CrossAttOmics: Multi-Omics data integration with CrossAttention.

Aurélien Beaude, Franck Augé, Farida Zehraoui, Blaise Hanczar
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Abstract

Motivation: Advances in high throughput technologies enabled large access to various types of omics. Each omics provides a partial view of the underlying biological process. Integrating multiple omics layers would help have a more accurate diagnosis. However, the complexity of omics data requires approaches that can capture complex relationships. One way to accomplish this is by exploiting the known regulatory links between the different omics, which could help in constructing a better multimodal representation.

Results: In this article, we propose CrossAttOmics, a new deep-learning architecture based on the cross-attention mechanism for multi-omics integration. Each modality is projected in a lower dimensional space with its specific encoder. Interactions between modalities with known regulatory links are computed in the feature representation space with cross-attention. The results of different experiments carried out in this paper show that our model can accurately predict the types of cancer by exploiting the interactions between multiple modalities. CrossAttOmics outperforms other methods when there are few paired training examples. Our approach can be combined with attribution methods like LRP to identify which interactions are the most important.

Availability: The code is available at https://github.com/Sanofi-Public/CrossAttOmics and https://doi.org/10.5281/zenodo.15065928. TCGA data can be downloaded from the Genomic Data Commons Data Portal. CCLE data can be downloaded from the depmap portal.

Supplementary information: Supplementary data are available at Bioinformatics online.

crosssattomics:多组学数据集成与交叉注意。
动机:高通量技术的进步使各种类型的组学得以大量使用。每个组学都提供了潜在生物过程的部分视图。整合多个组学层将有助于更准确的诊断。然而,组学数据的复杂性需要能够捕捉复杂关系的方法。实现这一目标的一种方法是利用不同组学之间已知的调控联系,这有助于构建更好的多模态表示。结果:在本文中,我们提出了一种新的基于交叉注意机制的深度学习架构,用于多组学集成。每种模态都用其特定的编码器在较低维空间中进行投影。具有已知调节链接的模态之间的相互作用在具有交叉注意的特征表示空间中计算。本文进行的不同实验结果表明,我们的模型可以利用多种模式之间的相互作用来准确预测癌症的类型。当配对训练样本很少时,crosssattomics优于其他方法。我们的方法可以与LRP等归因方法相结合,以确定哪些交互是最重要的。可用性:该代码可在https://github.com/Sanofi-Public/CrossAttOmics和https://doi.org/10.5281/zenodo.15065928上获得。TCGA数据可以从基因组数据共享数据门户下载。可以从depmap门户下载CCLE数据。补充信息:补充数据可在生物信息学在线获取。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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