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NGS Data Analysis Workshop - Genomic Medicine 2017 Nordic

NGS Workshop 2017 Nordic

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Who should attend?

We welcome all NGS users, researchers and students, as well as bioinformaticians, NHS & Private Labs, Biotech Companies, CRO's, Service providers and anyone else interested in the latest developments of genomics, data analysis, NGS and similar fields to come and join us in this event.

Details

The NGS Data Analysis Workshop 2017 in Sweden is led by Genome Diagnostics Nijmegen. It is held on the 7th November at Lund University, Sweden. The course will be useful for people who are not too experienced in data-analysis but have already some knowledge about NGS. The course will start by providing a good overview of the raw sequencing data, an explanation about the formats and how delegates can check the quality of the data. Following on from this and during the NGS Diagnostics interpretation sections delegates will learn how to work with the analyzed data, how they should interpret the data and how to prioritize the variants to look for the interesting ones. At the conclusion of the course, delegates will be asked to solve diagnostic patient cases by searching for the pathogenic variant(s).

This workshop will be hands-on, so all delegates will need to bring their own laptop.

IMPORTANT: During the workshop the attendees will use real patient data which must be deleted at the end of the workshop.  Your registration to this event provides your agreement that you will abide with this condition and comply appropriately.

Contact

Elisabetta Fineschi
genmednordic@biotexcel.com

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