A STATISTICAL MODEL TO ASSESS (ALLELE-SPECIFIC) ASSOCIATIONS BETWEEN GENE EXPRESSION AND EPIGENETIC FEATURES USING SEQUENCING DATA

• 成果类型: Article
• 署名作者: Rashid, Naim U.; Sun, Wei; Ibrahim, Joseph G.
• 署名单位: University of North Carolina; University of North Carolina Chapel Hill; Fred Hutchinson Cancer Center
• 刊物名称: ANNALS OF APPLIED STATISTICS
• ISSN/ISSBN: 1932-6157
• DOI: 10.1214/16-AOAS973
• 发表日期: 2016
• 页码: 2254-2273
• 关键词: chromatin; landscape; transcription; sensitivity

摘要

Sequencing techniques have been widely used to assess gene expression (i.e., RNA-seq) or the presence of epigenetic features (e.g., DNase-seq to identify open chromatin regions). In contrast to traditional microarray platforms, sequencing data are typically summarized in the form of discrete counts, and they are able to delineate allele-specific signals, which are not available from microarrays. The presence of epigenetic features are often associated with gene expression, both of which have been shown to be affected by DNA polymorphisms. However, joint models with the flexibility to assess interactions between gene expression, epigenetic features and DNA polymorphisms are currently lacking. In this paper, we develop a statistical model to assess the associations between gene expression and epigenetic features using sequencing data, while explicitly modeling the effects of DNA polymorphisms in either an allele-specific or nonallele-specific manner. We show that in doing so we provide the flexibility to detect associations between gene expression and epigenetic features, as well as conditional associations given DNA polymorphisms. We evaluate the performance of our method using simulations and apply our method to study the association between gene expression and the presence of DNase I Hypersensitive sites (DHSs) in HapMap individuals. Our model can be generalized to exploring the relationships between DNA polymorphisms and any two types of sequencing experiments, a useful feature as the variety of sequencing experiments continue to expand.