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Qlucore Insights Lung Cancer model uses molecular data to define subclasses as well as to pinpoint the tissue of origin for lung metastases. Built on AI-based machine learning and transcriptomics the model opens new ways for fast, cost efficient and objective sample analysis. Utilizing standard lab workflows, the program supports analysis of lung tumor and lung disease from fixed and embedded tissue specimens.
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A typical patient presents symptoms like a persistent cough or chest pain, often with a smoking history. Standard workflow begins with a medical history, physical exam, and imaging tests like X-rays and CT scans. Common tests (not extensive list) involve:
Imaging: CT, MRI, PET scans. Biopsies: Needle biopsy, bronchoscopy. Histopathology and molecular tests.
Stages: Ranges from stage 1 (localized) to stage 4 (spread to other parts).
RNA sequencing plays a crucial role in overcoming present challenges in lung cancer diagnostics by measuring two key parameters: chimeric gene fusions and gene expression levels. These measurements help in accurately classifying cancer subtypes and determining the cancer’s origin.
RNA sequencing is set to become widely used in clinical settings by:
• The ability to detect key genetic alterations
• By lowering sequencing costs
• By ease of automation
• Enabling same lab workflow across many different diseases
Many leading laboratories are already offering these analyses.
The Qlucore Insights (RoU) classifier model for lung cancer allows gene expression-based subtype classification of the groups listed below. The cover is broad, with 19 subtypes included. In addition to this, its inbuilt gene fusion analysis supports the identification of druggable as well as novel gene fusions.
Performance in terms of accuracy is described in this POSTER.
View a draft example of how a report might look. Note that the example report is generated with Qlucore Insights (Research Use Only).
This study demonstrates that Qlucore Insights can analyze lung tumors and lung diseases with high accuracy.