Omics Data Preprocessing for Machine Learning: A Case Study in Childhood Obesity

Author:

Torres-Martos Álvaro123ORCID,Bustos-Aibar Mireia123ORCID,Ramírez-Mena Alberto4ORCID,Cámara-Sánchez Sofía5,Anguita-Ruiz Augusto2367ORCID,Alcalá Rafael5ORCID,Aguilera Concepción M.1237ORCID,Alcalá-Fdez Jesús5ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology II, University of Granada, 18071 Granada, Spain

2. "José Mataix Verdú" Institute of Nutrition and Food Technology (INYTA), Center of Biomedical Research, University of Granada, 18100 Granada, Spain

3. Biosanitary Research Institute of Granada (IBS.GRANADA), 18012 Granada, Spain

4. Centre for Genomics and Oncological Research (GENYO), 18016 Granada, Spain

5. Department of Computer Science and Artificial Intelligence, Andalusian Research Institute in Data Science and Computational Intelligence (DaSCI), University of Granada, 18071 Granada, Spain

6. Barcelona Institute for Global Health (ISGlobal), 08003 Barcelona, Spain

7. CIBER Physiopathology of Obesity and Nutrition (CIBEROBN), Instituto de Salud Carlos III, 28029 Madrid, Spain

Abstract

The use of machine learning techniques for the construction of predictive models of disease outcomes (based on omics and other types of molecular data) has gained enormous relevance in the last few years in the biomedical field. Nonetheless, the virtuosity of omics studies and machine learning tools are subject to the proper application of algorithms as well as the appropriate pre-processing and management of input omics and molecular data. Currently, many of the available approaches that use machine learning on omics data for predictive purposes make mistakes in several of the following key steps: experimental design, feature selection, data pre-processing, and algorithm selection. For this reason, we propose the current work as a guideline on how to confront the main challenges inherent to multi-omics human data. As such, a series of best practices and recommendations are also presented for each of the steps defined. In particular, the main particularities of each omics data layer, the most suitable preprocessing approaches for each source, and a compilation of best practices and tips for the study of disease development prediction using machine learning are described. Using examples of real data, we show how to address the key problems mentioned in multi-omics research (e.g., biological heterogeneity, technical noise, high dimensionality, presence of missing values, and class imbalance). Finally, we define the proposals for model improvement based on the results found, which serve as the bases for future work.

Funder

ERDF/Regional Government of Andalusia

Ministry of Economic Transformation, Industry, Knowledge, and Universities

ERDF/Health Institute Carlos III

Spanish Ministry of Science, Innovation, and Universities

Publisher

MDPI AG

Subject

Genetics (clinical),Genetics

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