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MOSCATO:一种用于分析多组学单细胞数据的有监督方法。

MOSCATO: a supervised approach for analyzing multi-Omic single-Cell data.

机构信息

University at Buffalo, Buffalo, United States.

出版信息

BMC Genomics. 2022 Aug 4;23(1):557. doi: 10.1186/s12864-022-08759-3.

DOI:10.1186/s12864-022-08759-3
PMID:35927608
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9351124/
Abstract

BACKGROUND

Advancements in genomic sequencing continually improve personalized medicine, and recent breakthroughs generate multimodal data on a cellular level. We introduce MOSCATO, a technique for selecting features across multimodal single-cell datasets that relate to clinical outcomes. We summarize the single-cell data using tensors and perform regularized tensor regression to return clinically-associated variable sets for each 'omic' type.

RESULTS

Robustness was assessed over simulations based on available single-cell simulation methods, and applicability was assessed through an example using CITE-seq data to detect genes associated with leukemia. We find that MOSCATO performs favorably in selecting network features while also shown to be applicable to real multimodal single-cell data.

CONCLUSIONS

MOSCATO is a useful analytical technique for supervised feature selection in multimodal single-cell data. The flexibility of our approach enables future extensions on distributional assumptions and covariate adjustments.

摘要

背景

基因组测序技术的进步不断推动着个性化医疗的发展,最近的突破在细胞水平上产生了多模态数据。我们引入了 MOSCATO 技术,用于选择与临床结果相关的多模态单细胞数据集的特征。我们使用张量对单细胞数据进行总结,并执行正则化张量回归,为每种“组学”类型返回与临床相关的变量集。

结果

基于现有的单细胞模拟方法对稳健性进行了评估,并通过使用 CITE-seq 数据检测与白血病相关的基因的示例评估了适用性。我们发现 MOSCATO 在选择网络特征方面表现出色,同时也适用于真实的多模态单细胞数据。

结论

MOSCATO 是一种用于多模态单细胞数据中监督特征选择的有用分析技术。我们方法的灵活性为分布假设和协变量调整的未来扩展提供了可能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/9b9c83a5be68/12864_2022_8759_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/a99ac79c11a8/12864_2022_8759_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/ae445a88d905/12864_2022_8759_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/11828e57020d/12864_2022_8759_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/ef0dfe6489ec/12864_2022_8759_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/edde204787f0/12864_2022_8759_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/17a25f58eb6b/12864_2022_8759_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/9b9c83a5be68/12864_2022_8759_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/a99ac79c11a8/12864_2022_8759_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/ae445a88d905/12864_2022_8759_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/11828e57020d/12864_2022_8759_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/ef0dfe6489ec/12864_2022_8759_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/edde204787f0/12864_2022_8759_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/17a25f58eb6b/12864_2022_8759_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0b2/9351124/9b9c83a5be68/12864_2022_8759_Fig7_HTML.jpg

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