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De novo gene signature identification from single‐cell RNA ‐seq with hierarchical Poisson factorization
Author(s) -
Levitin Hanna Mendes,
Yuan Jinzhou,
Cheng Yim Ling,
Ruiz Francisco JR,
Bush Erin C,
Bruce Jeffrey N,
Canoll Peter,
Iavarone Antonio,
Lasorella Anna,
Blei David M,
Sims Peter A
Publication year - 2019
Publication title -
molecular systems biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 8.523
H-Index - 148
ISSN - 1744-4292
DOI - 10.15252/msb.20188557
Subject(s) - columbia university , library science , biology , sociology , computer science , media studies
Common approaches to gene signature discovery in single‐cell RNA ‐sequencing (sc RNA ‐seq) depend upon predefined structures like clusters or pseudo‐temporal order, require prior normalization, or do not account for the sparsity of single‐cell data. We present single‐cell hierarchical Poisson factorization (sc HPF ), a Bayesian factorization method that adapts hierarchical Poisson factorization (Gopalan et al , [Gopalan P, 2015], Proceedings of the 31st Conference on Uncertainty in Artificial Intelligence , 326) for de novo discovery of both continuous and discrete expression patterns from sc RNA ‐seq. sc HPF does not require prior normalization and captures statistical properties of single‐cell data better than other methods in benchmark datasets. Applied to sc RNA ‐seq of the core and margin of a high‐grade glioma, sc HPF uncovers marked differences in the abundance of glioma subpopulations across tumor regions and regionally associated expression biases within glioma subpopulations. sc HFP revealed an expression signature that was spatially biased toward the glioma‐infiltrated margins and associated with inferior survival in glioblastoma.

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