Nature BiotechnologyBioinformaticsPeer-reviewed journal article
TACCO: Unified annotation transfer and decomposition of cell identities for single-cell and spatial omics
Simon MagesiD, Noa MorieliD, Inbal Avraham‐DavidiiD, Evan M. MurrayiD, Jan WatteriD, Fei CheniD, Orit Rozenblatt–RoseniD, Johanna KlughammeriD, Aviv RegeviD, Mor NitzaniD
Abstract
Rapid advances in single-cell-, spatial-, and multi-omics, allow us to profile cellular ecosystems in tissues at unprecedented resolution, scale, and depth. However, both technical limitations, such as low spatial resolution and biological variations, such as continuous spectra of cell states, often render these data imperfect representations of cellular systems, best captured as continuous mixtures over cells or molecules. Based on this conceptual insight, we build a versatile framework, TACCO (Transfer of Annotations to Cells and their COmbinations) that extends an Optimal Transport-based core by different wrappers or boosters to annotate a wide variety of data. We apply TACCO to identify cell types and states, decipher spatio-molecular tissue structure at the cell and molecular level, and resolve differentiation trajectories. TACCO excels in speed, scalability, and adaptability, while successfully outperforming benchmarks across diverse synthetic and biological datasets. Along with highly optimized visualization and analysis functions, TACCO forms a comprehensive integrated framework for studies of high-dimensional, high-resolution biology.
- assay: scRNA-seq
- assay: spatial transcriptomics
- assay: multiome
- research focus: cell type annotation
- research focus: trajectory inference
- research focus: benchmarking
- approach: optimal transport
- approach: statistical model
- Citations
- 93
- FWCI
- 8.26
- Field percentile
- top 1%
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