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About the project

about_the_project_smallThe landscape of genetic testing is rapidly changing. Soon, whole genome sequence analysis (3Gb-testing) will be an effective and financially viable alternative to targeted gene analysis.
New technologies that allow efficient sequencing of a whole human genome in a diagnostic setting will have an enormous impact on diagnostic centres replacing many existing molecular and cytogenetic tests.
Patients deserve to benefit from our vastly growing knowledge on functional genomics. 3Gb-testing is the ideal method to bring these benefits to the public.

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México

9th -13th October 2017: Translational Genomics and NGS in a diagnostic setting

October 9th: Symposium on Translational Genomics “Genomics and Health”

October 10th – 13th: 3Gb-TEST NGS Course in a diagnostic setting

The focus of the course is on clinical diagnostics using exome/genome sequences, variant identification and analysis including afternoon practical sessions in dry lab as well as in wetlab. *Event mostly in Spanish


Ljubljana

25th -27th September 2017: 3-day course on NGS Ljubljana, Slovenia

 

A 3-day course on NGS Ljubljana, Slovenia in the period of 25-27 October 2017. The focus of the course is on clinical diagnostics using exome/genome sequences, variant identification and analysis including afternoon practical sessions. For more detailed program please click here.
Registration is open till 20th August. REGISTER Now!