从脑成像表型中学习遗传关联的基础模型。

IF 2.8 Q2 MATHEMATICAL & COMPUTATIONAL BIOLOGY
Bioinformatics advances Pub Date : 2025-08-13 eCollection Date: 2025-01-01 DOI:10.1093/bioadv/vbaf196
Diego Machado Reyes, Myson Burch, Laxmi Parida, Aritra Bose
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引用次数: 0

摘要

动机:由于神经系统疾病的复杂病因学,使用标准方法寻找多组学特征之间可解释的关联可能具有挑战性。结果:我们提出COMICAL,一种使用多组学数据的对比学习方法,以产生遗传标记和脑成像衍生表型之间的关联。COMICAL利用基于转换器的编码器和自定义标记器共同学习组学表示。我们的模态不可知方法通过自监督学习方案和跨模态注意编码器唯一地识别多对多关联。COMICAL在英国生物银行发现了遗传标记和各种神经系统疾病的成像衍生表型之间的几个重要关联,以及从学习表征中预测疾病和看不见的临床结果。可用性和实现:COMICAL的源代码以及预训练的权重,支持迁移学习,可在https://github.com/IBM/comical获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A foundation model for learning genetic associations from brain imaging phenotypes.

A foundation model for learning genetic associations from brain imaging phenotypes.

A foundation model for learning genetic associations from brain imaging phenotypes.

A foundation model for learning genetic associations from brain imaging phenotypes.

Motivation: Due to the intricate etiology of neurological disorders, finding interpretable associations between multiomics features can be challenging using standard approaches.

Results: We propose COMICAL, a contrastive learning approach using multiomics data to generate associations between genetic markers and brain imaging-derived phenotypes. COMICAL jointly learns omics representations utilizing transformer-based encoders with custom tokenizers. Our modality-agnostic approach uniquely identifies many-to-many associations via self-supervised learning schemes and cross-modal attention encoders. COMICAL discovered several significant associations between genetic markers and imaging-derived phenotypes for a variety of neurological disorders in the UK Biobank, as well as prediction of diseases and unseen clinical outcomes from learned representations.

Availability and implementation: The source code of COMICAL along with pretrained weights, enabling transfer learning, is available at https://github.com/IBM/comical.

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