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Quantitative assessment of cell population diversity in single-cell landscapes.
Liu, Qi; Herring, Charles A; Sheng, Quanhu; Ping, Jie; Simmons, Alan J; Chen, Bob; Banerjee, Amrita; Li, Wei; Gu, Guoqiang; Coffey, Robert J; Shyr, Yu; Lau, Ken S.
Afiliação
  • Liu Q; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
  • Herring CA; Center for Quantitative Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
  • Sheng Q; Epithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
  • Ping J; Program in Chemical and Physical Biology, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
  • Simmons AJ; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
  • Chen B; Center for Quantitative Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
  • Banerjee A; Department of Biostatistics, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
  • Li W; Center for Quantitative Sciences, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
  • Gu G; Epithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
  • Coffey RJ; Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
  • Shyr Y; Epithelial Biology Center, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
  • Lau KS; Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, Tennessee, United States of America.
PLoS Biol ; 16(10): e2006687, 2018 10.
Article em En | MEDLINE | ID: mdl-30346945
Single-cell RNA sequencing (scRNA-seq) has become a powerful tool for the systematic investigation of cellular diversity. As a number of computational tools have been developed to identify and visualize cell populations within a single scRNA-seq dataset, there is a need for methods to quantitatively and statistically define proportional shifts in cell population structures across datasets, such as expansion or shrinkage or emergence or disappearance of cell populations. Here we present sc-UniFrac, a framework to statistically quantify compositional diversity in cell populations between single-cell transcriptome landscapes. sc-UniFrac enables sensitive and robust quantification in simulated and experimental datasets in terms of both population identity and quantity. We have demonstrated the utility of sc-UniFrac in multiple applications, including assessment of biological and technical replicates, classification of tissue phenotypes and regional specification, identification and definition of altered cell infiltrates in tumorigenesis, and benchmarking batch-correction tools. sc-UniFrac provides a framework for quantifying diversity or alterations in cell populations across conditions and has broad utility for gaining insight into tissue-level perturbations at the single-cell resolution.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Sequência de RNA / Perfilação da Expressão Gênica / Análise de Célula Única Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Análise de Sequência de RNA / Perfilação da Expressão Gênica / Análise de Célula Única Limite: Animals / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article