计算机科学
背景(考古学)
深度学习
人工智能
学习迁移
任务(项目管理)
机器学习
下游(制造业)
生物
古生物学
管理
经济
运营管理
作者
Christina V. Theodoris,Ling Xiao,Anant Chopra,Mark Chaffin,Zeina R. Al Sayed,Matthew C. Hill,Helene Mantineo,Elizabeth M. Brydon,Zexian Zeng,X. Shirley Liu,Patrick T. Ellinor
出处
期刊:Nature
[Nature Portfolio]
日期:2023-05-31
卷期号:618 (7965): 616-624
被引量:366
标识
DOI:10.1038/s41586-023-06139-9
摘要
Mapping gene networks requires large amounts of transcriptomic data to learn the connections between genes, which impedes discoveries in settings with limited data, including rare diseases and diseases affecting clinically inaccessible tissues. Recently, transfer learning has revolutionized fields such as natural language understanding1,2 and computer vision3 by leveraging deep learning models pretrained on large-scale general datasets that can then be fine-tuned towards a vast array of downstream tasks with limited task-specific data. Here, we developed a context-aware, attention-based deep learning model, Geneformer, pretrained on a large-scale corpus of about 30 million single-cell transcriptomes to enable context-specific predictions in settings with limited data in network biology. During pretraining, Geneformer gained a fundamental understanding of network dynamics, encoding network hierarchy in the attention weights of the model in a completely self-supervised manner. Fine-tuning towards a diverse panel of downstream tasks relevant to chromatin and network dynamics using limited task-specific data demonstrated that Geneformer consistently boosted predictive accuracy. Applied to disease modelling with limited patient data, Geneformer identified candidate therapeutic targets for cardiomyopathy. Overall, Geneformer represents a pretrained deep learning model from which fine-tuning towards a broad range of downstream applications can be pursued to accelerate discovery of key network regulators and candidate therapeutic targets. A context-aware, attention-based deep learning model pretrained on single-cell transcriptomes enables predictions in settings with limited data in network biology and could accelerate discovery of key network regulators and candidate therapeutic targets.
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