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Qlucore Omics Explorer video
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Our CE-marked IVDR tool, Qlucore Diagnostics, revolutionizes RNA-seq cancer diagnostics for Acute Lymphoblastic Leukemia (BCP-ALL). It offers precise gene expression subtype classification of B-cell leukemias and gene fusion analysis support.
We’re continuously working to expand our certification to include additional cancer types, ensuring broader diagnostic capabilities and improved patient outcomes.
Qlucore Diagnostics offers a scalable, end-to-end (data to report) diagnostic solution, transforming data into actionable reports. Our platform combines machine learning-based subtype classification with intuitive reporting and visualization, ensuring clear communication between labs, clinicians, and patients.
The Qlucore Diagnostics Platform is designed for use with one or several Qlucore Diagnostics Models, intended for trained healthcare professionals in clinical laboratory settings. Key roles include geneticists, laboratory scientists, bioinformaticians, and medical specialists in genetics and oncology for interpreting the report.
The workflow from patient sample to the output from Qlucore Diagnostics is outlined in the figure below:
Our Qlucore Diagnostics BCP-ALL software is an in-vitro diagnostic medical device for precision cancer diagnostics based on RNA-seq data. It is designed for installation in hospitals and central clinical labs to analyze, interpret, and display results from next-generation sequencing (NGS) of bone marrow or peripheral blood samples.
Qlucore Diagnostics BCP-ALL assists in classifying samples into subtypes using molecular information. It imports RNA-sequencing data as well as RNA-seq data that have been processed by gene fusion detection algorithms, offering two key features:
Gene fusions are automatically quality-checked and presented in tiers based on their relevance to BCP-ALL. The gene expression analysis supports subtype classification, enhancing diagnostic accuracy.
View a draft example of how a report might look.