Jump to ContentJump to Main Navigation

Statistical Applications in Genetics and Molecular Biology

Editor-in-Chief: Stumpf, Michael P.H.

6 Issues per year

IMPACT FACTOR 2013: 1.055
Rank 48 out of 119 in category Statistics & Probability in the 2013 Thomson Reuters Journal Citation Report/Science Edition

SCImago Journal Rank (SJR): 0.875
Source Normalized Impact per Paper (SNIP): 0.540


Extensions of Sparse Canonical Correlation Analysis with Applications to Genomic Data

Daniela M Witten1 / Robert J. Tibshirani2

1Stanford University

2Stanford University

Citation Information: Statistical Applications in Genetics and Molecular Biology. Volume 8, Issue 1, Pages 1–27, ISSN (Online) 1544-6115, DOI: 10.2202/1544-6115.1470, June 2009

Publication History

Published Online:

In recent work, several authors have introduced methods for sparse canonical correlation analysis (sparse CCA). Suppose that two sets of measurements are available on the same set of observations. Sparse CCA is a method for identifying sparse linear combinations of the two sets of variables that are highly correlated with each other. It has been shown to be useful in the analysis of high-dimensional genomic data, when two sets of assays are available on the same set of samples. In this paper, we propose two extensions to the sparse CCA methodology. (1) Sparse CCA is an unsupervised method; that is, it does not make use of outcome measurements that may be available for each observation (e.g., survival time or cancer subtype). We propose an extension to sparse CCA, which we call sparse supervised CCA, which results in the identification of linear combinations of the two sets of variables that are correlated with each other and associated with the outcome. (2) It is becoming increasingly common for researchers to collect data on more than two assays on the same set of samples; for instance, SNP, gene expression, and DNA copy number measurements may all be available. We develop sparse multiple CCA in order to extend the sparse CCA methodology to the case of more than two data sets. We demonstrate these new methods on simulated data and on a recently published and publicly available diffuse large B-cell lymphoma data set.

Keywords: sparse canonical correlation analysis; gene expression; microarray; DNA copy number; CGH; SNP; lasso; fused lasso

Comments (0)

Please log in or register to comment.
Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.