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NONPARAMETRIC BAYESIAN LEARNING OF HETEROGENEOUS DYNAMIC TRANSCRIPTION FACTOR NETWORKS
被引:4
作者:
Luo, Xiangyu
[1
]
Wei, Yingying
[2
]
机构:
[1] Chinese Univ Hong Kong, Dept Stat, G26 Lady Shaw Bldg, Shatin, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Dept Stat, 111 Lady Shaw Bldg, Shatin, Hong Kong, Peoples R China
关键词:
Poisson graphical model;
nonparametric Bayes;
parallel Markov chain Monte Carlo;
next generation sequencing;
INVERSE COVARIANCE ESTIMATION;
SELECTIVE GENE-EXPRESSION;
GAUSSIAN GRAPHICAL MODELS;
NF-KAPPA-B;
VARIABLE SELECTION;
PROTEIN;
DISTRIBUTIONS;
ENCYCLOPEDIA;
FRAMEWORK;
INFERENCE;
D O I:
10.1214/17-AOAS1129
中图分类号:
O21 [概率论与数理统计];
C8 [统计学];
学科分类号:
020208 ;
070103 ;
0714 ;
摘要:
Gene expression is largely controlled by transcription factors (TFs) in a collaborative manner. Therefore, an understanding of TF collaboration is crucial for the elucidation of gene regulation. The co-activation of TFs can be represented by networks. These networks are dynamic in diverse biological conditions and heterogeneous across the genome within each biological condition. Existing methods for construction of TF networks lack solid statistical models, analyze each biological condition separately, and enforce a single network for all genomic locations within one biological condition, resulting in low statistical power and misleading spurious associations. In this paper, we present a novel Bayesian nonparametric dynamic Poisson graphical model for inference on TF networks. Our approach automatically teases out genome heterogeneity and borrows information across conditions to improve signal detection from very few replicates, thus offering a valid and efficient measure of TF co-activations. We develop an efficient parallel Markov chain Monte Carlo algorithm for posterior computation. The proposed approach is applied to study TF associations in ENCODE cell lines and provides novel findings.
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页码:1749 / 1772
页数:24
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