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翻訳待ち:Do Vision CIL Methods Transfer to Protein? A Diagnostic Benchmark of Frozen Protein Encoders

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AI サービスが一時的に利用できないため、復旧後に翻訳を補完します。ソース概要: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 thes…

ソースarXiv Machine Learning著者: Ziyuan Gao
翻訳待ち:Do Vision CIL Methods Transfer to Protein? A Diagnostic Benchmark of Frozen Protein Encoders
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AI サービスが一時的に利用できないため、復旧後に翻訳を補完します。

[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?)

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  • AI 生成が一時的に利用できないため、ソース内容とフォールバックメタデータを保存しました。
  • 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…

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