scholarly journals Image3C, a multimodal image-based and label independent integrative method for single-cell analysis

eLife ◽  
2021 ◽  
Vol 10 ◽  
Author(s):  
Alice Accorsi ◽  
Andrew C Box ◽  
Robert Peuß ◽  
Christopher Wood ◽  
Alejandro Sánchez Alvarado ◽  
...  

Image-based cell classification has become a common tool to identify phenotypic changes in cell populations. However, this methodology is limited to organisms possessing well characterized species-specific reagents (e.g., antibodies) that allow cell identification, clustering and convolutional neural network (CNN) training. In the absence of such reagents, the power of image-based classification has remained mostly off-limits to many research organisms. We have developed an image-based classification methodology we named Image3C (Image-Cytometry Cell Classification) that does not require species-specific reagents nor pre-existing knowledge about the sample. Image3C combines image-based flow cytometry with an unbiased, high-throughput cell cluster pipeline and CNN integration. Image3C exploits intrinsic cellular features and non-species-specific dyes to perform de novo cell composition analysis and to detect changes in cellular composition between different conditions. Therefore, Image3C expands the use of imaged-based analyses of cell population composition to research organisms in which detailed cellular phenotypes are unknown or for which species-specific reagents are not available.

2019 ◽  
Author(s):  
Alice Accorsi ◽  
Andrew C. Box ◽  
Robert Peuß ◽  
Christopher Wood ◽  
Alejandro Sánchez Alvarado ◽  
...  

AbstractImage-based cell classification has become a common tool to identify phenotypic changes in cell populations. However, this methodology is limited to organisms possessing well characterized species-specific reagents (e.g., antibodies) that allow cell identification, clustering and convolutional neural network (CNN) training. In the absence of such reagents, the power of image-based classification has remained mostly off-limits to many research organisms. We have developed an image-based classification methodology we named Image3C (Image-Cytometry Cell Classification) that does not require species-specific reagents nor pre-existing knowledge about the sample. Image3C combines image-based flow cytometry with an unbiased, high-throughput cell cluster pipeline and CNN integration. Image3C exploits intrinsic cellular features and non-species-specific dyes to perform de novo cell composition analysis and to detect changes in cellular composition between different conditions. Therefore, Image3C expands the use of imaged-based analyses of cell population composition to research organisms in which detailed cellular phenotypes are unknown or for which species-specific reagents are not available.Impact statementImage3C analyzes cell populations through image-based clustering and neural network training, which allows single-cell analysis in research organisms devoid of species-specific reagents or pre-existing knowledge on cell phenotypes.


2020 ◽  
Vol 53 (4) ◽  
pp. 473-491.e9 ◽  
Author(s):  
Yufeng Lu ◽  
Fion Shiau ◽  
Wenyang Yi ◽  
Suying Lu ◽  
Qian Wu ◽  
...  

2014 ◽  
Vol 4 (1) ◽  
Author(s):  
Nobuo Yoshimoto ◽  
Kenji Tatematsu ◽  
Masumi Iijima ◽  
Tomoaki Niimi ◽  
Andrés D. Maturana ◽  
...  

Cell ◽  
2012 ◽  
Vol 150 (2) ◽  
pp. 402-412 ◽  
Author(s):  
Jianbin Wang ◽  
H. Christina Fan ◽  
Barry Behr ◽  
Stephen R. Quake

2020 ◽  
Author(s):  
Jennifer N. Berger ◽  
Bridget Sanford ◽  
Abigail K. Kimball ◽  
Lauren M. Oko ◽  
Rachael E. Kaspar ◽  
...  

SUMMARYVirus infection is frequently characterized using bulk cell populations. How these findings correspond to infection in individual cells remains unclear. Here, we integrate high-dimensional single-cell approaches to quantify viral and host RNA and protein expression signatures using de novo infection with a well-characterized model gammaherpesvirus. While infected cells demonstrated genome-wide transcription, individual cells revealed pronounced variation in gene expression, with only 9 of 80 annotated viral open reading frames uniformly expressed in all cells, and a 1000-fold variation in viral RNA expression between cells. Single-cell analysis further revealed positive and negative gene correlations, many uniquely present in a subset of cells. Beyond variation in viral gene expression, individual cells demonstrated a pronounced, dichotomous signature in host gene expression, revealed by measuring host RNA abundance and post-translational protein modifications. These studies provide a resource for the high-dimensional analysis of virus infection, and a conceptual framework to define virus infection as the sum of virus and host responses at the single-cell level.HIGHLIGHTSCyTOF and scRNA-seq identify wide variation in gene expression between infected cells.Host RNA expression and post-translational modifications stratify virus infection.Single cell RNA analysis reveals new relationships in viral gene expression.Simultaneous measurement of virus and host defines distinct infection states.


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