GNLGFeb 1, 2024

A Comparative Analysis of Gene Expression Profiling by Statistical and Machine Learning Approaches

arXiv:2402.00926v14 citationsh-index: 13Bioinform Adv
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This work addresses the reliability of gene selection for biological interpretation in cancer research, highlighting incremental insights into methodological limitations.

The study compared machine learning and statistical methods for ranking genes in cancer classification from expression data, finding that while both can identify biomarkers for good classification, the selected genes differ significantly and similar performance can be achieved with many lower-ranked genes, questioning the completeness of explainability.

Many machine learning models have been proposed to classify phenotypes from gene expression data. In addition to their good performance, these models can potentially provide some understanding of phenotypes by extracting explanations for their decisions. These explanations often take the form of a list of genes ranked in order of importance for the predictions, the highest-ranked genes being interpreted as linked to the phenotype. We discuss the biological and the methodological limitations of such explanations. Experiments are performed on several datasets gathering cancer and healthy tissue samples from the TCGA, GTEx and TARGET databases. A collection of machine learning models including logistic regression, multilayer perceptron, and graph neural network are trained to classify samples according to their cancer type. Gene rankings are obtained from explainability methods adapted to these models, and compared to the ones from classical statistical feature selection methods such as mutual information, DESeq2, and EdgeR. Interestingly, on simple tasks, we observe that the information learned by black-box neural networks is related to the notion of differential expression. In all cases, a small set containing the best-ranked genes is sufficient to achieve a good classification. However, these genes differ significantly between the methods and similar classification performance can be achieved with numerous lower ranked genes. In conclusion, although these methods enable the identification of biomarkers characteristic of certain pathologies, our results question the completeness of the selected gene sets and thus of explainability by the identification of the underlying biological processes.

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