Sequential Monte Carlo multiple testing

被引:27
|
作者
Sandve, Geir Kjetil [1 ]
Ferkingstad, Egil [2 ]
Nygard, Stale [3 ]
机构
[1] Univ Oslo, Dept Informat, N-0316 Oslo, Norway
[2] Norwegian Comp Ctr, Oslo, Norway
[3] Univ Oslo, Oslo Univ Hosp, Inst Med Informat, Bioinformat Core Facil, Oslo, Norway
关键词
TRUE NULL HYPOTHESES; P-VALUES; PROPORTION; NUMBER; METHYLATIONS; MICROARRAY; GENOMICS;
D O I
10.1093/bioinformatics/btr568
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: In molecular biology, as in many other scientific fields, the scale of analyses is ever increasing. Often, complex Monte Carlo simulation is required, sometimes within a large-scale multiple testing setting. The resulting computational costs may be prohibitively high. Results: We here present MCFDR, a simple, novel algorithm for false discovery rate (FDR) modulated sequential Monte Carlo (MC) multiple hypothesis testing. The algorithm iterates between adding MC samples across tests and calculating intermediate FDR values for the collection of tests. MC sampling is stopped either by sequential MC or based on a threshold on FDR. An essential property of the algorithm is that it limits the total number of MC samples whatever the number of true null hypotheses. We show on both real and simulated data that the proposed algorithm provides large gains in computational efficiency.
引用
收藏
页码:3235 / 3241
页数:7
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