Evidence map›Paper›PMID 36833178›Full record

ArticleGenes2023

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

Álvaro Torres-Martos, Mireia Bustos-Aibar, Alberto Ramírez-Mena, Sofía Cámara-Sánchez, Augusto Anguita-Ruiz, Rafael Alcalá, Concepción M Aguilera, Jesús Alcalá-Fdez

Open access · goldAbstract read
In one paragraph

Article in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.5field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 29 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Álvaro Torres-MartosDepartment of Biochemistry and Molecular Biology II, University of Granada, 18071 Granada, Spain.ORCID 0000-0003-3198-2556
Mireia Bustos-AibarDepartment of Biochemistry and Molecular Biology II, University of Granada, 18071 Granada, Spain.ORCID 0000-0002-2520-8006
Alberto Ramírez-MenaCentre for Genomics and Oncological Research (GENYO), 18016 Granada, Spain.ORCID 0000-0001-9017-8643
Sofía Cámara-SánchezDepartment of Computer Science and Artificial Intelligence, Andalusian Research Institute in Data Science and Computational Intelligence (DaSCI), University of Granada, 18071 Granada, Spain.
Augusto Anguita-Ruiz"José Mataix Verdú" Institute of Nutrition and Food Technology (INYTA), Center of Biomedical Research, University of Granada, 18100 Granada, Spain.ORCID 0000-0001-6888-1041
Rafael AlcaláDepartment of Computer Science and Artificial Intelligence, Andalusian Research Institute in Data Science and Computational Intelligence (DaSCI), University of Granada, 18071 Granada, Spain.ORCID 0000-0003-1140-6156
Concepción M AguileraDepartment of Biochemistry and Molecular Biology II, University of Granada, 18071 Granada, Spain.ORCID 0000-0002-1451-4788
Jesús Alcalá-FdezDepartment of Computer Science and Artificial Intelligence, Andalusian Research Institute in Data Science and Computational Intelligence (DaSCI), University of Granada, 18071 Granada, Spain.ORCID 0000-0002-6190-3575
Universidad de Granada · ESPfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Pediatric ObesityAlgorithmsChildHumansMachine Learningdata pre-processingmachine learningomics

Identifiers

PMID36833178
PMCPMC9956296
OpenAlexW4317426771

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.