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|Title:||An HMM approach to genome-wide identification of differential histone modification sites from ChIP-seq data|
|Citation:||Xu, H., Wei, C.-L., Lin, F., Sung, W.-K. (2008). An HMM approach to genome-wide identification of differential histone modification sites from ChIP-seq data. Bioinformatics 24 (20) : 2344-2349. ScholarBank@NUS Repository. https://doi.org/10.1093/bioinformatics/btn402|
|Abstract:||Motivation: Epigenetic modifications are one of the critical factors to regulate gene expression and genome function. Among different epigenetic modifications, the differential histone modification sites (DHMSs) are of great interest to study the dynamic nature of epigenetic and gene expression regulations among various cell types, stages or environmental responses. To capture the histone modifications at whole genome scale, ChIP-seq technology is becoming a robust and comprehensive approach. Thus the DHMSs are potentially identifiable by comparing two ChIP-seq libraries. However, little has been addressed on this issue in literature. Results: Aiming at identifying DHMSs, we propose an approach called ChIPDiff for the genome-wide comparison of histone modification sites identified by ChIP-seq. Based on the observations of ChIP fragment counts, the proposed approach employs a hidden Markov model (HMM) to infer the states of histone modification changes at each genomic location. We evaluated the performance of ChIPDiff by comparing the H3K27me3 modification sites between mouse embryonic stem cell (ESC) and neural progenitor cell (NPC). We demonstrated that the H3K27me3 DHMSs identified by our approach are of high sensitivity, specificity and technical reproducibility. ChIPDiff was further applied to uncover the differential H3K4me3 and H3K36me3 sites between different cell states. Interesting biological discoveries were achieved from such comparison in our study. © The Author 2008. Published by Oxford University Press. All rights reserved.|
|Appears in Collections:||Staff Publications|
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