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Old 06-12-2013, 02:29 PM   #1
Location: SF Bay area

Join Date: Mar 2012
Posts: 20
Default eSeminar June 18th

Join us for an eSeminar June 18th, Introducing the HaloPlex Next Generation Sequencing Panels Targeting Cancer and Inherited Diseases for Research

Learn More:

eSeminar description: The ability to detect sequence level variations through next generation sequencing in a fast, cost effective application has revolutionized the field of genetics. In order to harness the power of next generation sequencing for specific disease states, it is critical to target these specific genomic regions. Developed in conjunction with clinical research industry leaders, Agilent Technologies offers HaloPlex next generation sequencing target enrichment panels for researching specific genetic disorders.

Agilentís 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.

eSeminar presenters: Sheila Purim, Product Manager, Agilent Technologies and Anniek De Witte, Product Manager, CGH and NGS Software, Agilent Technologies, Inc.
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