High throughput automated analysis of big flow cytometry data

被引:25
|
作者
Rahim, Albina [1 ,7 ]
Meskas, Justin [1 ]
Drissler, Sibyl [1 ]
Yue, Alice [1 ,5 ]
Lorenc, Anna [2 ]
Laing, Adam [2 ]
Saran, Namita [2 ]
White, Jacqui [3 ]
Abeler-Dorner, Lucie [2 ]
Hayday, Adrian [2 ,4 ]
Brinkman, Ryan R. [1 ,6 ]
机构
[1] British Columbia Canc Agcy, Terry Fox Lab, Vancouver, BC, Canada
[2] Kings Coll London, Dept Immunobiol, London, England
[3] Wellcome Trust Sanger Inst, Hinxton, England
[4] Francis Crick Inst, London, England
[5] Simon Fraser Univ, Sch Comp Sci, Burnaby, BC, Canada
[6] Univ British Columbia, Dept Med Genet, Vancouver, BC, Canada
[7] Univ British Columbia, Dept Bioinformat, Vancouver, BC, Canada
基金
英国惠康基金; 加拿大自然科学与工程研究理事会;
关键词
Flow cytometry; Automated analysis; Bioinformatics; COMPUTATIONAL ANALYSIS; CELL-POPULATIONS; IDENTIFICATION; BIOCONDUCTOR; DISCOVERY;
D O I
10.1016/j.ymeth.2017.12.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The rapid expansion of flow cytometry applications has outpaced the functionality of traditional manual analysis tools used to interpret flow cytometry data. Scientists are faced with the daunting prospect of manually identifying interesting cell populations in 50-dimensional datasets, equalling the complexity previously only reached in mass cytometry. Data can no longer be analyzed or interpreted fully by manual approaches. While automated gating has been the focus of intense efforts, there are many significant additional steps to the analytical pipeline (e.g., cleaning the raw files, event outlier detection, extracting immunophenotypes). We review the components of a customized automated analysis pipeline that can be generally applied to large scale flow cytometry data. We demonstrate these methodologies on data collected by the International Mouse Phenotyping Consortium (IMPC). Crown Copyright (C) 2017 Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:164 / 176
页数:13
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