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Brent W. Zanke

Publications and source records attributed to Brent W. Zanke.

2 recordsLinked to original sources

Principal component of explained variance: an efficient and optimal data dimension reduction framework for association studies

The genomics era has led to an increase in the dimensionality of the data collected to investigate biological questions. In this context, dimension-reduction techniques can be used to summarize high-dimensional signals into low-dimensional ones, to further test for association with one or more covariates of interest. This paper revisits one such approach, previously known as Principal Component of Heritability and renamed here as Principal Component of Explained Variance (PCEV). As its name suggests, the PCEV seeks a linear combination of outcomes in an optimal manner, by maximising the proportion of variance explained by one or several covariates of interest. By construction, this method optimises power but limited by its computational complexity, it has unfortunately received little attention in the past. Here, we propose a general analytical PCEV framework that builds on the assets of the original method, i.e. conceptually simple and free of tuning parameters. Moreover, our framework extends the range of applications of the original procedure by providing a computationally simple strategy for high-dimensional outcomes, along with exact and asymptotic testing procedures that drastically reduce its computational cost. We investigate the merits of the PCEV using an extensive set of simulations. Furthermore, the use of the PCEV approach will be illustrated using three examples taken from the epigenetics and brain imaging areas.

Bioinformatics

Functional normalization of 450k methylation array data improves replication in large cancer studies

We propose an extension to quantile normalization which removes unwanted technical variation using control probes. We adapt our algorithm, functional normalization, to the Illumina 450k methylation array and address the open problem of normalizing methylation data with global epigenetic changes, such as human cancers. Using datasets from The Cancer Genome Atlas and a large case-control study, we show that our algorithm outperforms all existing normalization methods with respect to replication of results between experiments, and yields robust results even in the presence of batch effects. Functional normalization can be applied to any microarray platform, provided suitable control probes are available.

Bioinformatics