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 New data release
Want to improve your bioinformatics skills? Book a seat at our NGS analysis workshops in October or at the promoter analysis seminar in September! Genomatix has released a new version of the BLUEPRINT visual interface allowing users to visualize epigenetic data from the BLUEPRINT project. A new data release of the Genomatix Software Suite is now available. New data include the human GRCh38 reference genome, additional GenomeBrowser tracks, ...
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