多路复用成像数据处理 FAIR 质量控制透视

Wouter‐Michiel A.M. Vierdag, Sinem K. Saka
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引用次数: 0

摘要

多重成像方法越来越多地被用于大面积组织的成像,从而产生了大量的成像数据集,包括样本数量和每个样本的图像数据大小。为了简化对多重成像的分析,人们开发了利用最先进算法的自动流水线。在这些流水线中,一个处理步骤的输出质量通常取决于前一个步骤的输出,每个步骤的误差,即使看起来很小,也会传播并混淆结果。因此,在图像处理管道的每个不同步骤中进行严格的质量控制(QC),对于正确分析和解释分析结果以及确保数据的可重用性都至关重要。在理想情况下,质量控制应成为成像数据集和分析流程中不可分割且易于检索的一部分。然而,由于目前可用框架的局限性,对于大型多重成像数据来说,整合交互式质量控制非常困难。鉴于多路复用成像数据集的规模和复杂性不断增加,我们提出了在图像分析管道中集成质量控制所面临的不同挑战,并在生物图像分析最新进展的基础上提出了可能的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A perspective on FAIR quality control in multiplexed imaging data processing
Multiplexed imaging approaches are getting increasingly adopted for imaging of large tissue areas, yielding big imaging datasets both in terms of the number of samples and the size of image data per sample. The processing and analysis of these datasets is complex owing to frequent technical artifacts and heterogeneous profiles from a high number of stained targets To streamline the analysis of multiplexed images, automated pipelines making use of state-of-the-art algorithms have been developed. In these pipelines, the output quality of one processing step is typically dependent on the output of the previous step and errors from each step, even when they appear minor, can propagate and confound the results. Thus, rigorous quality control (QC) at each of these different steps of the image processing pipeline is of paramount importance both for the proper analysis and interpretation of the analysis results and for ensuring the reusability of the data. Ideally, QC should become an integral and easily retrievable part of the imaging datasets and the analysis process. Yet, limitations of the currently available frameworks make integration of interactive QC difficult for large multiplexed imaging data. Given the increasing size and complexity of multiplexed imaging datasets, we present the different challenges for integrating QC in image analysis pipelines as well as suggest possible solutions that build on top of recent advances in bioimage analysis.
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