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Scn file format

Manufactured by Leica

The SCN file format is a proprietary file format developed by Leica Microsystems for storing and managing image data acquired through their microscope systems. It is designed to capture and preserve the high-quality digital images generated by Leica's advanced imaging equipment.

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2 protocols using scn file format

1

Digital Pathology of Papillary Urothelial Carcinoma

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The data material consists of digital whole-slide images from patients diagnosed with primary papillary urothelial carcinoma, collected at the University Hospital of Stavanger, Norway, in the period 2002-2011. The biopsies are formalin-fixed and paraffin-embedded, from which 4 μm slices are cut and stained with Hematoxylin Eosin Saffron (HES).
The prepared tissue samples are scanned at 400x magnification using the Leica SCN400 slide scanner, producing image files in Leica’s SCN file format. The images are stored as a pyramidal tiled image with several down-sampled versions of the base image in the same file to accommodate for rapid zooming. Each level in the file is down-sampled by a factor of 4 from the previous level. Figure 2 shows an example of a pyramidal histological image with three levels. The Vips library27 is capable of extracting the base image as well as the down-sampled versions, making it easy to extract the dataset at each resolution.
Two datasets were collected from the described data material, referred to as the CV dataset and the inference dataset, both are described below.
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2

Quantitative Analysis of IHC and ISH Images

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IHC- and ISH-stained slides were imaged using brightfield whole-tissue scanning by an Aperio Versa 8 (Leica Biosystems) at 20x/0.80NA, 40x/0.85NA, and oil 63x/1.30NA objectives. Digitized images (Leica .SCN File Format) were viewed and annotated using Aperio eSlide Manager. Monochrome images for FISH and IFA-stained slides were captured for each fluorophore using an Olympus DP80. A pseudo color was applied using the CI Deconvolution algorithm (Olympus) for each marker and fused into a composite image for viewing. Image processing and analysis for IHC- and ISH-stained slides were performed using the Area Quantification and Deconvolution modules of Halo Image Analysis Platform (Indica Labs, Inc). Using the deconvolution module, brightfield images were converted to pseudo fluorescent images for representation purposes only. This was done by applying contrasting color pairs for portions of the tissue that matched the optical density values for Hematoxylin and DAB/Warp Red staining. Using the Area Quantification module, the percentage of tissue area positive for Warp Red ISH staining was generated using the optical density for Warp Red chromogen and Hematoxylin as a portion of the entire tissue area analyzed.
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