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Bi-order multimodal integration of single-cell data.

Jinzhuang DouShaoheng LiangVakul MohantyQi MiaoYuefan HuangQingnan LiangXuesen ChengSangbae KimJongsu ChoiYumei LiLi LiMay DaherRafet BasarKatayoun RezvaniRui ChenKen Chen
Published in: Genome biology (2022)
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.
Keyphrases
  • single cell
  • rna seq
  • high throughput
  • electronic health record
  • big data
  • pain management
  • skeletal muscle
  • machine learning
  • artificial intelligence