Evidence map›Paper›PMID 38837347›Full record

ArticleBioinformatics (Oxford, England)2024

Improving the performance and interpretability on medical datasets using graphical ensemble feature selection.

Enzo Battistella, Dina Ghiassian, Albert-László Barabási

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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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

3 authors.

Enzo BattistellaNetwork Science Institute, Northeastern University, Boston, MA 02115, United States.ORCID 0000-0001-7053-5666
Dina GhiassianScipher Medicine, Waltham, MA 02453, United States.
Albert-László BarabásiNetwork Science Institute, Northeastern University, Boston, MA 02115, United States.

Funding

United States Department of Veteran Affairs and Scipher Medicine
6 · The paper itself

Abstract

motivationA major hindrance towards using Machine Learning (ML) on medical datasets is the discrepancy between a large number of variables and small sample sizes. While multiple feature selection techniques have been proposed to avoid the resulting overfitting, overall ensemble techniques offer the best selection robustness. Yet, current methods designed to combine different algorithms generally fail to leverage the dependencies identified by their components. Here, we propose Graphical Ensembling (GE), a graph-theory-based ensemble feature selection technique designed to improve the stability and relevance of the selected features.

resultsRelying on four datasets, we show that GE increases classification performance with fewer selected features. For example, on rheumatoid arthritis patient stratification, GE outperforms the baseline methods by 9% Balanced Accuracy while relying on fewer features. We use data on sub-cellular networks to show that the selected features (proteins) are closer to the known disease genes, and the uncovered biological mechanisms are more diversified. By successfully tackling the complex correlations between biological variables, we anticipate that GE will improve the medical applications of ML. AVAILABILITY AND IMPLEMENTATION: https://github.com/ebattistella/auto_machine_learning.

Indexed as

AlgorithmsMachine LearningArthritis, RheumatoidComputational BiologyHumans

Identifiers

PMID38837347
PMCPMC11187494

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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.