Evidence map›Paper›PMID 42324601›Full record

ArticleBioinformatics (Oxford, England)2026

Fitness translocation: improving variant effect prediction with biologically-grounded data augmentation.

Adrien Mialland, Shuzo Fukunaga, Riku Katsuki, Yunfei Dong, Hideki Yamaguchi, Yutaka Saito

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Adrien MiallandArtificial Intelligence Research Center, National Institute of Advanced Industrial Science and Technology (AIST), Tokyo, Japan.ORCID 0000-0001-5359-674X
Shuzo FukunagaUniversity of Toronto, Tronto, Canada.
Riku KatsukiThe University of Electro-Communications, Tokyo, Japan.
Yunfei DongThe University of Tokyo, Chiba, Japan.
Hideki YamaguchiThe University of Tokyo, Chiba, Japan.
Yutaka SaitoArtificial Intelligence Research Center, National Institute of Advanced Industrial Science and Technology (AIST), Tokyo, Japan.ORCID 0000-0002-4853-0153

Funding

Japan Agency for Medical Esearch and Development (AMED) JP19ak0101122Japan Association for Chemical Innovation (JACI) Prize for Encouraging Young ResearcherJapan Society for the Promotion of Science (JSPS) KAKENHI 22H03691New Energy and Industrial Technology Development Organization (NEDO) JPNP14004Osaka University through the HPCI System hp230057Osaka University through the HPCI System hp240075ROIS National Institute of GeneticsSQUID supercomputer at Cybermedia Center
6 · The paper itself

Abstract

motivationData scarcity limits the characterization of protein fitness landscapes and the development of accurate variant effect prediction models. To address this challenge, we introduce fitness translocation, a data augmentation strategy that generates synthetic variants for a target protein by leveraging variant fitness data previously measured in homologous proteins. Using embeddings from protein language models, the method computes the difference between each homolog variant and its wild type and applies these offsets to the target wild-type embedding to create synthetic variants in embedding space.

resultsWe illustrate the utility of fitness translocation in the context of variant effect prediction on three protein families: IGPS, GFP, and SARS-CoV-2 spike proteins, across different models and training data sizes. Fitness translocation consistently improves predictive performance, particularly under limited training data, and is effective even when augmenting with remote homologs sharing as little as 35% sequence identity. These results illustrate how biologically grounded data augmentation can expand and diversify protein fitness landscapes, supporting more data-efficient protein engineering. AVAILABILITY AND IMPLEMENTATION: The code and datasets are available at https://github.com/adrienmialland/ProtFitTrans.

Indexed as

Computational BiologySpike Glycoprotein, CoronavirusGenetic VariationGreen Fluorescent ProteinsHumansPrediction AlgorithmsProtein EngineeringSARS-CoV-2Green Fluorescent ProteinsSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2

Identifiers

PMID42324601
PMCPMC13360282

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LicenceCC BY
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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.