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Streamlined solutions for somatic and germline disease variant interpretation and reporting - QIAGEN Digital Insight User Group Meeting Online Summit
The entire way from FASTQ to report... Fast!

Join us for a two-day online summit – featuring product updates and training in our bioinformatic solutions, as well as Q&A sessions with experts. Our goal is to help users learn from each other, our experts, and industry leaders. We aim to gather your valuable input for product development and to build long-term relationships.

October 7, 2020 - Day 1 – Somatic cancer
October 8, 2020 - Day 2 – Hereditary cancer and germline disorders

Agenda (CEST): https://tinyurl.com/y5b5h55x
Agenda (EDT): https://tinyurl.com/y2nuq9z4

Somatic cancer
If your work involves NGS variant interpretation, CNVs, TMB, or MSI, and you need to recommend treatment based on the current guidelines (such as ESMO, AMP, EMA, etc.) and up-to-date scientific literature, we encourage you to join October 7.

Hereditary cancer and germline disorders
If your work involves hereditary cancer or disease, large panels, WES (including trios), WGS, carrier screening, or you want to learn how to prioritize variants based on observed phenotypes, we encourage you to join on October 8.

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You can choose to attend one or more of the following webinars.


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