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Combining Multiple Annotations to Count Cells in 3D Cardiovascular Immunofluorescent Images

机译:将多个注释组合到3D心血管免疫荧光图像中的单元格计数

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Cell quantification in 3D atherosclerotic plaque immunofluorescent images is critical in improving understanding of plaque composition and possibly preventing rupture. Manual annotation of these cells is required to build predictive models that classify cell types within the lesion. Due to the difficulty and the amount of time required to label a substantial number of cells, researchers must often aggregate multiple annotation strategies with various limitations. We present several methods to create segmentation masks to include polygon outlines, basic shapes, and small dots. The combination of these methods leverages the nuclei polygon annotations that must be linked to the other cellular markers. A U-Net segmentation model was trained with these annotations and used for evaluation. The models achieved a test set total cell count percent error of -2.7 when assessing total cell count alone; and 5.3, and 1.4 when counting ACTA2+ or LGALS3+ cells respectively. Further analysis of these cell counts with patient phenotype data may lead to findings that ultimately reduce heart attack and stroke rates.
机译:3D动脉粥样硬化斑块免疫荧光图像中的细胞定量对于改善对斑块组成的理解以及可能预防破裂的关键。手动注释这些单元格需要构建在病变内分类细胞类型的预测模型。由于标记大量细胞所需的困难和时间所需的时间,研究人员必须汇总具有各种限制的多个注释策略。我们提出了几种方法来创建分段掩模,包括多边形轮廓,基本形状和小点。这些方法的组合利用必须与其他细胞标记连接的核多边形注释。使用这些注释培训U-Net分段模型并用于评估。当单独评估总细胞计数时,该模型达到了-2.7的总细胞计数百分比误差;分别计算Acta2 +或LGALS3 +细胞时5.3和1.4。对具有患者表型数据的这些细胞计数的进一步分析可能导致最终降低心脏病发作和行程率的结果。

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