Evidence map›Paper›PMID 40890427›Full record

ArticleMolecular systems biology2025

Predicting natural variation in the yeast phenotypic landscape with machine learning.

Sakshi Khaiwal, Matteo De Chiara, Benjamin P Barré, Inigo Barrio-Hernandez, Simon Stenberg, Pedro Beltrao, Jonas Warringer, Gianni Liti

Abstract read
In one paragraph

Article in Molecular systems biology, 2025. 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

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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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.

Sakshi KhaiwalCNRS, INSERM, IRCAN, Côte d'Azur University, Nice, France. sakshi.KHAIWAL@univ-cotedazur.fr.
Matteo De ChiaraCNRS, INSERM, IRCAN, Côte d'Azur University, Nice, France.
Benjamin P BarréCNRS, INSERM, IRCAN, Côte d'Azur University, Nice, France.
Inigo Barrio-HernandezInstitute of Molecular Systems Biology, ETH Zürich, Zürich, 8093, Switzerland.ORCID http://orcid.org/0000-0002-5686-0451
Simon StenbergDepartment of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg, 40530, Sweden.
Pedro BeltraoInstitute of Molecular Systems Biology, ETH Zürich, Zürich, 8093, Switzerland.ORCID http://orcid.org/0000-0002-2724-7703
Jonas WarringerDepartment of Chemistry and Molecular Biology, University of Gothenburg, Gothenburg, 40530, Sweden.ORCID http://orcid.org/0000-0001-6144-2740
Gianni LitiCNRS, INSERM, IRCAN, Côte d'Azur University, Nice, France. gianni.liti@cnrs.fr.ORCID http://orcid.org/0000-0002-2318-0775

Funding

Agence Nationale de la Recherche (ANR) ANR-11-LABX-0028-01Agence Nationale de la Recherche (ANR) ANR-15-IDEX-01Agence Nationale de la Recherche (ANR) ANR-18-CE12-0004Agence Nationale de la Recherche (ANR) ANR-20-CE12-0020Agence Nationale de la Recherche (ANR) ANR-22-CE12-0015Agence Nationale de la Recherche (ANR) ANR-24-CE12-7740EC | Horizon 2020 Framework Programme (H2020) 847581Fondation Bettencourt Schueller (Bettencourt Schueller Foundation) ImpulscienceFondation pour la Recherche Médicale (FRM) EQU202003010413
6 · The paper itself

Abstract

Most organismal traits result from the complex interplay of many genetic and environmental factors, making their prediction difficult. Here, we used machine learning (ML) models to explore phenotype predictions for 223 traits measured across 1011 genome-sequenced Saccharomyces cerevisiae strains isolated worldwide. We benchmarked a ML pipeline with multiple linear and non-linear models to predict phenotypes from genotypes and gene expression, and determined gradient boosting machines as the best-performing model. Gene function disruption scores and gene presence/absence emerged as best predictors, suggesting a considerable contribution of the accessory genome in controlling phenotypes. The prediction accuracy broadly varied among phenotypes, with stress resistance being easier to predict compared to growth across nutrients. ML identified relevant genomic features linked to phenotypes, including high-impact variants with established relationships to phenotypes, despite these being rare in the population. Near-perfect accuracies were achieved when other phenomics data mostly in similar conditions were used, suggesting that useful information can be conveyed across phenotypes. Overall, our study underscores the power of ML to interpret the functional outcome of genetic variants.

Indexed as

Genetic VariationMachine LearningPhenomicsSaccharomyces cerevisiaeBoosting Machine Learning AlgorithmsGene Expression Regulation, FungalGenome, FungalGenotypePhenotypeGenetic VariantsMachine LearningPhenotypesPredictionS. cerevisiae

Identifiers

PMID40890427
PMCPMC12583546

What OpenQuestion holds

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Registered trials

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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.