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iASeq: integrative analysis of allele-specificity of protein-DNA interactions in multiple ChIP-seq datasets

机译:iASeq:在多个ChIP-seq数据集中蛋白质-DNA相互作用的等位基因特异性的综合分析

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Background ChIP-seq provides new opportunities to study allele-specific protein-DNA binding (ASB). However, detecting allelic imbalance from a single ChIP-seq dataset often has low statistical power since only sequence reads mapped to heterozygote SNPs are informative for discriminating two alleles. Results We develop a new method iASeq to address this issue by jointly analyzing multiple ChIP-seq datasets. iASeq uses a Bayesian hierarchical mixture model to learn correlation patterns of allele-specificity among multiple proteins. Using the discovered correlation patterns, the model allows one to borrow information across datasets to improve detection of allelic imbalance. Application of iASeq to 77 ChIP-seq samples from 40 ENCODE datasets and 1 genomic DNA sample in GM12878 cells reveals that allele-specificity of multiple proteins are highly correlated, and demonstrates the ability of iASeq to improve allelic inference compared to analyzing each individual dataset separately. Conclusions iASeq illustrates the value of integrating multiple datasets in the allele-specificity inference and offers a new tool to better analyze ASB.
机译:背景ChIP-seq提供了研究等位基因特异性蛋白质-DNA结合(ASB)的新机会。但是,从单个ChIP-seq数据集中检测等位基因失衡通常具有较低的统计能力,因为只有映射到杂合子SNP的序列读数才有助于区分两个等位基因。结果我们通过联合分析多个ChIP-seq数据集开发了一种新的iASeq方法来解决此问题。 iASeq使用贝叶斯分层混合模型来了解多种蛋白质之间等位基因特异性的相关模式。使用发现的相关模式,该模型允许人们跨数据集借阅信息,以改善对等位基因失衡的检测。将iASeq应用于GM12878细胞中40个ENCODE数据集和1个基因组DNA样品中的77个ChIP-seq样品中,揭示了多种蛋白质的等位基因特异性高度相关,并证明了iASeq改善等位基因推断的能力(与分别分析每个单独的数据集相比) 。结论iASeq在等位基因特异性推断中说明了整合多个数据集的价值,并提供了更好地分析ASB的新工具。

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