| Literature DB >> 35449415 |
Romain Lopez1, Baoguo Li2, Hadas Keren-Shaul3, Pierre Boyeau1, Merav Kedmi3, David Pilzer3, Adam Jelinski2, Ido Yofe2, Eyal David2, Allon Wagner1, Can Ergen1, Yoseph Addadi3, Ofra Golani3, Franca Ronchese4, Michael I Jordan2,5, Ido Amit6, Nir Yosef7,8,9,10.
Abstract
Most spatial transcriptomics technologies are limited by their resolution, with spot sizes larger than that of a single cell. Although joint analysis with single-cell RNA sequencing can alleviate this problem, current methods are limited to assessing discrete cell types, revealing the proportion of cell types inside each spot. To identify continuous variation of the transcriptome within cells of the same type, we developed Deconvolution of Spatial Transcriptomics profiles using Variational Inference (DestVI). Using simulations, we demonstrate that DestVI outperforms existing methods for estimating gene expression for every cell type inside every spot. Applied to a study of infected lymph nodes and of a mouse tumor model, DestVI provides high-resolution, accurate spatial characterization of the cellular organization of these tissues and identifies cell-type-specific changes in gene expression between different tissue regions or between conditions. DestVI is available as part of the open-source software package scvi-tools ( https://scvi-tools.org ).Entities:
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Year: 2022 PMID: 35449415 DOI: 10.1038/s41587-022-01272-8
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 68.164