Genetic Variant Detection in Cancer: Using ISH to Track Tumor Evolution

Intratumor heterogeneity (ITH) is a major underlying cause of therapy resistance and disease recurrence and is a read-out of how a tumor has grown. Current methods to analyze genetic ITH rely on the sequencing of ‘bulk’ or flow-sorted populations, in which the spatial context of tumor subclones is not preserved, and rare subclones may not be detected. These shortfalls can be addressed with BaseScope™ ISH–a unique mutation-specific RNA in situ hybridization assay. The BaseScope assay represents a significant technical advance for in situ mutation detection and provides new insight into the mechanisms of tumor evolution with potential ramifications for selecting patients for treatment. Join us to learn more about this new approach to ITH analysis.
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Spotlight

OTHER ON-DEMAND WEBINARS

Biomarker Driven Drug Development

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Dramatic responses observed with targeted agents in the ‘right’ genomic context have fueled large scale sequencing efforts to identify ‘effective’ treatments for a given patient. In order to expeditiously evaluate a targeted agent against a potential ‘driver’ genetic aberration, so-called Basket trials are conducted.
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Effective Pharmacovigilance Content Collaboration with Cloud Technologies

In an increasingly complex and global pharmacovigilance environment, the need for more effective and easier collaboration is accelerating adoption of cloud technologies.
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Quality Risk Management Commissioning & Qualification: Key Deliverables & Lessons Learned Webinar

It Is Approaching Two Years since Publication of the 2ND Edition Commissioning & Qualification (C&Q) Ispe Baseline Guide.
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Terminal Sterilization or Aseptic Assembly? Consider all options for your Pharma product.

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Regulation is clear that, whenever possible, products intended to be sterile should be terminally sterilized in their final container. Only if terminal sterilization is not possible, filtration or aseptic assembly should be applied. This webinar will focus on elements to evaluate prior to selecting aseptic assembly for the manufacturing of sterile drug products.
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