CLINICAL NGS DATA ANALYSIS WORKSHOP, 12th November 2019 at Kennedy Center (Copenhagen)
This workshop will aim to go over the steps from acquisition of sequencing data to the generation of the bam- and vcf- files that will be used in the subsequent filtering for variants.
Variants will be evaluated using various databases and prediction tools to establish potential pathogenic variants.
Workshop delegates will be given tutorials and examples and will be expected to handle the data themselves on their own laptops under the teacher's guidance.
The teachers of this workshop will be from the Bioinformatics team of Odense University Hospital (OUH) led by Prof Klaus Brusgaard.
This workshop is part of the Genomic Medicine 2019 Nordic conference. Please contact us if you would like to book the workshop only.
This workshop will aim to go over the steps from acquisition of sequencing data to the generation of the bam- and vcf- files that will be used in the subsequent filtering for variants.
Variants will be evaluated using various databases and prediction tools to establish potential pathogenic variants.
Workshop delegates will be given tutorials and examples and will be expected to handle the data themselves on their own laptops under the teacher's guidance.
The teachers of this workshop will be from the Bioinformatics team of Odense University Hospital (OUH) led by Prof Klaus Brusgaard.
This workshop is part of the Genomic Medicine 2019 Nordic conference. Please contact us if you would like to book the workshop only.
