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Controlling false discoveries in high-dimensional situations: boosting with stability selection

Overview of attention for article published in BMC Bioinformatics, May 2015
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Title
Controlling false discoveries in high-dimensional situations: boosting with stability selection
Published in
BMC Bioinformatics, May 2015
DOI 10.1186/s12859-015-0575-3
Pubmed ID
Authors

Benjamin Hofner, Luigi Boccuto, Markus Göker

Abstract

Modern biotechnologies often result in high-dimensional data sets with many more variables than observations (n≪p). These data sets pose new challenges to statistical analysis: Variable selection becomes one of the most important tasks in this setting. Similar challenges arise if in modern data sets from observational studies, e.g., in ecology, where flexible, non-linear models are fitted to high-dimensional data. We assess the recently proposed flexible framework for variable selection called stability selection. By the use of resampling procedures, stability selection adds a finite sample error control to high-dimensional variable selection procedures such as Lasso or boosting. We consider the combination of boosting and stability selection and present results from a detailed simulation study that provide insights into the usefulness of this combination. The interpretation of the used error bounds is elaborated and insights for practical data analysis are given. Stability selection with boosting was able to detect influential predictors in high-dimensional settings while controlling the given error bound in various simulation scenarios. The dependence on various parameters such as the sample size, the number of truly influential variables or tuning parameters of the algorithm was investigated. The results were applied to investigate phenotype measurements in patients with autism spectrum disorders using a log-linear interaction model which was fitted by boosting. Stability selection identified five differentially expressed amino acid pathways. Stability selection is implemented in the freely available R package stabs ( http://CRAN.R-project.org/package=stabs ). It proved to work well in high-dimensional settings with more predictors than observations for both, linear and additive models. The original version of stability selection, which controls the per-family error rate, is quite conservative, though, this is much less the case for its improvement, complementary pairs stability selection. Nevertheless, care should be taken to appropriately specify the error bound.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 102 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Netherlands 1 <1%
United States 1 <1%
China 1 <1%
Unknown 99 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 27 26%
Researcher 20 20%
Student > Master 16 16%
Other 6 6%
Professor 6 6%
Other 14 14%
Unknown 13 13%
Readers by discipline Count As %
Agricultural and Biological Sciences 16 16%
Computer Science 14 14%
Mathematics 12 12%
Medicine and Dentistry 10 10%
Biochemistry, Genetics and Molecular Biology 8 8%
Other 25 25%
Unknown 17 17%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 22 November 2016.
All research outputs
#15,393,913
of 22,901,818 outputs
Outputs from BMC Bioinformatics
#5,388
of 7,302 outputs
Outputs of similar age
#156,991
of 264,584 outputs
Outputs of similar age from BMC Bioinformatics
#97
of 121 outputs
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