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Epredia™ 3DHistech SlideManager Workflow Management Software/20 Users, QuantServer Server-Side Analysis Application/9 Users
Epredia™ 3DHistech SlideManager and QuantServer is a software package for integrated workflow management designed to support the researcher's work from defining the project through the collection and organization of samples to analysis and export.
Supplier: Epredia™ 94433
Description
SlideManager is an integrated workflow management software designed for research purposes, which supports the researcher's work from defining the project through the collection and organization of samples to analysis and export.
Key features of SlideManager:
- Integrated and intuitive web-based user interface on which the entire workflow can be followed and managed.
- The system enables the management of users and user roles, as well as the collaborative use of projects.
- The system thinks in terms of research projects, which is a set of slides that can be hierarchized into groups. Metadata relevant to the research can be recorded for both the projects and the slides.
- Integration with SlideCenter: from which users can import slides for the project.
- The system enables the normalization of slides prepared and stained in different ways, after which the slides can be evaluated quantitatively due to the same coloring.
- Integration with QuantServer: starting the normalization, region selection, image processing, evaluation, and display of data.
- Integration with SlideViewer:
- Integration SimpleSlideInterface: which allows researchers and external image processing software to access slides, folders, images, annotations, from any scripting or programming environment (e.g., Python script).
- Backup and Restore features
- License for 20 users.
- QuantServer module allows you to execute processing and store the analyzation results on a dedicated server.
- License for 9 users - Research use only.
Specifications
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For research and education use only, not for use in diagnostic procedures in the U.S. This product has not been approved or cleared as a medical device by the U.S. Food and Drug Administration.