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Scanscope cs microscope slide scanner

Manufactured by Leica
Sourced in Germany

The ScanScope CS microscope slide scanner is a high-performance digital imaging system designed for the efficient digitization of microscope slides. The core function of this product is to capture high-quality digital images of microscope specimens, enabling researchers and clinicians to view and analyze samples remotely or in a digital format.

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2 protocols using scanscope cs microscope slide scanner

1

Quantitative Histological Image Analysis

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The ScanScope CS microscope slide scanner (Leica Biosystems) was used to digitize whole slide images of histological sections at 20 × (0.5 µm/pixel) and record them as tiled tiff images.
For each image, regions of interest (ROIs) were drawn using the ImageScope software (Leica Biosystems) in order to select only tumor tissues and remove the artifacts. The images were processed as reported in the previous study (25 (link)). Briefly, squares of 2000 pixels size corresponding to 1 mm2 area were used in this study. The squares were generated to fit the area of the ROI. A ratio between the stained area (brown color) and the surface of tissue was computed and assigned to each square based on their coordinates. Local ratio computed for each square was ranked according to the following ten intervals: level 0 (0–10%), level 1 (>10–20%), level 2 (>20–30%), level 3 (>30–40%), level 4 (>40–50%), level 5 (>50–60%), level 6 (>60–70%), level 7 (>70–80%), level 8 (>80–90%), and level 9 (>90–100%). The ranks then formed the basis for the co-occurrence matrix used to compute Haralick texture parameters. The classical Haralick parameters (26 (link)) were computed from the normalized co-occurrence matrix: contrast, homogeneity, dissimilarity, entropy, energy, and correlation. The descriptors of the distribution shape were also computed: skewness and kurtosis.
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2

Quantifying Cardiac Collagen Deposition

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Mice were euthanized by cervical dislocation under isoflurane anesthesia, and the hearts were excised and sectioned into two parts (basal and apical). Sections were fixed and embedded in paraffin. A 6 μm-section of each part was sliced and stained with Picro-Sirius Red (Ral-diagnostics, Bordeaux, France) to reveal collagen I and III fibers. Whole-slide images of histological sections were digitized at 20× using a ScanScope CS microscope slide scanner (Leica Biosystems, Nussloch, Germany). ImageScope software (Leica Biosystems, Nussloch, Germany) was used to draw global regions of interest (ROIs) for each slice. ROIs were processed to determine the amount of collagen using the programming language Python (Python Software Foundation) and the libraries Openslide, Geospatial Data Abstraction and Mahotas [16 (link)]. The amount of collagen in the basal and apical slices was averaged for analysis.
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