Abstract

NCBI has been accumulating a large repository of microarray data sets, namely Gene Expression Omnibus (GEO). GEO is a great resource enabling one to pursue various biological and pathological questions. The question we ask here is: given a set of gene signatures and a classifier, what is the best minimum sample size in a clinical microarray research that can effectively distinguish different types of patient responses to a therapeutic drug. It is difficult to answer the question since the sample size for most microarray experiments stored in GEO is very limited. This paper presents a Monte Carlo approach to simulating the best minimum microarray sample size based on the available data sets. Support Vector Machine (SVM) is used as a classifier to compute prediction accuracy for different sample size. Then, a logistic function is applied to fit the relationship between sample size and accuracy whereby a theoretic minimum sample size can be derived.

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