利用专家知识进行上位性全基因组分析的合理初始化。

Casey S Greene, Bill C White, Jason H Moore
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引用次数: 14

摘要

在人类遗传学中,现在可以测量人类基因组中大量的DNA序列变化。鉴于目前关于生物网络和疾病过程的知识,疾病风险似乎可以通过生物成分之间的相互作用来最好地建模,这种相互作用可以作为相互作用的DNA序列变化进行检查。机器学习的挑战是有效地探索这些数据集中的相互作用,以识别预测常见人类疾病的变异组合。遗传规划是解决这一问题的一种很有前途的方法。本研究的目的是检验专家知识感知初始化器在遗传规划框架中可以发挥的作用。我们证明了这种专家知识感知的初始化器优于随机初始化器和枚举初始化器。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sensible Initialization Using Expert Knowledge for Genome-Wide Analysis of Epistasis Using Genetic Programming.

In human genetics it is now possible to measure large numbers of DNA sequence variations across the human genome. Given current knowledge about biological networks and disease processes it seems likely that disease risk can best be modeled by interactions between biological components, which may be examined as interacting DNA sequence variations. The machine learning challenge is to effectively explore interactions in these datasets to identify combinations of variations which are predictive of common human diseases. Genetic programming is a promising approach to this problem. The goal of this study is to examine the role that an expert knowledge aware initializer can play in the framework of genetic programming. We show that this expert knowledge aware initializer outperforms both a random initializer and an enumerative initializer.

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