Imperial College London

DrSethFlaxman

Faculty of Natural SciencesDepartment of Mathematics

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s.flaxman

 
 
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Location

 

522Huxley BuildingSouth Kensington Campus

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Summary

 

Publications

Citation

BibTex format

@article{Crawford:2019:10.1214/18-AOAS1222,
author = {Crawford, L and Flaxman, SR and Runcie, DE and West, M},
doi = {10.1214/18-AOAS1222},
journal = {Annals of Applied Statistics},
pages = {958--989},
title = {Variable prioritization in nonlinear black box methods: a genetic association case study},
url = {http://dx.doi.org/10.1214/18-AOAS1222},
volume = {13},
year = {2019}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - The central aim in this paper is to address variable selection questions in nonlinear and nonparametric regression. Motivated by statistical genetics, where nonlinear interactions are of particular interest, we introduce a novel and interpretable way to summarize the relative importance of predictor variables. Methodologically, we develop the “RelATive cEntrality” (RATE) measure to prioritize candidate genetic variants that are not just marginally important, but whose associations also stem from significant covarying relationships with other variants in the data. We illustrate RATE through Bayesian Gaussian process regression, but the methodological innovations apply to other “black box” methods. It is known that nonlinear models often exhibit greater predictive accuracy than linear models, particularly for phenotypes generated by complex genetic architectures. With detailed simulations and two real data association mapping studies, we show that applying RATE enables an explanation for this improved performance.
AU - Crawford,L
AU - Flaxman,SR
AU - Runcie,DE
AU - West,M
DO - 10.1214/18-AOAS1222
EP - 989
PY - 2019///
SN - 1932-6157
SP - 958
TI - Variable prioritization in nonlinear black box methods: a genetic association case study
T2 - Annals of Applied Statistics
UR - http://dx.doi.org/10.1214/18-AOAS1222
UR - http://arxiv.org/abs/1801.07318v3
UR - http://hdl.handle.net/10044/1/65564
VL - 13
ER -