转录组
反褶积
计算生物学
电池类型
推论
计算机科学
生物
空间分析
基因表达
基因
细胞
数据挖掘
人工智能
遗传学
算法
数学
统计
作者
Romain Lopez,Baoguo Li,Hadas Keren‐Shaul,Pierre Boyeau,Merav Kedmi,David Pilzer,Adam Jelinski,Ido Yofe,Eyal David,Allon Wagner,Can Ergen,Yoseph Addadi,Ofra Golani,Franca Ronchese,Michael I. Jordan,Ido Amit,Nir Yosef
标识
DOI:10.1038/s41587-022-01272-8
摘要
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 ). DestVI models continuous cell states in spatial transcriptomics data.
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