Genomic feature selection by coverage design optimization

Stephen Reid, Aaron M. Newman, Maximilian Diehn, Ash A. Alizadeh and Robert Tibshirani

Journal of Applied Statistics, 2018, vol. 45, issue 14, 2658-2676

Abstract: We introduce a novel data reduction technique whereby we select a subset of tiles to ‘cover’ maximally events of interest in large-scale biological datasets (e.g. genetic mutations), while minimizing the number of tiles. A tile is a genomic unit capturing one or more biological events, such as a sequence of base pairs that can be sequenced and observed simultaneously. The goal is to reduce significantly the number of tiles considered to those with areas of dense events in a cohort, thus saving on cost and enhancing interpretability. However, the reduction should not come at the cost of too much information, allowing for sensible statistical analysis after its application. We envisage application of our methods to a variety of high throughput data types, particularly those produced by next-generation sequencing (NGS) experiments. The procedure is cast as a convex optimization problem, which is presented, along with methods of its solution. The method is demonstrated on a large dataset of somatic mutations spanning 5000+ patients, each having one of 29 cancer types. Applied to these data, our method dramatically reduces the number of gene locations required for broad coverage of patients and their mutations, giving subject specialists a more easily interpretable snapshot of recurrent mutational profiles in these cancers. The locations identified coincide with previously identified cancer genes. Finally, despite considerable data reduction, we show that our covering designs preserve the cancer discrimination ability of multinomial logistic regression models trained on all of the locations ( $ >1M $ >1M).

Date: 2018
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Persistent link: https://EconPapers.repec.org/RePEc:taf:japsta:v:45:y:2018:i:14:p:2658-2676

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DOI: 10.1080/02664763.2018.1432577

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