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Morbigenous brain region and gene detection with a genetically evolved random neural network cluster approach in late mild cognitive impairment

  • Xia An Bi*
  • , Xia An Bi*
  • , Yingchao Liu
  • , Yingchao Liu
  • , Yiming Xie
  • , Yiming Xie
  • , Xi Hu
  • , Xi Hu
  • , Qinghua Jiang*
  • *Corresponding author for this work
  • Hunan Normal University
  • School of Life Science and Technology, Harbin Institute of Technology

Research output: Contribution to journalArticlepeer-review

Abstract

Motivation: The multimodal data fusion analysis becomes another important field for brain disease detection and increasing researches concentrate on using neural network algorithms to solve a range of problems. However, most current neural network optimizing strategies focus on internal nodes or hidden layer numbers, while ignoring the advantages of external optimization. Additionally, in the multimodal data fusion analysis of brain science, the problems of small sample size and high-dimensional data are often encountered due to the difficulty of data collection and the specialization of brain science data, which may result in the lower generalization performance of neural network. Results: We propose a genetically evolved random neural network cluster (GERNNC) model. Specifically, the fusion characteristics are first constructed to be taken as the input and the best type of neural network is selected as the base classifier to form the initial random neural network cluster. Second, the cluster is adaptively genetically evolved. Based on the GERNNC model, we further construct a multi-Tasking framework for the classification of patients with brain disease and the extraction of significant characteristics. In a study of genetic data and functional magnetic resonance imaging data from the Alzheimer's Disease Neuroimaging Initiative, the framework exhibits great classification performance and strong morbigenous factor detection ability. This work demonstrates that how to effectively detect pathogenic components of the brain disease on the high-dimensional medical data and small samples.

Original languageEnglish
Pages (from-to)2561-2568
Number of pages8
JournalBioinformatics
Volume36
Issue number8
DOIs
StatePublished - 15 Apr 2020
Externally publishedYes

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