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Halo 2.3 platform

Manufactured by Indica Labs

The HALO 2.3 platform is a high-performance digital pathology solution developed by Indica Labs. It is designed to enable efficient analysis and management of whole slide images. The HALO 2.3 platform provides advanced image processing and analysis capabilities, facilitating the comprehensive evaluation of tissue samples.

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Lab products found in correlation

2 protocols using halo 2.3 platform

1

Quantifying Mucosal Immune Cells in Tissue

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Images were analyzed using the HALO 2.3 platform (Indica Labs) in a blinded fashion. All tissues were annotated to limit analysis to the mucosa (i.e. epithelium, lamina propria), including lymphoid aggregates and putative colonic patches originating within the submucosa that breached the muscularis mucosa and penetrated into the lamina propria. The submucosa and tunica muscularis were excluded from analysis. For neutrophil quantification, the percentage of MPO positive cells was determined relative to the total cell population using the Cytonuclear v1.6 module. MX1 was quantified as the percent positive staining relative to the total tissue area using the Area Quantification v2.0.0 analysis module. For ILC3 quantification, the number of CD117+CD3, CD117CD3+, and total cells was determined using the FISH v1.1 analysis module. All analyses were reviewed manually to ensure accuracy.
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2

Quantifying Mucosal Immune Cells in Tissue

Check if the same lab product or an alternative is used in the 5 most similar protocols
Images were analyzed using the HALO 2.3 platform (Indica Labs) in a blinded fashion. All tissues were annotated to limit analysis to the mucosa (i.e. epithelium, lamina propria), including lymphoid aggregates and putative colonic patches originating within the submucosa that breached the muscularis mucosa and penetrated into the lamina propria. The submucosa and tunica muscularis were excluded from analysis. For neutrophil quantification, the percentage of MPO positive cells was determined relative to the total cell population using the Cytonuclear v1.6 module. MX1 was quantified as the percent positive staining relative to the total tissue area using the Area Quantification v2.0.0 analysis module. For ILC3 quantification, the number of CD117+CD3, CD117CD3+, and total cells was determined using the FISH v1.1 analysis module. All analyses were reviewed manually to ensure accuracy.
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