Skip to content
AI News HubLIVE
Source content · Analysis pending2 min read

Do Vision CIL Methods Transfer to Protein? A Diagnostic Benchmark of Frozen Protein Encoders

Summary

arXiv:2610.18879v1 Announce Type: new Abstract: Protein function annotation operates over an expanding label space, making class-incremental learning (CIL) a natural framework for incorporating newly discovered functions without full retraining. Yet existing CIL methods have been developed largely in vision and have not been systematically evaluated over frozen protein representations. We conduct a controlled benchmark of nine representative CIL methods across five sequence-, structure-, and sequence--structure-based protein encoders and two enzyme function datasets at different scales, while keeping the encoders frozen and evaluation settings consistent across representations. We find that no method transfers reliably across encoders, and that these failures persist across alternative ph…

SourcearXiv Machine LearningAuthor: Ziyuan Gao
Do Vision CIL Methods Transfer to Protein? A Diagnostic Benchmark of Frozen Protein Encoders
Report an error

The correction channel is not available yet. You can copy the article reference below for later.

Correction instructions
Read article

[Submitted on 1 Oct 2026]

Title:Do Vision CIL Methods Transfer to Protein? A Diagnostic Benchmark of Frozen Protein Encoders

View a PDF of the paper titled Do Vision CIL Methods Transfer to Protein? A Diagnostic Benchmark of Frozen Protein Encoders, by Ziyuan Gao

View PDF HTML (experimental)

Abstract:Protein function annotation operates over an expanding label space, making class-incremental learning (CIL) a natural framework for incorporating newly discovered functions without full retraining. Yet existing CIL methods have been developed largely in vision and have not been systematically evaluated over frozen protein representations. We conduct a controlled benchmark of nine representative CIL methods across five sequence-, structure-, and sequence--structure-based protein encoders and two enzyme function datasets at different scales, while keeping the encoders frozen and evaluation settings consistent across representations. We find that no method transfers reliably across encoders, and that these failures persist across alternative phase constructions. Diagnostic analyses reveal that this instability arises from weak gradient-based stability signals, substantial heterogeneity in embedding geometry, and covariance assumptions whose appropriate capacity changes with both dataset scale and encoder. These findings suggest that the representation itself should be treated as a central component of continual-learning design rather than a passive feature extractor. More generally, reliable protein CIL will require encoder-aware methods that adapt their statistical assumptions and capacity to the geometry of the representation on which they operate. Code is available at this https URL.

Comments: Accepted at NeurIPS 2026 Workshop on Continual Learning for Foundation Models and Agents (CL4FM Agents)

Subjects:

Machine Learning (cs.LG); Artificial Intelligence (cs.AI); Quantitative Methods (q-bio.QM)

Cite as: arXiv:2610.18879 [cs.LG]

(or arXiv:2610.18879v1 [cs.LG] for this version)

https://doi.org/10.48550/arXiv.2610.18879

arXiv-issued DOI via DataCite

Submission history

From: Ziyuan Gao [view email] [v1] Thu, 1 Oct 2026 02:12:27 UTC (4,971 KB)

Full-text links:

Access Paper:

View a PDF of the paper titled Do Vision CIL Methods Transfer to Protein? A Diagnostic Benchmark of Frozen Protein Encoders, by Ziyuan Gao

View PDF

HTML (experimental)

TeX Source

view license

Additional Features

Audio Summary

Current browse context:

cs.LG

new | recent | 2026-10

Change to browse by:

cs cs.AI q-bio q-bio.QM

References & Citations

NASA ADS

Google Scholar

Semantic Scholar

Loading...

Data provided by:

Bibliographic Tools

Bibliographic and Citation Tools

Bibliographic Explorer Toggle

Bibliographic Explorer (What is the Explorer?)

Connected Papers Toggle

Connected Papers (What is Connected Papers?)

Litmaps Toggle

Litmaps (What is Litmaps?)

scite.ai Toggle

scite Smart Citations (What are Smart Citations?)

Code, Data, Media

Code, Data and Media Associated with this Article

alphaXiv Toggle

alphaXiv (What is alphaXiv?)

Links to Code Toggle

CatalyzeX Code Finder for Papers (What is CatalyzeX?)

DagsHub Toggle

DagsHub (What is DagsHub?)

GotitPub Toggle

Gotit.pub (What is GotitPub?)

Huggingface Toggle

Hugging Face (What is Huggingface?)

ScienceCast Toggle

ScienceCast (What is ScienceCast?)

Demos

Demos

Replicate Toggle

Replicate (What is Replicate?)

Spaces Toggle

Hugging Face Spaces (What is Spaces?)

Spaces Toggle

TXYZ.AI (What is TXYZ.AI?)

Related Papers

Recommenders and Search Tools

Link to Influence Flower

Influence Flower (What are Influence Flowers?)

Core recommender toggle

CORE Recommender (What is CORE?)

IArxiv recommender toggle

IArxiv Recommender (What is IArxiv?)

Author

Venue

Institution

Topic

About arXivLabs

arXivLabs: experimental projects with community collaborators

arXivLabs is a framework that allows collaborators to develop and share new arXiv features directly on our website.

Both individuals and organizations that work with arXivLabs have embraced and accepted our values of openness, community, excellence, and user data privacy. arXiv is committed to these values and only works with partners that adhere to them.

Have an idea for a project that will add value for arXiv's community? Learn more about arXivLabs.

Which authors of this paper are endorsers? | Disable MathJax (What is MathJax?)

Key points and analysis

Article intelligence

InvestorsAdvanced

Key points

  • AI generation is temporarily unavailable; this entry was preserved with deterministic fallback metadata.
  • arXiv:2610.18879v1 Announce Type: new Abstract: Protein function annotation operates over an expanding label space, making class-incremental learning (CIL) a natural framework for…

Highlights and analysis are generated automatically and may contain errors. Check the original source.