Webinar "Better care with better knowledge"

Vabimo vas, da se pridružite webinarju našega principala, podjetja Qiagen, o interpretaciji kliničnih podatkov sekvenciranja naslednje generacije (NGS) in zmanjšanju števila manj pomembnih variant, ki bo 26.3.2018, od 19h do 20h.

As more patient samples are sequenced around the world, we are on the verge of understanding the genetic basis of disease. After 20 years of manually curating genetic evidence and partnering with clinical testing labs, QIAGEN is now a leader in aggregating the world’s knowledge of genetic diseases. With the experience of having interpreted over 500,000 human samples, QIAGEN’s knowledge base is the most comprehensive in the world. 

Join us for a webinar to learn how this integrated knowledge base can provide you with clinical evidence for rapid interpretation of next-generation sequencing (NGS) data, as well as reduce the number of variants of unknown significance in NGS interpretation.  
 
Speaker: Rupert Yip, PhD Assoc. Director, Genetic Disease Informatics – QIAGEN

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