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Segmentation-Less, Automated, Vascular Vectorization.
Mihelic, Samuel A; Sikora, William A; Hassan, Ahmed M; Williamson, Michael R; Jones, Theresa A; Dunn, Andrew K.
Afiliação
  • Mihelic SA; Department of Biomedical Engineering, The University of Texas, Austin, Texas, United States of America.
  • Sikora WA; Department of Biomedical Engineering, The University of Texas, Austin, Texas, United States of America.
  • Hassan AM; Department of Biomedical Engineering, The University of Texas, Austin, Texas, United States of America.
  • Williamson MR; Institute for Neuroscience, The University of Texas, Austin, Texas, United States of America.
  • Jones TA; Institute for Neuroscience, The University of Texas, Austin, Texas, United States of America.
  • Dunn AK; Department of Biomedical Engineering, The University of Texas, Austin, Texas, United States of America.
PLoS Comput Biol ; 17(10): e1009451, 2021 10.
Article em En | MEDLINE | ID: mdl-34624013
Recent advances in two-photon fluorescence microscopy (2PM) have allowed large scale imaging and analysis of blood vessel networks in living mice. However, extracting network graphs and vector representations for the dense capillary bed remains a bottleneck in many applications. Vascular vectorization is algorithmically difficult because blood vessels have many shapes and sizes, the samples are often unevenly illuminated, and large image volumes are required to achieve good statistical power. State-of-the-art, three-dimensional, vascular vectorization approaches often require a segmented (binary) image, relying on manual or supervised-machine annotation. Therefore, voxel-by-voxel image segmentation is biased by the human annotator or trainer. Furthermore, segmented images oftentimes require remedial morphological filtering before skeletonization or vectorization. To address these limitations, we present a vectorization method to extract vascular objects directly from unsegmented images without the need for machine learning or training. The Segmentation-Less, Automated, Vascular Vectorization (SLAVV) source code in MATLAB is openly available on GitHub. This novel method uses simple models of vascular anatomy, efficient linear filtering, and vector extraction algorithms to remove the image segmentation requirement, replacing it with manual or automated vector classification. Semi-automated SLAVV is demonstrated on three in vivo 2PM image volumes of microvascular networks (capillaries, arterioles and venules) in the mouse cortex. Vectorization performance is proven robust to the choice of plasma- or endothelial-labeled contrast, and processing costs are shown to scale with input image volume. Fully-automated SLAVV performance is evaluated on simulated 2PM images of varying quality all based on the large (1.4×0.9×0.6 mm3 and 1.6×108 voxel) input image. Vascular statistics of interest (e.g. volume fraction, surface area density) calculated from automatically vectorized images show greater robustness to image quality than those calculated from intensity-thresholded images.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Processamento de Imagem Assistida por Computador / Biologia Computacional / Microvasos / Microscopia de Fluorescência Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Processamento de Imagem Assistida por Computador / Biologia Computacional / Microvasos / Microscopia de Fluorescência Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article