical Bayesian hierarchical model for incorporating historical data. Our results show that the model could greatly increase DNA modification detection accuracy, and reduce requirement of control data coverage. For some DNA modifications that have a strong signal, a control sample is not even needed by using historical data as alternative to control. Thus, sequencing costs can be greatly reduced by using the model. We implemented the model in a R package named seqPatch, which is available at .
机译:DNA修饰(例如甲基化和DNA损伤)可以在生物系统中发挥关键的调节作用。单分子实时(SMRT)测序技术可生成DNA序列以及DNA聚合酶动力学信息,可用于直接检测DNA修饰。我们证明本地序列上下文对DNA合成反应过程中掺入位点附近的DNA聚合酶动力学有很强的影响,允许使用从收集到的动力学速率信息估算掺入位点的酶的预期动力学速率。现有的SMRT测序数据(历史数据)覆盖了感兴趣的相同局部序列上下文。我们开发了经验贝叶斯分层模型来合并历史数据。我们的结果表明该模型可以大大提高DNA修饰检测的准确性,并减少对控制数据覆盖的要求。对于某些具有强烈信号的DNA修饰,甚至不需要使用历史数据作为对照的对照样品。因此,使用该模型可以大大降低测序成本。我们在名为seqPatch的R包中实现了该模型,该包可在处获得。

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