GENOMIC MEDICINE NORDIC WORKSHOP 2018 - Genomic Medicine 2018 Nordic Workshop

Website https://biotexcel.com/event/genomic-medicine-2018-nordic/ | Edit Freely

Category Genomics, Genetics, NGS, Next Generation Sequencing, bioinformatics, clinical genetics, oncology, cancer, clinical genomics, molecular biology, data analysis, human genetics, biomarkers, data storage, rare disease, micro RNA, circulating tumour DNA, cfDNA, miRNA, Epigenetics, Transcriptomics, Oncogenomics, microbiome, metagenomics, NGS Data Analysis, Personalized Medicine, Diagnostics

Deadline: October 01, 2018 | Date: October 01, 2018

Venue/Country: Campusvej 55, 5230 Odense, Denmark

Updated: 2018-02-22 00:44:13 (GMT+9)

Call For Papers - CFP

The 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.

The bioinformatics team will consist of the following teachers;

Marin Larsen, ass. Prof., PhD, molecular biologist, bioinformatician at OUH in charge of the clinical sequencing data acquisition.

Mark Burton, ass. Prof., PhD, molecular biologist, bioinformatician handling quantitative sequencing data and statistics

Lars Andersen, PhD-student, mathematician, handling various models requiring advanced computation.

Klaus Brusgaard, assoc Prof., PhD, molecular biologist, evaluating genetic variants using various databases and prediction tools.