4,706 research outputs found
A Cluster Elastic Net for Multivariate Regression
We propose a method for estimating coefficients in multivariate regression
when there is a clustering structure to the response variables. The proposed
method includes a fusion penalty, to shrink the difference in fitted values
from responses in the same cluster, and an L1 penalty for simultaneous variable
selection and estimation. The method can be used when the grouping structure of
the response variables is known or unknown. When the clustering structure is
unknown the method will simultaneously estimate the clusters of the response
and the regression coefficients. Theoretical results are presented for the
penalized least squares case, including asymptotic results allowing for p >> n.
We extend our method to the setting where the responses are binomial variables.
We propose a coordinate descent algorithm for both the normal and binomial
likelihood, which can easily be extended to other generalized linear model
(GLM) settings. Simulations and data examples from business operations and
genomics are presented to show the merits of both the least squares and
binomial methods.Comment: 37 Pages, 11 Figure
Combining Quadratic Penalization and Variable Selection via Forward Boosting
Quadratic penalties can be used to incorporate external knowledge about the association structure among regressors. Unfortunately, they do not enforce single estimated regression coefficients to equal zero. In this paper we propose a new approach to combine quadratic penalization and variable selection within the framework of generalized linear models. The new method is called Forward Boosting and is related to componentwise boosting techniques. We demonstrate in simulation studies and a real-world data example that the new approach competes well with existing alternatives especially when the focus is on interpretable structuring of predictors
Sparse integrative clustering of multiple omics data sets
High resolution microarrays and second-generation sequencing platforms are
powerful tools to investigate genome-wide alterations in DNA copy number,
methylation and gene expression associated with a disease. An integrated
genomic profiling approach measures multiple omics data types simultaneously in
the same set of biological samples. Such approach renders an integrated data
resolution that would not be available with any single data type. In this
study, we use penalized latent variable regression methods for joint modeling
of multiple omics data types to identify common latent variables that can be
used to cluster patient samples into biologically and clinically relevant
disease subtypes. We consider lasso [J. Roy. Statist. Soc. Ser. B 58 (1996)
267-288], elastic net [J. R. Stat. Soc. Ser. B Stat. Methodol. 67 (2005)
301-320] and fused lasso [J. R. Stat. Soc. Ser. B Stat. Methodol. 67 (2005)
91-108] methods to induce sparsity in the coefficient vectors, revealing
important genomic features that have significant contributions to the latent
variables. An iterative ridge regression is used to compute the sparse
coefficient vectors. In model selection, a uniform design [Monographs on
Statistics and Applied Probability (1994) Chapman & Hall] is used to seek
"experimental" points that scattered uniformly across the search domain for
efficient sampling of tuning parameter combinations. We compared our method to
sparse singular value decomposition (SVD) and penalized Gaussian mixture model
(GMM) using both real and simulated data sets. The proposed method is applied
to integrate genomic, epigenomic and transcriptomic data for subtype analysis
in breast and lung cancer data sets.Comment: Published in at http://dx.doi.org/10.1214/12-AOAS578 the Annals of
Applied Statistics (http://www.imstat.org/aoas/) by the Institute of
Mathematical Statistics (http://www.imstat.org
Pathway-Based Genomics Prediction using Generalized Elastic Net.
We present a novel regularization scheme called The Generalized Elastic Net (GELnet) that incorporates gene pathway information into feature selection. The proposed formulation is applicable to a wide variety of problems in which the interpretation of predictive features using known molecular interactions is desired. The method naturally steers solutions toward sets of mechanistically interlinked genes. Using experiments on synthetic data, we demonstrate that pathway-guided results maintain, and often improve, the accuracy of predictors even in cases where the full gene network is unknown. We apply the method to predict the drug response of breast cancer cell lines. GELnet is able to reveal genetic determinants of sensitivity and resistance for several compounds. In particular, for an EGFR/HER2 inhibitor, it finds a possible trans-differentiation resistance mechanism missed by the corresponding pathway agnostic approach
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