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本文引用的文献

1
OMIP-010: a new 10-color monoclonal antibody panel for polychromatic immunophenotyping of small hematopoietic cell samples.OMIP-010:一种用于小造血细胞样本多色免疫表型分析的新型10色单克隆抗体组合。
Cytometry A. 2012 Jun;81(6):453-5. doi: 10.1002/cyto.a.22056. Epub 2012 Apr 24.
2
B cells with high side scatter parameter by flow cytometry correlate with inferior survival in diffuse large B-cell lymphoma.流式细胞术检测到高侧向散射参数的 B 细胞与弥漫性大 B 细胞淋巴瘤的不良生存相关。
Am J Clin Pathol. 2012 May;137(5):805-14. doi: 10.1309/AJCPGR8BG4JDVOWR.
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A deep profiler's guide to cytometry.细胞仪深入剖析指南
Trends Immunol. 2012 Jul;33(7):323-32. doi: 10.1016/j.it.2012.02.010. Epub 2012 Apr 2.
4
OMIP-009: Characterization of antigen-specific human T-cells.OMIP - 009:抗原特异性人类T细胞的特征分析。
Cytometry A. 2012 May;81(5):362-3. doi: 10.1002/cyto.a.22042. Epub 2012 Mar 21.
5
OMIP-005: Quality and phenotype of antigen-responsive rhesus macaque T cells.OMIP - 005:恒河猴抗原反应性T细胞的质量与表型
Cytometry A. 2012 May;81(5):360-1. doi: 10.1002/cyto.a.22008. Epub 2012 Mar 21.
6
OMIP-008: measurement of Th1 and Th2 cytokine polyfunctionality of human T cells.OMIP-008:人类 T 细胞 Th1 和 Th2 细胞因子多功能性的测量。
Cytometry A. 2012 Jun;81(6):450-2. doi: 10.1002/cyto.a.22035. Epub 2012 Mar 19.
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OMIP-007: phenotypic analysis of human natural killer cells.OMIP - 007:人类自然杀伤细胞的表型分析
Cytometry A. 2012 Jun;81(6):447-9. doi: 10.1002/cyto.a.22033. Epub 2012 Mar 12.
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Cytometry: today's technology and tomorrow's horizons.流式细胞术:今日的技术与明日的前景。
Methods. 2012 Jul;57(3):251-8. doi: 10.1016/j.ymeth.2012.02.009. Epub 2012 Feb 25.
9
Early immunologic correlates of HIV protection can be identified from computational analysis of complex multivariate T-cell flow cytometry assays.从复杂的多变量 T 细胞流式细胞术分析的计算分析中,可以确定与 HIV 保护相关的早期免疫学指标。
Bioinformatics. 2012 Apr 1;28(7):1009-16. doi: 10.1093/bioinformatics/bts082. Epub 2012 Feb 29.
10
Standardizing immunophenotyping for the Human Immunology Project.标准化人类免疫计划的免疫表型分析。
Nat Rev Immunol. 2012 Feb 17;12(3):191-200. doi: 10.1038/nri3158.

RchyOptimyx:流式细胞术的细胞层次优化。

RchyOptimyx: cellular hierarchy optimization for flow cytometry.

机构信息

Terry Fox Laboratory, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.

出版信息

Cytometry A. 2012 Dec;81(12):1022-30. doi: 10.1002/cyto.a.22209. Epub 2012 Oct 8.

DOI:10.1002/cyto.a.22209
PMID:23044634
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3726344/
Abstract

Analysis of high-dimensional flow cytometry datasets can reveal novel cell populations with poorly understood biology. Following discovery, characterization of these populations in terms of the critical markers involved is an important step, as this can help to both better understand the biology of these populations and aid in designing simpler marker panels to identify them on simpler instruments and with fewer reagents (i.e., in resource poor or highly regulated clinical settings). However, current tools to design panels based on the biological characteristics of the target cell populations work exclusively based on technical parameters (e.g., instrument configurations, spectral overlap, and reagent availability). To address this shortcoming, we developed RchyOptimyx (cellular hieraRCHY OPTIMization), a computational tool that constructs cellular hierarchies by combining automated gating with dynamic programming and graph theory to provide the best gating strategies to identify a target population to a desired level of purity or correlation with a clinical outcome, using the simplest possible marker panels. RchyOptimyx can assess and graphically present the trade-offs between marker choice and population specificity in high-dimensional flow or mass cytometry datasets. We present three proof-of-concept use cases for RchyOptimyx that involve 1) designing a panel of surface markers for identification of rare populations that are primarily characterized using their intracellular signature; 2) simplifying the gating strategy for identification of a target cell population; 3) identification of a non-redundant marker set to identify a target cell population.

摘要

分析高维流式细胞术数据集可以揭示具有未知生物学特性的新型细胞群体。在发现这些群体之后,对其涉及的关键标志物进行特征描述是一个重要的步骤,因为这有助于更好地理解这些群体的生物学特性,并有助于设计更简单的标记面板,以便在更简单的仪器上使用更少的试剂(即在资源匮乏或高度监管的临床环境中)来识别它们。然而,目前基于目标细胞群体生物学特征来设计面板的工具仅基于技术参数(例如,仪器配置、光谱重叠和试剂可用性)。为了解决这一缺点,我们开发了 RchyOptimyx(细胞层次结构优化),这是一种计算工具,通过将自动门控与动态规划和图论相结合,构建细胞层次结构,提供最佳的门控策略,以达到所需的纯度或与临床结果的相关性来识别目标群体,同时使用最简单的可能的标记面板。RchyOptimyx 可以评估和图形化呈现高维流式或质谱细胞术数据集中标记选择和群体特异性之间的权衡。我们提出了 RchyOptimyx 的三个概念验证用例,涉及 1)设计用于识别主要通过细胞内特征来表征的稀有群体的表面标记面板;2)简化用于识别目标细胞群体的门控策略;3)识别用于识别目标细胞群体的非冗余标记集。