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Priority-Lasso: a simple hierarchical approach to the prediction of clinical outcome using multi-omics data.


ABSTRACT: BACKGROUND:The inclusion of high-dimensional omics data in prediction models has become a well-studied topic in the last decades. Although most of these methods do not account for possibly different types of variables in the set of covariates available in the same dataset, there are many such scenarios where the variables can be structured in blocks of different types, e.g., clinical, transcriptomic, and methylation data. To date, there exist a few computationally intensive approaches that make use of block structures of this kind. RESULTS:In this paper we present priority-Lasso, an intuitive and practical analysis strategy for building prediction models based on Lasso that takes such block structures into account. It requires the definition of a priority order of blocks of data. Lasso models are calculated successively for every block and the fitted values of every step are included as an offset in the fit of the next step. We apply priority-Lasso in different settings on an acute myeloid leukemia (AML) dataset consisting of clinical variables, cytogenetics, gene mutations and expression variables, and compare its performance on an independent validation dataset to the performance of standard Lasso models. CONCLUSION:The results show that priority-Lasso is able to keep pace with Lasso in terms of prediction accuracy. Variables of blocks with higher priorities are favored over variables of blocks with lower priority, which results in easily usable and transportable models for clinical practice.

SUBMITTER: Klau S 

PROVIDER: S-EPMC6134797 | biostudies-literature | 2018 Sep

REPOSITORIES: biostudies-literature

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Priority-Lasso: a simple hierarchical approach to the prediction of clinical outcome using multi-omics data.

Klau Simon S   Jurinovic Vindi V   Hornung Roman R   Herold Tobias T   Boulesteix Anne-Laure AL  

BMC bioinformatics 20180912 1


<h4>Background</h4>The inclusion of high-dimensional omics data in prediction models has become a well-studied topic in the last decades. Although most of these methods do not account for possibly different types of variables in the set of covariates available in the same dataset, there are many such scenarios where the variables can be structured in blocks of different types, e.g., clinical, transcriptomic, and methylation data. To date, there exist a few computationally intensive approaches th  ...[more]

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