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鉴定非均匀神经元图像中的弱信号,以实现稀疏分布神经突的大规模追踪。

Identifying Weak Signals in Inhomogeneous Neuronal Images for Large-Scale Tracing of Sparsely Distributed Neurites.

机构信息

Britton Chance Center for Biomedical Photonics, Wuhan National Laboratory for Optoelectronics-Huazhong University of Science and Technology, Wuhan, 430074, Hubei, China.

MOE Key Laboratory for Biomedical Photonics, Collaborative Innovation Center for Biomedical Engineering, School of Engineering Sciences, Huazhong University of Science and Technology, Wuhan, 430074, Hubei, China.

出版信息

Neuroinformatics. 2019 Oct;17(4):497-514. doi: 10.1007/s12021-018-9414-9.

DOI:10.1007/s12021-018-9414-9
PMID:30635864
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6841657/
Abstract

Tracing neurites constitutes the core of neuronal morphology reconstruction, a key step toward neuronal circuit mapping. Modern optical-imaging techniques allow observation of nearly complete mouse neuron morphologies across brain regions or even the whole brain. However, high-level automation reconstruction of neurons, i.e., the reconstruction with a few of manual edits requires discrimination of weak foreground points from the inhomogeneous background. We constructed an identification model, where empirical observations made from neuronal images were summarized into rules for designing feature vectors that to classify foreground and background, and a support vector machine (SVM) was used to learn these feature vectors. We embedded this constructed SVM classifier into a previously developed tool, SparseTracer, to obtain SparseTracer-Learned Feature Vector (ST-LFV). ST-LFV can trace sparsely distributed neurites with weak signals (contrast-to-noise ratio < 1.5) against an inhomogeneous background in datasets imaged by widely used light-microscopy techniques like confocal microscopy and two-photon microscopy. Moreover, 12 sub-blocks were extracted from different brain regions. The average recall and precision rates were 99% and 97%, respectively. These results indicated that ST-LFV is well suited for weak signal identification with varying image characteristics. We also applied ST-LFV to trace long-range neurites from images where neurites are sparsely distributed but their image intensities are weak in some cases. When tracing this long-range neurites, manual edit was required once to obtain results equivalent to the ground truth, compared with 20 times of manual edits required by SparseTracer. This improvement in the level of automatic reconstruction indicates that ST-LFV has the potential to rapidly reconstruct sparsely distributed neurons at the large scale.

摘要

追踪神经突是神经元形态重建的核心,这是神经元回路映射的关键步骤。现代光学成像技术允许观察到整个大脑甚至整个大脑区域的近完整的小鼠神经元形态。然而,神经元的高级自动化重建,即只需要少量手动编辑的重建,需要从不均匀的背景中区分出弱的前景点。我们构建了一个识别模型,其中从神经元图像中得出的经验观察结果被总结为用于设计特征向量的规则,用于对前景和背景进行分类,并且支持向量机(SVM)用于学习这些特征向量。我们将这个构建的 SVM 分类器嵌入到一个先前开发的工具中,即稀疏追踪器,以获得稀疏追踪器学习的特征向量(ST-LFV)。ST-LFV 可以在使用共聚焦显微镜和双光子显微镜等广泛使用的光显微镜技术成像的数据集中标记弱信号(对比度噪声比<1.5)和不均匀背景下稀疏分布的神经突。此外,从不同的脑区提取了 12 个子块。平均召回率和精度率分别为 99%和 97%。这些结果表明,ST-LFV 非常适合具有不同图像特征的弱信号识别。我们还将 ST-LFV 应用于追踪长距离神经突的图像,这些图像中的神经突分布稀疏,但在某些情况下其图像强度较弱。在追踪这些长距离神经突时,与稀疏追踪器需要 20 次手动编辑才能获得与真实值等效的结果相比,仅需要进行一次手动编辑即可获得结果。这种自动重建水平的提高表明,ST-LFV 有可能快速重建大规模稀疏分布的神经元。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/2cad5ad87995/12021_2018_9414_Fig12_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/9fc422801c0b/12021_2018_9414_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/2cad5ad87995/12021_2018_9414_Fig12_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/85c54ee82563/12021_2018_9414_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/7b9bbc2b05ac/12021_2018_9414_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/6b1ddc355e1c/12021_2018_9414_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/6cbcaf3dbb39/12021_2018_9414_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/bae4124cb4f4/12021_2018_9414_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/44e6b4a4bee5/12021_2018_9414_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/e000bb55f266/12021_2018_9414_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/bd9224ed4420/12021_2018_9414_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/b1cbcc022adf/12021_2018_9414_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/1bdd1c707249/12021_2018_9414_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/9fc422801c0b/12021_2018_9414_Fig11_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a8b4/6841657/2cad5ad87995/12021_2018_9414_Fig12_HTML.jpg

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