Evidence map›Paper›PMID 39605589›Full record

ArticlebioRxiv : the preprint server for biology2025

Medium-sized protein language models perform well at transfer learning on realistic datasets.

Luiz C Vieira, Morgan L Handojo, Claus O Wilke

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors.

Luiz C VieiraDepartment of Integrative Biology, The University of Texas at Austin, Austin, TX, United States of America.
Morgan L HandojoDepartment of Integrative Biology, The University of Texas at Austin, Austin, TX, United States of America.
Claus O WilkeDepartment of Integrative Biology, The University of Texas at Austin, Austin, TX, United States of America.ORCID 0000-0002-7470-9261

Funding

Enteroviral 2C protein as a therapeutic targetR01AI169462 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI CRAIG E. CAMERON · 2022 to 2026
$3.8M
The biophysical basis of translational selectionR01GM088344 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI BARRICK, JEFFREY EVAN, WILKE, CLAUS O · 2009 to 2023
$3.5M
Investigating nanobodies to target multidrug resistant bacterial pathogensR01AI148419 · NIAID · UNIVERSITY OF TEXAS AT AUSTIN · PI DAVIES, BRYAN WILLIAM · 2020 to 2023
$2.8M
From microcin sequence to function: linking sequence variation to antimicrobial activityR56AI179799 · NIAID · UNIVERSITY OF TEXAS AT AUSTIN · PI DAVIES, BRYAN WILLIAM · 2024 to 2024
$726k
NIAID NIH HHS R01 AI148419NIAID NIH HHS R01 AI169462NIAID NIH HHS R56 AI179799NIGMS NIH HHS R01 GM088344
6 · The paper itself

Abstract

Protein language models (pLMs) can offer deep insights into evolutionary and structural properties of proteins. While larger models, such as the 15 billion parameter model ESM-2, promise to capture more complex patterns in sequence space, they also present practical challenges due to their high dimensionality and high computational cost. We systematically evaluated the performance of various ESM-style models across multiple biological datasets to assess the impact of model size on transfer learning via feature extraction. Surprisingly, we found that larger models do not necessarily outperform smaller ones, in particular when data is limited. Medium-sized models, such as ESM-2 650M and ESM C 600M, demonstrated consistently good performance, falling only slightly behind their larger counterparts-ESM-2 15B and ESM C 6B-despite being many times smaller. Additionally, we compared various methods of compressing embeddings prior to transfer learning, and we found that mean embeddings consistently outperformed other compression methods. In summary, ESM C 600M with mean embeddings offers an optimal balance between performance and efficiency, making it a practical and scalable choice for transfer learning in realistic biological applications.

Identifiers

PMID39605589
PMCPMC11601519

What OpenQuestion holds

Textmetadata
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.