NGS and personalized medicine: The role of data interpretation

The advance of Next Generation Sequencing (NGS) technology has enabled researchers to generate genome wide data in unprecedented quality and quantity. Genomatix offers solutions and services for the entire course of analysis from first level mapping to integrating multiple results with copious high-quality data background. Our technologies for visualization and interpretation enable scientists world-wide to turn their data into meaningful results, making NGS the perfect vehicle to enable personalized medicine

seminar image BLUEPRINT logo Genomatix at ASHG2014
Learn how to perform NGS data analysis for ChIP-Seq or expression studies in our seminar on November 26/27 2014. You can bring your own data for analysis. Genomatix has released a new version of the BLUEPRINT visual interface allowing users to visualize epigenetic data from the BLUEPRINT project. Genomatix will be at the ASHG2014 in San Diego on October 19-21, 2014. Meet us at booth #1216 to learn more about our solutions and services!
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