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单细胞多模态生成对抗网络揭示三阴性乳腺癌单细胞数据中的空间模式。

Single-cell multi-modal GAN reveals spatial patterns in single-cell data from triple-negative breast cancer.

作者信息

Amodio Matthew, Youlten Scott E, Venkat Aarthi, San Juan Beatriz P, Chaffer Christine L, Krishnaswamy Smita

机构信息

Yale University Department of Computer Science, New Haven, CT, USA.

Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.

出版信息

Patterns (N Y). 2022 Sep 1;3(9):100577. doi: 10.1016/j.patter.2022.100577. eCollection 2022 Sep 9.

DOI:10.1016/j.patter.2022.100577
PMID:36124302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9481959/
Abstract

Exciting advances in technologies to measure biological systems are currently at the forefront of research. The ability to gather data along an increasing number of omic dimensions has created a need for tools to analyze all of this information together, rather than siloing each technology into separate analysis pipelines. To advance this goal, we introduce a framework called the single-cell multi-modal generative adversarial network (scMMGAN) that integrates data from multiple modalities into a unified representation in the ambient data space for downstream analysis using a combination of adversarial learning and data geometry techniques. The framework's key improvement is an additional diffusion geometry loss with a new kernel that constrains the otherwise over-parameterized GAN. We demonstrate scMMGAN's ability to produce more meaningful alignments than alternative methods on a wide variety of data modalities and that its output can be used to draw conclusions from real-world biological experimental data.

摘要

测量生物系统的技术方面令人兴奋的进展目前处于研究前沿。沿着越来越多的组学维度收集数据的能力,使得需要有工具来一起分析所有这些信息,而不是将每种技术孤立地放入单独的分析流程中。为了推进这一目标,我们引入了一个名为单细胞多模态生成对抗网络(scMMGAN)的框架,该框架使用对抗学习和数据几何技术的组合,将来自多个模态的数据整合到环境数据空间中的统一表示中,以便进行下游分析。该框架的关键改进是带有新内核的额外扩散几何损失,它可以约束原本参数过多的生成对抗网络。我们证明,scMMGAN在各种数据模态上比其他方法能够产生更有意义的比对,并且其输出可用于从真实世界的生物学实验数据中得出结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5b/9481959/b32fe8587f58/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5b/9481959/65dde85e9e20/gr1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5b/9481959/b90fc592ea5c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5b/9481959/c2fb0548ae81/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5b/9481959/dafeea2955ce/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5b/9481959/b32fe8587f58/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5b/9481959/65dde85e9e20/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5b/9481959/5956dae8a80f/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5b/9481959/b90fc592ea5c/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5b/9481959/c2fb0548ae81/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5b/9481959/dafeea2955ce/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0c5b/9481959/b32fe8587f58/gr6.jpg

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High SLC2A1 expression associated with suppressing CD8 T cells and B cells promoted cancer survival in gastric cancer.高 SLC2A1 表达与抑制 CD8 T 细胞和 B 细胞有关,促进了胃癌的肿瘤存活。
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