This is the third Edition of the Three Day Course on Variant Detection and Interpretation in a Diagnostic Context.
20 – 22 September 2016
VKGL/VKGN ‘NGS in DNA diagnostics’ is a course aimed at Genomic Resequencing in a Medical Diagnostic Context, i.e. to apply Next Generation Sequencing data as diagnostic tool in the hospital. Lectures will be accompanied with hands-on exploration.
- Day 1 consists of an introduction to NGS techniques followed by specialized lectures on sample preparation, enrichment technologies and read mapping.
- Day 2 will continue with lectures on variant calling, annotation and interpretation with a diagnostic emphasis applied to Gene Capturing Panels, Exome Screening and CNV analysis.
- The afternoon of Day 1 & Day 2 is reserved for workshops and software demonstrations. Real data will be used where possible in hands-on tutorials using both commercial and open source software.
- Day 3 focuses on impact of results in the lab and ethical and legal issues of NGS in the clinical application. Real-life applications of NGS in the clinic will be presented. A forum discussion between researchers and clinicians about mutual expectations, ethics, implications of NGS on diagnostics and data sharing concludes the day.
This course is intended for bioinformaticians, researchers and molecular & clinical geneticists. The mixed programme will appeal to all those requiring a solid background in the application of NGS techniques for (routine) genetic diagnosis of a patient. The course will be mainly in English.
Organisation, Accreditation and Registration
The course is a joint effort from individuals of the NVHG/VKGL/VKGN (diagnostic) community of The Netherlands. Accreditation is be filed for at VKGL and VKGN (6 points; GAIA registration is pending).
Organisers: Jasper Saris, Christian Gilissen, Rob van der Luijt, Johan den Dunnen
Contact person: Mrs. S. Ghiraw, email@example.com
Course website: link to course website
This course including self-study is 1,0 ECTS.