Comparison of three machine learning algorithms for classification of B-cell neoplasms using clinical flow cytometry data

IF 2.3 3区 医学 Q3 MEDICAL LABORATORY TECHNOLOGY Cytometry Part B: Clinical Cytometry Pub Date : 2024-05-09 DOI:10.1002/cyto.b.22177
Wikum Dinalankara, David P. Ng, Luigi Marchionni, Paul D. Simonson
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Abstract

Multiparameter flow cytometry data is visually inspected by expert personnel as part of standard clinical disease diagnosis practice. This is a demanding and costly process, and recent research has demonstrated that it is possible to utilize artificial intelligence (AI) algorithms to assist in the interpretive process. Here we report our examination of three previously published machine learning methods for classification of flow cytometry data and apply these to a B-cell neoplasm dataset to obtain predicted disease subtypes. Each of the examined methods classifies samples according to specific disease categories using ungated flow cytometry data. We compare and contrast the three algorithms with respect to their architectures, and we report the multiclass classification accuracies and relative required computation times. Despite different architectures, two of the methods, flowCat and EnsembleCNN, had similarly good accuracies with relatively fast computational times. We note a speed advantage for EnsembleCNN, particularly in the case of addition of training data and retraining of the classifier.

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利用临床流式细胞仪数据对三种机器学习算法进行 B 细胞肿瘤分类的比较。
作为标准临床疾病诊断实践的一部分,专家要对多参数流式细胞仪数据进行目视检查。这是一个要求严格且成本高昂的过程,最近的研究表明,利用人工智能(AI)算法协助解释过程是可行的。在此,我们报告了对之前发表的三种流式细胞仪数据分类机器学习方法的研究,并将这些方法应用于B细胞肿瘤数据集,以获得预测的疾病亚型。所研究的每种方法都能利用非门控流式细胞仪数据根据特定疾病类别对样本进行分类。我们对三种算法的架构进行了比较和对比,并报告了多类分类的准确性和所需的相对计算时间。尽管架构不同,但其中的两种方法,即 flowCat 和 EnsembleCNN,都具有类似的高准确度和相对较短的计算时间。我们注意到 EnsembleCNN 的速度优势,特别是在增加训练数据和重新训练分类器的情况下。
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来源期刊
CiteScore
6.80
自引率
32.40%
发文量
51
审稿时长
>12 weeks
期刊介绍: Cytometry Part B: Clinical Cytometry features original research reports, in-depth reviews and special issues that directly relate to and palpably impact clinical flow, mass and image-based cytometry. These may include clinical and translational investigations important in the diagnostic, prognostic and therapeutic management of patients. Thus, we welcome research papers from various disciplines related [but not limited to] hematopathologists, hematologists, immunologists and cell biologists with clinically relevant and innovative studies investigating individual-cell analytics and/or separations. In addition to the types of papers indicated above, we also welcome Letters to the Editor, describing case reports or important medical or technical topics relevant to our readership without the length and depth of a full original report.
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