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{"title":"Generating Quantitative Cell Identity Labels with Marker Enrichment Modeling (MEM)","authors":"Kirsten E. Diggins, Jocelyn S. Gandelman, Caroline E. Roe, Jonathan M. Irish","doi":"10.1002/cpcy.34","DOIUrl":null,"url":null,"abstract":"<p>Multiplexed single-cell experimental techniques like mass cytometry measure 40 or more features and enable deep characterization of well-known and novel cell populations. However, traditional data analysis techniques rely extensively on human experts or prior knowledge, and novel machine learning algorithms may generate unexpected population groupings. Marker enrichment modeling (MEM) creates quantitative identity labels based on features enriched in a population relative to a reference. While developed for cell type analysis, MEM labels can be generated for a wide range of multidimensional data types, and MEM works effectively with output from expert analysis and diverse machine learning algorithms. MEM is implemented as an R package and includes three steps: (1) calculation of MEM values that quantify each feature's relative enrichment in the population, (2) reporting of MEM labels as a heatmap or as a text label, and (3) quantification of MEM label similarity between populations. The protocols here show MEM analysis using datasets from immunology and oncology. These MEM implementations provide a way to characterize population identity and novelty in the context of computational and expert analyses. © 2018 by John Wiley & Sons, Inc.</p>","PeriodicalId":11020,"journal":{"name":"Current Protocols in Cytometry","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2018-01-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpcy.34","citationCount":"20","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Cytometry","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpcy.34","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Health Professions","Score":null,"Total":0}
引用次数: 20
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Abstract
Multiplexed single-cell experimental techniques like mass cytometry measure 40 or more features and enable deep characterization of well-known and novel cell populations. However, traditional data analysis techniques rely extensively on human experts or prior knowledge, and novel machine learning algorithms may generate unexpected population groupings. Marker enrichment modeling (MEM) creates quantitative identity labels based on features enriched in a population relative to a reference. While developed for cell type analysis, MEM labels can be generated for a wide range of multidimensional data types, and MEM works effectively with output from expert analysis and diverse machine learning algorithms. MEM is implemented as an R package and includes three steps: (1) calculation of MEM values that quantify each feature's relative enrichment in the population, (2) reporting of MEM labels as a heatmap or as a text label, and (3) quantification of MEM label similarity between populations. The protocols here show MEM analysis using datasets from immunology and oncology. These MEM implementations provide a way to characterize population identity and novelty in the context of computational and expert analyses. © 2018 by John Wiley & Sons, Inc.
利用标记富集模型(Marker Enrichment Modeling, MEM)生成定量细胞身份标签。
多路单细胞实验技术,如质量细胞术,可以测量40个或更多的特征,并能够深入表征已知的和新的细胞群。然而,传统的数据分析技术广泛依赖于人类专家或先验知识,而新的机器学习算法可能会产生意想不到的人口分组。标记富集建模(Marker enrichment modeling, MEM)基于种群中相对于参考的富集特征创建定量的身份标签。虽然是为细胞类型分析而开发的,但MEM标签可以为广泛的多维数据类型生成,并且MEM可以有效地与专家分析和各种机器学习算法的输出一起工作。MEM作为一个R包实现,包括三个步骤:(1)计算MEM值,量化每个特征在种群中的相对富集程度;(2)将MEM标签报告为热图或文本标签;(3)量化种群之间的MEM标签相似性。这里的方案显示了使用免疫学和肿瘤学数据集的MEM分析。这些MEM实现提供了一种在计算和专家分析的背景下表征群体身份和新颖性的方法。©2018 by John Wiley & Sons, Inc。
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