Sari la conținut

Română · beta. Traducerea a fost făcută automat și este încă în curs de revizuire. Citește pagina în engleză

perspectiva aiqbenchMachine learning

analiza aiqbench

This research identifies high sequence entropy as a primary constraint preventing genomic foundation models from achieving the robust capabilities seen in natural language processing. By demonstrating that self-supervised training on DNA alone leads to unstable embeddings and model disagreement, the study challenges the direct transferability of current NLP methodologies to biological data. For practitioners, this implies that architectural or training paradigm adjustments are necessary before expecting foundational model success in genomics.
Sursă care acoperăarXiv

Entropy, Disagreement, and the Limits of Foundation Models in Genomics

arXiv2 min de cititArticolul și perspectiva sunt în engleză.

arXiv:2604.04287v2 Announce Type: replace Abstract: Foundation models in genomics have shown mixed success compared to their counterparts in natural language processing. Yet, the reasons for their limited effectiveness remain poorly understood. In this work, we investigate the role of entropy as a fundamental factor limiting the capacities of such models to learn from their training data and develop foundational capabilities. We train ensembles of models on text and DNA sequences and analyze their predictions, static embeddings, and empirical Fisher information flow. We show that the high entropy of genomic sequences -- from the point of view of unseen token prediction -- leads to near-uniform output distributions, disagreement across models, and unstable static embeddings, even for models that are matched in architecture, training and data. We then demonstrate that models trained on DNA concentrate Fisher information in embedding layers, seemingly failing to exploit inter-token relationships. Our results suggest that self-supervised training from sequences alone may not be applicable to genomic data, calling into question the assumptions underlying current methodologies for training genomic foundation models.

Abstract:Foundation models in genomics have shown mixed success compared to their counterparts in natural language processing. Yet, the reasons for their limited effectiveness remain poorly understood. In this work, we investigate the role of entropy as a fundamental factor limiting the capacities of such models to learn from their training data and develop foundational capabilities. We train ensembles of models on text and DNA sequences and analyze their predictions, static embeddings, and empirical Fisher information flow. We show that the high entropy of genomic sequences -- from the point of view of unseen token prediction -- leads to near-uniform output distributions, disagreement across models, and unstable static embeddings, even for models that are matched in architecture, training and data. We then demonstrate that models trained on DNA concentrate Fisher information in embedding layers, seemingly failing to exploit inter-token relationships. Our results suggest that self-supervised training from sequences alone may not be applicable to genomic data, calling into question the assumptions underlying current methodologies for training genomic foundation models.

Machine Learning (cs.LG); Computation and Language (cs.CL); Genomics (q-bio.GN)

arXiv:2604.04287 [cs.LG]

(or arXiv:2604.04287v2 [cs.LG] for this version)

https://doi.org/10.48550/arXiv.2604.04287 Focus to learn more arXiv-issued DOI via DataCite

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.

Text integral sub licența deschisă a publicației · 266 cuvinte

Subiecte conexe