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1.
BMC Bioinformatics ; 22(1): 260, 2021 May 22.
Artículo en Inglés | MEDLINE | ID: mdl-34022787

RESUMEN

BACKGROUND: Recent advances in tissue clearing techniques, combined with high-speed image acquisition through light sheet microscopy, enable rapid three-dimensional (3D) imaging of biological specimens, such as whole mouse brains, in a matter of hours. Quantitative analysis of such 3D images can help us understand how changes in brain structure lead to differences in behavior or cognition, but distinguishing densely packed features of interest, such as nuclei, from background can be challenging. Recent deep learning-based nuclear segmentation algorithms show great promise for automated segmentation, but require large numbers of accurate manually labeled nuclei as training data. RESULTS: We present Segmentor, an open-source tool for reliable, efficient, and user-friendly manual annotation and refinement of objects (e.g., nuclei) within 3D light sheet microscopy images. Segmentor employs a hybrid 2D-3D approach for visualizing and segmenting objects and contains features for automatic region splitting, designed specifically for streamlining the process of 3D segmentation of nuclei. We show that editing simultaneously in 2D and 3D using Segmentor significantly decreases time spent on manual annotations without affecting accuracy as compared to editing the same set of images with only 2D capabilities. CONCLUSIONS: Segmentor is a tool for increased efficiency of manual annotation and refinement of 3D objects that can be used to train deep learning segmentation algorithms, and is available at https://www.nucleininja.org/ and https://github.com/RENCI/Segmentor .


Asunto(s)
Procesamiento de Imagen Asistido por Computador , Microscopía , Algoritmos , Animales , Encéfalo , Imagenología Tridimensional , Ratones
2.
Cell Rep ; 37(2): 109802, 2021 10 12.
Artículo en Inglés | MEDLINE | ID: mdl-34644582

RESUMEN

Tissue-clearing methods allow every cell in the mouse brain to be imaged without physical sectioning. However, the computational tools currently available for cell quantification in cleared tissue images have been limited to counting sparse cell populations in stereotypical mice. Here, we introduce NuMorph, a group of analysis tools to quantify all nuclei and nuclear markers within the mouse cortex after clearing and imaging by light-sheet microscopy. We apply NuMorph to investigate two distinct mouse models: a Topoisomerase 1 (Top1) model with severe neurodegenerative deficits and a Neurofibromin 1 (Nf1) model with a more subtle brain overgrowth phenotype. In each case, we identify differential effects of gene deletion on individual cell-type counts and distribution across cortical regions that manifest as alterations of gross brain morphology. These results underline the value of whole-brain imaging approaches, and the tools are widely applicable for studying brain structure phenotypes at cellular resolution.


Asunto(s)
Núcleo Celular/patología , Corteza Cerebral/patología , Técnicas de Preparación Histocitológica , Degeneración Nerviosa , Neuroglía/patología , Neuroimagen , Neuronas/patología , Animales , Núcleo Celular/metabolismo , Corteza Cerebral/metabolismo , ADN-Topoisomerasas de Tipo I/deficiencia , ADN-Topoisomerasas de Tipo I/genética , Eliminación de Gen , Genes de Neurofibromatosis 1 , Procesamiento de Imagen Asistido por Computador , Ratones Noqueados , Neuroglía/metabolismo , Neuronas/metabolismo , Fenotipo , Máquina de Vectores de Soporte
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