1. Multimodal hierarchical classification of CITE-seq data delineates immune cell states across lineages and tissues.
- Author
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Caron DP, Specht WL, Chen D, Wells SB, Szabo PA, Jensen IJ, Farber DL, and Sims PA
- Subjects
- Humans, Cell Lineage genetics, Gene Expression Profiling methods, Sequence Analysis, RNA methods, T-Lymphocyte Subsets immunology, T-Lymphocyte Subsets classification, T-Lymphocyte Subsets metabolism, Single-Cell Analysis methods, Transcriptome
- Abstract
Single-cell RNA sequencing (scRNA-seq) is invaluable for profiling cellular heterogeneity and transcriptional states, but transcriptomic profiles do not always delineate subsets defined by surface proteins. Cellular indexing of transcriptomes and epitopes (CITE-seq) enables simultaneous profiling of single-cell transcriptomes and surface proteomes; however, accurate cell-type annotation requires a classifier that integrates multimodal data. Here, we describe multimodal classifier hierarchy (MMoCHi), a marker-based approach for accurate cell-type classification across multiple single-cell modalities that does not rely on reference atlases. We benchmark MMoCHi using sorted T lymphocyte subsets and annotate a cross-tissue human immune cell dataset. MMoCHi outperforms leading transcriptome-based classifiers and multimodal unsupervised clustering in its ability to identify immune cell subsets that are not readily resolved and to reveal subset markers. MMoCHi is designed for adaptability and can integrate annotation of cell types and developmental states across diverse lineages, samples, or modalities., Competing Interests: Declaration of interests The authors declare no competing interests., (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)
- Published
- 2025
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