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门控的终结?高维细胞计数数据自动分析简介。

The end of gating? An introduction to automated analysis of high dimensional cytometry data.

作者信息

Mair Florian, Hartmann Felix J, Mrdjen Dunja, Tosevski Vinko, Krieg Carsten, Becher Burkhard

机构信息

Institute of Experimental Immunology, University of Zurich, Zurich, Switzerland.

出版信息

Eur J Immunol. 2016 Jan;46(1):34-43. doi: 10.1002/eji.201545774. Epub 2015 Nov 30.

Abstract

Ever since its invention half a century ago, flow cytometry has been a major tool for single-cell analysis, fueling advances in our understanding of a variety of complex cellular systems, in particular the immune system. The last decade has witnessed significant technical improvements in available cytometry platforms, such that more than 20 parameters can be analyzed on a single-cell level by fluorescence-based flow cytometry. The advent of mass cytometry has pushed this limit up to, currently, 50 parameters. However, traditional analysis approaches for the resulting high-dimensional datasets, such as gating on bivariate dot plots, have proven to be inefficient. Although a variety of novel computational analysis approaches to interpret these datasets are already available, they have not yet made it into the mainstream and remain largely unknown to many immunologists. Therefore, this review aims at providing a practical overview of novel analysis techniques for high-dimensional cytometry data including SPADE, t-SNE, Wanderlust, Citrus, and PhenoGraph, and how these applications can be used advantageously not only for the most complex datasets, but also for standard 14-parameter cytometry datasets.

摘要

自半个世纪前发明以来,流式细胞术一直是单细胞分析的主要工具,推动了我们对各种复杂细胞系统,特别是免疫系统理解的进步。过去十年见证了现有流式细胞术平台的重大技术改进,以至于基于荧光的流式细胞术能够在单细胞水平上分析20多个参数。质谱流式细胞术的出现将这一限制提高到了目前的50个参数。然而,事实证明,对由此产生的高维数据集进行传统分析的方法,如在双变量点图上进行门控,效率低下。尽管已经有多种解释这些数据集的新型计算分析方法,但它们尚未成为主流,许多免疫学家对此仍然知之甚少。因此,本综述旨在提供高维流式细胞术数据新型分析技术的实用概述,包括SPADE、t-SNE、Wanderlust、Citrus和PhenoGraph,以及这些应用如何不仅能有效地用于最复杂的数据集,还能用于标准的14参数流式细胞术数据集。

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