Quon, Gerald
Diversifying Sparsity Using Variational Determinantal Point Processes
Batmanghelich, Nematollah Kayhan, Quon, Gerald, Kulesza, Alex, Kellis, Manolis, Golland, Polina, Bornn, Luke
We propose a novel diverse feature selection method based on determinantal point processes (DPPs). Our model enables one to flexibly define diversity based on the covariance of features (similar to orthogonal matching pursuit) or alternatively based on side information. We introduce our approach in the context of Bayesian sparse regression, employing a DPP as a variational approximation to the true spike and slab posterior distribution. We subsequently show how this variational DPP approximation generalizes and extends mean-field approximation, and can be learned efficiently by exploiting the fast sampling properties of DPPs. Our motivating application comes from bioinformatics, where we aim to identify a diverse set of genes whose expression profiles predict a tumor type where the diversity is defined with respect to a gene-gene interaction network. We also explore an application in spatial statistics. In both cases, we demonstrate that the proposed method yields significantly more diverse feature sets than classic sparse methods, without compromising accuracy.
A mixture model for the evolution of gene expression in non-homogeneous datasets
Quon, Gerald, Teh, Yee W., Chan, Esther, Hughes, Timothy, Brudno, Michael, Morris, Quaid D.
We address the challenge of assessing conservation of gene expression in complex, non-homogeneous datasets. Recent studies have demonstrated the success of probabilistic models in studying the evolution of gene expression in simple eukaryotic organisms such as yeast, for which measurements are typically scalar and independent. Models capable of studying expression evolution in much more complex organisms such as vertebrates are particularly important given the medical and scientific interest in species such as human and mouse. We present a statistical model that makes a number of significant extensions to previous models to enable characterization of changes in expression among highly complex organisms. We demonstrate the efficacy of our method on a microarray dataset containing diverse tissues from multiple vertebrate species. We anticipate that the model will be invaluable in the study of gene expression patterns in other diverse organisms as well, such as worms and insects.