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Upcoming eSeminar
Genomic Research Panels Overview and Demo: How to Customize the HaloPlex Cancer Research Panel
Register Today
Agilent has recently launched the HaloPlex Cancer Research panel which enables fast, simple, and efficient analysis of genomic regions of interest for cancer research in a large number of samples. The panel covers COSMIC hotspot mutations in 47 genes. With discoveries in cancer research being made daily, new mutations of known significance are constantly being identified. With ever growing discovery there may be a need to add additional content to a panel.
In this webinar we will walk through how to customize the HaloPlex Cancer Research panel to add additional content. Customization is easily done with SureDesign, the next generation design tool for NGS target enrichment. We will also cover the expanding library of panels for clinical research.
Agilent’s integrated solution for clinical genomics research also includes SureCall, an easy-to-use desktop application that combines best in class open source algorithms for end-to-end NGS data analysis from alignment to categorization of mutations. With this complete workflow, customers can rapidly deploy studies for clinical research.
Learn More
Genomic Research Panels Overview and Demo: How to Customize the HaloPlex Cancer Research Panel
Register Today
Agilent has recently launched the HaloPlex Cancer Research panel which enables fast, simple, and efficient analysis of genomic regions of interest for cancer research in a large number of samples. The panel covers COSMIC hotspot mutations in 47 genes. With discoveries in cancer research being made daily, new mutations of known significance are constantly being identified. With ever growing discovery there may be a need to add additional content to a panel.
In this webinar we will walk through how to customize the HaloPlex Cancer Research panel to add additional content. Customization is easily done with SureDesign, the next generation design tool for NGS target enrichment. We will also cover the expanding library of panels for clinical research.
Agilent’s integrated solution for clinical genomics research also includes SureCall, an easy-to-use desktop application that combines best in class open source algorithms for end-to-end NGS data analysis from alignment to categorization of mutations. With this complete workflow, customers can rapidly deploy studies for clinical research.
Learn More