Sunday, April 22, 2012

Sneak Peak: A Practical Approach to Detecting Nucleotide Variants in NGS Data

Join us Thursday, May 3, 2012 9:00 am (Pacific Time) for a webinar on analyzing DNA sequencing data with hundreds of thousands to millions of nucleotide variants.

This webinar discusses DNA variant detection using Next Generation Sequencing for targeted and exome resequencing applications as well as, whole transcriptome sequencing. The presentation includes an overview of each application and its specific data analysis needs and challenges with a particular emphasis on variant detection methods and approaches for individual samples as well as multi-sample comparisons. For in depth comparisons of variant detection methods, Geospiza’s cloud-based GeneSifter® Analysis Edition software will be used to assess sample data from NCBI’s GEO and SRA.

For more information, please visit the registration page.