bioRxivBioinformaticsPreprint
PHLOWER - Single cell trajectory analysis using Decomposition of the Hodge Laplacian
Mingbo ChengiD, Jitske JanseniD, Katharina C. ReimeriD, Vincent GrandeiD, James Shiniti NagaiiD, Zhijian LiiD, Paul KießlingiD, Martin GraßhoffiD, Christoph KuppeiD, Michael T. SchaubiD, Rafael KramanniD, Ivan G. CostaiD
Abstract
Multi-modal single-cell sequencing, which captures changes in chromatin and gene expression in the same cells, is a game changer in the study of gene regulation in cellular differentiation processes. Computational trajectory analysis is a key computational task for inferring differentiation trees from this single-cell data, though current methods struggle with complex, multi-branching trees and multi-modal data. To address this, PHLOWER (decomPosition of the Hodge Laplacian for inferring trajectOries from floWs of cEll diffeRentiation) leverages the harmonic component of the Hodge decomposition on simplicial complexes to infer trajectory embeddings. These natural representations of cell differentiation facilitate the estimation of their underlying differentiation trees. We evaluate PHLOWER through benchmarking with multi-branching differentiation trees and using novel kidney organoid multi-modal and spatial single-cell data. These demonstrate the power of PHLOWER in both the inference of complex trees and the identification of transcription factors regulating off-target cells in kidney organoids.
- organism: human
- assay: scRNA-seq
- assay: spatial transcriptomics
- research focus: trajectory inference
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: statistical model
- Citations
- 0
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