Next-Generation Sequencing Videos

SureSelect and HaloPlex - Two technologies, one complete solution

Agilent offers a fully validated protocol for integrated genomic DNA sample prep, library construction, and target enrichment, covering the entire Next-Generation Sequencing Workflow. Learn more in these informative eSeminars.

For Research Use Only. Not for Use in Diagnostic Procedures.

 

   
Optimizing Whole-Transciptome RNA-Seq with Improved Library Prep and Data Analysis  

Optimizing Whole-Transciptome RNA-Seq with Improved Library Prep and Data Analysis

Dr. Ravi Madduri, M.S. Navipoint Genomics and University of Chicago, and Alex Siebold, Agilent Technologies. This online seminar outlines how improvements on the front end and back end of the sequencing workflow can lead to better RNA-seq results from FFPE samples.

High-Confidence Mutation Detection in Chronic Lymphocytic Leukemia Gene Targets  

High-Confidence Mutation Detection in Chronic Lymphocytic Leukemia Gene Targets

Rajesh Singh, MD Anderson Cancer Center. Dr. Singh discusses how his team applied the HaloPlexHS workflow to variant detection in CLL gene targets.

ONCOgenics: A novel NGS platform for somatic and germline oncology  

ONCOgenics: A novel NGS platform for somatic and germline oncology

Juan Cadinanos, Ph.D., Director of the Laboratory of Molecular Medicine at IMOMA
ESHG Conference, Barcelona, May 23, 2016
The design and development of NGS panels for somatic and germline cancer analysis using Agilent custom SureSelect Target Enrichment.

Lowering the stakes to raise the bar: Building an NGS panel to meet the needs of today  

Lowering the stakes to raise the bar: Building an NGS panel to meet the needs of today

Jennifer Morrissette, Ph.D., Karthik Ganapathy, Ashkan Bigdeli, University of Pennsylvania. Design and analytical validation of an NGS panel for solid tumor analysis using HaloPlex technology.