Automated image registration of RGB, hyperspectral and chlorophyll fluorescence imaging data.

IF 4.7 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Hans Lukas Bethge, Inga Weisheit, Mauritz Sandro Dortmund, Timm Landes, Miroslav Zabic, Marcus Linde, Thomas Debener, Dag Heinemann
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引用次数: 0

Abstract

Background: The early and specific detection of abiotic and biotic stresses, particularly their combinations, is a major challenge for maintaining and increasing plant productivity in sustainable agriculture under changing environmental conditions. Optical imaging techniques enable cost-efficient and non-destructive quantification of plant stress states. Monomodal detection of certain stressors is usually based on non-specific/indirect features and therefore is commonly limited in their cross-specificity to other stressors. The fusion of multi-domain sensor systems can provide more potentially discriminative features for machine learning models and potentially provide synergistic information to increase cross-specificity in plant disease detection when image data are fused at the pixel level.

Results: In this study, we demonstrate successful multi-modal image registration of RGB, hyperspectral (HSI) and chlorophyll fluorescence (ChlF) kinetics data at the pixel level for high-throughput phenotyping of A. thaliana grown in Multi-well plates and an assay with detached leaf discs of Rosa × hybrida inoculated with the black spot disease-inducing fungus Diplocarpon rosae. Here, we showcase the effects of (i) selection of reference image selection, (ii) different registrations methods and (iii) frame selection on the performance of image registration via affine transform. In addition, we developed a combined approach for registration methods through NCC-based selection for each file, resulting in a robust and accurate approach that sacrifices computational time. Since image data encompass multiple objects, the initial coarse image registration using a global transformation matrix exhibited heterogeneity across different image regions. By employing an additional fine registration on the object-separated image data, we achieved a high overlap ratio. Specifically, for the A. thaliana test set, the overlap ratios (ORConvex) were 98.0 ± 2.3% for RGB-to-ChlF and 96.6 ± 4.2% for HSI-to-ChlF. For the Rosa × hybrida test set, the values were 98.9 ± 0.5% for RGB-to-ChlF and 98.3 ± 1.3% for HSI-to-ChlF.

Conclusion: The presented multi-modal imaging pipeline enables high-throughput, high-dimensional phenotyping of different plant species with respect to various biotic or abiotic stressors. This paves the way for in-depth studies investigating the correlative relationships of the multi-domain data or the performance enhancement of machine learning models via multi modal image fusion.

RGB、高光谱和叶绿素荧光成像数据的自动图像注册。
背景:在不断变化的环境条件下,要保持和提高可持续农业中的植物生产力,就必须及早具体地检测非生物和生物胁迫,特别是它们的组合。光学成像技术可对植物胁迫状态进行低成本、无损的量化。对某些胁迫的单模式检测通常基于非特异性/间接特征,因此对其他胁迫的交叉特异性通常有限。多域传感器系统的融合可为机器学习模型提供更多潜在的鉴别特征,并有可能提供协同信息,从而在像素级融合图像数据时提高植物病害检测的交叉特异性:在本研究中,我们展示了在像素级成功实现 RGB、高光谱(HSI)和叶绿素荧光(ChlF)动力学数据的多模式图像配准,用于多孔板中生长的大叶黄杨的高通量表型分析,以及接种了黑斑病诱导真菌 Diplocarpon rosae 的蔷薇×杂交种分离叶盘的检测。在此,我们展示了(i) 参考图像选择、(ii) 不同注册方法和(iii) 帧选择对通过仿射变换进行图像注册的性能的影响。此外,我们还通过基于 NCC 的选择为每个文件开发了一种组合注册方法,从而在牺牲计算时间的情况下实现了稳健而精确的方法。由于图像数据包含多个对象,使用全局变换矩阵进行的初始粗略图像配准在不同图像区域之间表现出异质性。通过对对象分离的图像数据进行额外的精细配准,我们实现了较高的重叠率。具体来说,在大丽花测试集中,RGB-to-ChlF 的重叠率(ORConvex)为 98.0 ± 2.3%,HSI-to-ChlF 的重叠率(ORConvex)为 96.6 ± 4.2%。对于 Rosa × hybrida 测试集,RGB-to-ChlF 的比值为 98.9 ± 0.5%,HSI-to-ChlF 的比值为 98.3 ± 1.3%:所介绍的多模式成像管道可针对各种生物或非生物胁迫因素,对不同植物物种进行高通量、高维表型分析。这为深入研究多域数据的相关关系或通过多模态图像融合提高机器学习模型的性能铺平了道路。
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来源期刊
Plant Methods
Plant Methods 生物-植物科学
CiteScore
9.20
自引率
3.90%
发文量
121
审稿时长
2 months
期刊介绍: Plant Methods is an open access, peer-reviewed, online journal for the plant research community that encompasses all aspects of technological innovation in the plant sciences. There is no doubt that we have entered an exciting new era in plant biology. The completion of the Arabidopsis genome sequence, and the rapid progress being made in other plant genomics projects are providing unparalleled opportunities for progress in all areas of plant science. Nevertheless, enormous challenges lie ahead if we are to understand the function of every gene in the genome, and how the individual parts work together to make the whole organism. Achieving these goals will require an unprecedented collaborative effort, combining high-throughput, system-wide technologies with more focused approaches that integrate traditional disciplines such as cell biology, biochemistry and molecular genetics. Technological innovation is probably the most important catalyst for progress in any scientific discipline. Plant Methods’ goal is to stimulate the development and adoption of new and improved techniques and research tools and, where appropriate, to promote consistency of methodologies for better integration of data from different laboratories.
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