PolyaPeak: Detecting Transcription Factor Binding Sites from ChIP-seq Using Peak Shape Information

被引:10
|
作者
Wu, Hao [1 ]
Ji, Hongkai [2 ]
机构
[1] Emory Univ, Dept Biostat & Bioinformat, Atlanta, GA 30322 USA
[2] Johns Hopkins Univ, Dept Biostat, Baltimore, MD 21205 USA
来源
PLOS ONE | 2014年 / 9卷 / 03期
关键词
GENOME; IDENTIFICATION; PROFILES;
D O I
10.1371/journal.pone.0089694
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
ChIP-seq is a powerful technology for detecting genomic regions where a protein of interest interacts with DNA. ChIP-seq data for mapping transcription factor binding sites (TFBSs) have a characteristic pattern: around each binding site, sequence reads aligned to the forward and reverse strands of the reference genome form two separate peaks shifted away from each other, and the true binding site is located in between these two peaks. While it has been shown previously that the accuracy and resolution of binding site detection can be improved by modeling the pattern, efficient methods are unavailable to fully utilize that information in TFBS detection procedure. We present PolyaPeak, a new method to improve TFBS detection by incorporating the peak shape information. PolyaPeak describes peak shapes using a flexible Polya model. The shapes are automatically learnt from the data using Minorization-Maximization (MM) algorithm, then integrated with the read count information via a hierarchical model to distinguish true binding sites from background noises. Extensive real data analyses show that PolyaPeak is capable of robustly improving TFBS detection compared with existing methods. An R package is freely available.
引用
收藏
页数:9
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