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protGear:一种蛋白质微阵列数据预处理套件。

protGear: A protein microarray data pre-processing suite.

作者信息

Mwai Kennedy, Kibinge Nelson, Tuju James, Kamuyu Gathoni, Kimathi Rinter, Mburu James, Chepsat Emily, Nyamako Lydia, Chege Timothy, Nkumama Irene, Kinyanjui Samson, Musenge Eustasius, Osier Faith

机构信息

Epidemiology and Biostatistics Division, School of Public Health, University of the Witwatersrand, Johannesburg, South Africa.

Centre for Geographic Medicine Research (Coast), Kenya Medical Research Institute-Wellcome Trust Research Programme, Kilifi, Kenya.

出版信息

Comput Struct Biotechnol J. 2021 Apr 24;19:2518-2525. doi: 10.1016/j.csbj.2021.04.044. eCollection 2021.

Abstract

Protein microarrays are versatile tools for high throughput study of the human proteome, but systematic and non-systematic sources of bias constrain optimal interpretation and the ultimate utility of the data. Published guidelines to limit technical variability whilst maintaining important biological variation favour DNA-based microarrays that often differ fundamentally in their experimental design. Rigorous tools to guide background correction, the quantification of within-sample variation, normalisation, and batch correction specifically for protein microarrays are limited, require extensive investigation and are not centrally accessible. Here, we develop a generic one-stop-shop pre-processing suite for protein microarrays that is compatible with data from the major protein microarray scanners. Our graphical and tabular interfaces facilitate a detailed inspection of data and are coupled with supporting guidelines that enable users to select the most appropriate algorithms to systematically address bias arising in customized experiments. The localization and distribution of background signal intensities determine the optimal correction strategy. A novel function overcomes the limitations in the interpretation of the coefficient of variation when signal intensities are at the lower end of the detection threshold. We demonstrate essential considerations in the experimental design and their impact on a range of algorithms for normalization and minimization of batch effects. Our user-friendly interactive web-based platform eliminates the need for prowess in programming. The open-source R interface includes illustrative examples, generates an auditable record, enables reproducibility, and can incorporate additional custom scripts through its online repository. This versatility will enhance its broad uptake in the infectious disease and vaccine development community.

摘要

蛋白质微阵列是用于人类蛋白质组高通量研究的多功能工具,但系统和非系统的偏差来源限制了对数据的最佳解读及其最终效用。已发布的在限制技术变异性的同时保持重要生物学变异的指南倾向于基于DNA的微阵列,而这些微阵列在实验设计上往往有根本差异。专门针对蛋白质微阵列指导背景校正、样本内变异量化、归一化和批次校正的严格工具有限,需要大量研究且无法集中获取。在此,我们开发了一个通用的一站式蛋白质微阵列预处理套件,它与主要蛋白质微阵列扫描仪的数据兼容。我们的图形和表格界面便于对数据进行详细检查,并配有支持性指南,使用户能够选择最合适的算法,以系统地解决定制实验中出现的偏差。背景信号强度的定位和分布决定了最佳校正策略。当信号强度处于检测阈值下限的时候,一种新颖的功能克服了变异系数解释方面的局限性。我们展示了实验设计中的重要考虑因素及其对一系列归一化算法和批次效应最小化算法的影响。我们用户友好的基于网络的交互式平台消除了对编程技能的需求。开源的R接口包含示例,生成可审计记录,实现可重复性,并且可以通过其在线存储库纳入额外的自定义脚本。这种多功能性将提高其在传染病和疫苗开发领域的广泛应用。

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