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QChIPat: a quantitative method to identify distinct binding patterns for two biological ChIP-seq samples in different experimental conditions

机译:QChIPat:一种定量方法,可在不同的实验条件下鉴定两种生物ChIP-seq样品的独特结合模式

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BackgroundMany computational programs have been developed to identify enriched regions for a single biological ChIP-seq sample. Given that many biological questions are often asked to compare the difference between two different conditions, it is important to develop new programs that address the comparison of two biological ChIP-seq samples. Despite several programs designed to address this question, these programs suffer from some drawbacks, such as inability to distinguish whether the identified differential enriched regions are indeed significantly enriched, lack of distinguishing binding patterns, and neglect of the normalization between samples.ResultsIn this study, we developed a novel quantitative method for comparing two biological ChIP-seq samples, called QChIPat. Our method employs a new global normalization method: nonparametric empirical Bayes (NEB) correction normalization, utilizes pre-defined enriched regions identified from single-sample peak calling programs, uses statistical methods to define differential enriched regions, then defines binding (histone modification) pattern information for those differential enriched regions. Our program was tested on a benchmark data: histone modifications data used by ChIPDiffs. It was then applied on two study cases: one to identify differential histone modification sites for ChIP-seq of H3K27me3 and H3K9me2 data in AKT1-transfected MCF10A cells; the other to identify differential binding sites for ChIP-seq of TCF7L2 data in MCF7 and PANC1 cells.ConclusionsSeveral advantages of our program include: 1) it considers a control (or input) experiment; 2) it incorporates a novel global normalization strategy: nonparametric empirical Bayes correction normalization; 3) it provides the binding pattern information among different enriched regions. QChIPat is implemented in R, Perl and C++, and has been tested under Linux. The R package is available at http://motif.bmi.ohio-state.edu/QChIPat.
机译:背景技术已经开发了许多计算程序来识别单个生物ChIP-seq样品的富集区域。鉴于经常需要回答许多生物学问题来比较两种不同条件之间的差异,因此开发新的程序以解决两种生物学ChIP-seq样品的比较问题非常重要。尽管设计了多个程序来解决此问题,但这些程序仍存在一些缺陷,例如无法区分所识别的差异富集区域是否确实显着富集,缺乏独特的结合模式以及样品之间的归一化方法被忽略。我们开发了一种新颖的定量方法,用于比较两个生物ChIP-seq样品,称为QChIPat。我们的方法采用了一种新的全局归一化方法:非参数经验贝叶斯(NEB)校正归一化,利用了从单样本峰调用程序中识别出的预定义的富集区域,使用统计方法来定义差分富集区域,然后定义了绑定(组蛋白修饰)模式这些差异丰富区域的信息。我们的程序在基准数据上进行了测试:ChIPDiffs使用的组蛋白修饰数据。然后将其应用于两个研究案例:一个用于识别AKT1转染的MCF10A细胞中H3K27me3和H3K9me2数据的ChIP-seq差异组蛋白修饰位点;结论我们程序的几个优点包括:1)考虑了一个对照(或输入)实验;另外,它还确定了MCF7和PANC1细胞中TCF7L2数据ChIP-seq的差异结合位点。 2)它结合了一种新颖的全局归一化策略:非参数经验贝叶斯校正归一化; 3)它提供了不同富集区域之间的绑定模式信息。 QChIPat在R,Perl和C ++中实现,并已在Linux下进行了测试。 R包可从http://motif.bmi.ohio-state.edu/QChIPat获得。

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