摘要:从未配对的单细胞数据中通过循环一致训练进行准确的跨模态翻译。

Siwei Xu, Junhao Liu, Jing Zhang
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引用次数: 0

摘要

单细胞测序技术通过能够同时分析单个细胞内的各种分子模式,彻底改变了基因组学。它们的整合,特别是跨模态翻译,提供了对细胞调控机制的深刻见解。已经开发了许多跨模态翻译方法,但它们对稀缺的高质量联合分析数据的依赖限制了它们的适用性。为了解决这个问题,我们引入了scACT,这是一个深度生成模型,旨在从未配对的单细胞数据中提取跨模态的生物学见解。scACT解决了三个主要挑战:通过对抗性训练对齐未配对的多模态数据,通过循环一致训练在没有先验知识的情况下促进跨模态翻译,以及通过计算机扰动实现可解释的调节互连探索。为了测试其性能,我们将scACT应用于不同的单细胞数据集,发现它在所有三个任务中都优于现有的方法。最后,我们开发了scACT作为一个独立的开源软件包,以促进研究社区内单细胞组学数据的处理和分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
scACT: Accurate Cross-modality Translation via Cycle-consistent Training from Unpaired Single-cell Data.

Single-cell sequencing technologies have revolutionized genomics by enabling the simultaneous profiling of various molecular modalities within individual cells. Their integration, especially cross-modality translation, offers deep insights into cellular regulatory mechanisms. Many methods have been developed for cross-modality translation, but their reliance on scarce high-quality co-assay data limits their applicability. Addressing this, we introduce scACT, a deep generative model designed to extract cross-modality biological insights from unpaired single-cell data. scACT tackles three major challenges: aligning unpaired multi-modal data via adversarial training, facilitating cross-modality translation without prior knowledge via cycle-consistent training, and enabling interpretable regulatory interconnections explorations via in-silico perturbations. To test its performance, we applied scACT on diverse single-cell datasets and found it outperformed existing methods in all three tasks. Finally, we have developed scACT as an individual open-source software package to advance single-cell omics data processing and analysis within the research community.

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