Long-range gene expression prediction with token alignment of large language model

Fuente: arXiv
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Autori principali: Honig, Edouardo, Zhan, Huixin, Wu, Ying Nian, Zhang, Zijun Frank
Natura: Preprint
Pubblicazione: 2024
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author Honig, Edouardo
Zhan, Huixin
Wu, Ying Nian
Zhang, Zijun Frank
author_facet Honig, Edouardo
Zhan, Huixin
Wu, Ying Nian
Zhang, Zijun Frank
contents Gene expression is a cellular process that plays a fundamental role in human phenotypical variations and diseases. Despite advances of deep learning models for gene expression prediction, recent benchmarks have revealed their inability to learn distal regulatory grammar. Here, we address this challenge by leveraging a pretrained large language model to enhance gene expression prediction. We introduce Genetic sequence Token Alignment (GTA), which aligns genetic sequence features with natural language tokens, allowing for symbolic reasoning of genomic sequence features via the frozen language model. This cross-modal adaptation learns the regulatory grammar and allows us to further incorporate gene-specific human annotations as prompts, enabling in-context learning that is not possible with existing models. Trained on lymphoblastoid cells, GTA was evaluated on cells from the Geuvadis consortium and outperforms state-of-the-art models such as Enformer, achieving a Spearman correlation of 0.65, a 10\% improvement. Additionally, GTA offers improved interpretation of long-range interactions through the identification of the most meaningful sections of the input genetic context. GTA represents a powerful and novel cross-modal approach to gene expression prediction by utilizing a pretrained language model, in a paradigm shift from conventional gene expression models trained only on sequence data.
format Preprint
id arxiv_https___arxiv_org_abs_2410_01858
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Long-range gene expression prediction with token alignment of large language model
Honig, Edouardo
Zhan, Huixin
Wu, Ying Nian
Zhang, Zijun Frank
Cell Behavior
Machine Learning
Genomics
Gene expression is a cellular process that plays a fundamental role in human phenotypical variations and diseases. Despite advances of deep learning models for gene expression prediction, recent benchmarks have revealed their inability to learn distal regulatory grammar. Here, we address this challenge by leveraging a pretrained large language model to enhance gene expression prediction. We introduce Genetic sequence Token Alignment (GTA), which aligns genetic sequence features with natural language tokens, allowing for symbolic reasoning of genomic sequence features via the frozen language model. This cross-modal adaptation learns the regulatory grammar and allows us to further incorporate gene-specific human annotations as prompts, enabling in-context learning that is not possible with existing models. Trained on lymphoblastoid cells, GTA was evaluated on cells from the Geuvadis consortium and outperforms state-of-the-art models such as Enformer, achieving a Spearman correlation of 0.65, a 10\% improvement. Additionally, GTA offers improved interpretation of long-range interactions through the identification of the most meaningful sections of the input genetic context. GTA represents a powerful and novel cross-modal approach to gene expression prediction by utilizing a pretrained language model, in a paradigm shift from conventional gene expression models trained only on sequence data.
title Long-range gene expression prediction with token alignment of large language model
topic Cell Behavior
Machine Learning
Genomics
url https://arxiv.org/abs/2410.01858