Bi-order multimodal integration of single-cell data

被引:0
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作者
Jinzhuang Dou
Shaoheng Liang
Vakul Mohanty
Qi Miao
Yuefan Huang
Qingnan Liang
Xuesen Cheng
Sangbae Kim
Jongsu Choi
Yumei Li
Li Li
May Daher
Rafet Basar
Katayoun Rezvani
Rui Chen
Ken Chen
机构
[1] The University of Texas MD Anderson Cancer Center,Department of Bioinformatics and Computational Biology
[2] Baylor College of Medicine,Department of Molecular and Human Genetics
[3] The University of Texas MD Anderson Cancer Center,Department of Stem Cell Transplantation and Cellular Therapy
[4] Baylor College of Medicine,Verna and Marrs McLean Department of Biochemistry and Molecular Biology
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Single-cell multi-omics; Bi-order canonical correlation analysis; Cell type identity;
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摘要
Integration of single-cell multiomics profiles generated by different single-cell technologies from the same biological sample is still challenging. Previous approaches based on shared features have only provided approximate solutions. Here, we present a novel mathematical solution named bi-order canonical correlation analysis (bi-CCA), which extends the widely used CCA approach to iteratively align the rows and the columns between data matrices. Bi-CCA is generally applicable to combinations of any two single-cell modalities. Validations using co-assayed ground truth data and application to a CAR-NK study and a fetal muscle atlas demonstrate its capability in generating accurate multimodal co-embeddings and discovering cellular identity.
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