Nature CommunicationsBioinformaticsPeer-reviewed journal article
GeneVector: Identification of transcriptional programs using dense vector representations defined by mutual information.
Nicholas CegliaiD, Zachary M. SethnaiD, Samuel S. FreemaniD, Florian UhlitziD, Viktoria BojilovaiD, Nicole RuskiD, Bharat BurmaniD, Andrew T. ChowiD, Sohrab SalehiiD, Farhia KabeeriD, Samuel A. J. R. AparicioiD, Benjamin D. GreenbaumiD, Sohrab P. ShahiD, Andrew McPhersoniD
Abstract
Deciphering individual cell phenotypes from cell-specific transcriptional processes requires high dimensional single cell RNA sequencing. However, current dimensionality reduction methods aggregate sparse gene information across cells, without directly measuring the relationships that exist between genes. By performing dimensionality reduction with respect to gene co-expression, low-dimensional features can model these gene-specific relationships and leverage shared signal to overcome sparsity. We describe GeneVector, a scalable framework for dimensionality reduction implemented as a vector space model using mutual information between gene expression. Unlike other methods, including principal component analysis and variational autoencoders, GeneVector uses latent space arithmetic in a lower dimensional gene embedding to identify transcriptional programs and classify cell types. In this work, we show in four single cell RNA-seq datasets that GeneVector was able to capture phenotypespecific pathways, perform batch effect correction, interactively annotate cell types, and identify pathway variation with treatment over time.
- assay: scRNA-seq
- research focus: dimensionality reduction
- research focus: cell type annotation
- research focus: batch correction / integration
- research focus: differential expression
- approach: statistical model
- approach: matrix factorization
- Citations
- 10
- FWCI
- 0.71
- Field percentile
- top 36%
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