Bipartite graph partitioning and data clustering
Proceedings of the tenth international conference on Information and knowledge management
Information-theoretic co-clustering
Proceedings of the ninth ACM SIGKDD international conference on Knowledge discovery and data mining
Feature selection, L1 vs. L2 regularization, and rotational invariance
ICML '04 Proceedings of the twenty-first international conference on Machine learning
Pattern Recognition and Machine Learning (Information Science and Statistics)
Pattern Recognition and Machine Learning (Information Science and Statistics)
Permutation, Parametric, and Bootstrap Tests of Hypotheses (Springer Series in Statistics)
Permutation, Parametric, and Bootstrap Tests of Hypotheses (Springer Series in Statistics)
Scalable training of L1-regularized log-linear models
Proceedings of the 24th international conference on Machine learning
Weighted Graph Cuts without Eigenvectors A Multilevel Approach
IEEE Transactions on Pattern Analysis and Machine Intelligence
Bioinformatics
Graph theoretical approach to study eQTL
Bioinformatics
Accounting for non-genetic factors improves the power of eQTL studies
RECOMB'08 Proceedings of the 12th annual international conference on Research in computational molecular biology
Flexible and robust co-regularized multi-domain graph clustering
Proceedings of the 19th ACM SIGKDD international conference on Knowledge discovery and data mining
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Genome-wide expression quantitative trait loci (eQTL) studies have emerged as a powerful tool to understand the genetic basis of gene expression and complex traits. The traditional eQTL methods focus on testing the associations between individual single-nucleotide polymorphisms (SNPs) and gene expression traits. A major drawback of this approach is that it cannot model the joint effect of a set of SNPs on a set of genes, which may corresponds to biological pathways. In this paper, we propose a sparse (l1-regularized) graphical model, SET-eQTL, to identify novel associations between sets of SNPs and sets of genes. Such associations are captured by hidden variables connecting SNPs and genes. These hidden variables also naturally model the potential effect of unknown confounding factors. We compare three different methods on a yeast segregant dataset. Extensive experimental results demonstrate that the proposed graphical model SET-eQTL achieves better performance than the other two alternatives.