Abstract

Complex, high-dimensional data sets pose significant analytical challenges in the post-genomic era. Such data sets are not exclusive to genetic analyses and are also pertinent to epidemiology. There has been considerable effort to develop hypothesis-free data mining and machine learning methodologies. However, current methodologies lack exhaustivity and general applicability. Here we use a novel non-parametric, non-euclidean data mining tool, HyperCube®, to explore exhaustively a complex epidemiological malaria data set by searching for over density of events in m-dimensional space. Hotspots of over density correspond to strings of variables, rules, that determine, in this case, the occurrence of Plasmodium falciparum clinical malaria episodes. The data set contained 46,837 outcome events from 1,653 individuals and 34 explanatory variables. The best predictive rule contained 1,689 events from 148 individuals and was defined as: individuals present during 1992–2003, aged 1–5 years old, having hemoglobin AA, and having had previous Plasmodium malariae malaria parasite infection ≤10 times. These individuals had 3.71 times more P. falciparum clinical malaria episodes than the general population. We validated the rule in two different cohorts. We compared and contrasted the HyperCube® rule with the rules using variables identified by both traditional statistical methods and non-parametric regression tree methods. In addition, we tried all possible sub-stratified quantitative variables. No other model with equal or greater representativity gave a higher Relative Risk. Although three of the four variables in the rule were intuitive, the effect of number of P. malariae episodes was not. HyperCube® efficiently sub-stratified quantitative variables to optimize the rule and was able to identify interactions among the variables, tasks not easy to perform using standard data mining methods. Search of local over density in m-dimensional space, explained by easily interpretable rules, is thus seemingly ideal for generating hypotheses for large datasets to unravel the complexity inherent in biological systems.

Highlights

  • Identifying the key variables of a biological system that determine the outcome of interest is difficult

  • The dependant variable was defined as a binary trait: individuals with at least one clinical Plasmodium falciparum malaria attack (PFA) during that trimester or without PFA

  • We describe here a new data mining algorithm that can identify the combinations of variables that give the optimal prediction of the outcome of interest

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Summary

Introduction

Identifying the key variables of a biological system that determine the outcome of interest is difficult. Are there potentially many factors involved, but they do not work independently. Testing for all possible interactions is almost impossible both with respect to statistical validation and biological interpretation. There is a need for data mining tools to explore large and complex biological data sets to identify combinations of factors that optimally explain the outcome of interest. Hypothesisfree data exploration can potentially generate novel hypotheses that emerge from the data and which are beyond our imagination. These novel hypotheses can subsequently be tested using standard statistical methods

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