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Genomics and future healthcare

Conference November 26th, 2014 in Copenhagen

CONFERENCE PROGRAM (download PDF version)

Session

Time

Title

Speaker

1

09.00

Introduction to the conference
          and GenomeDenmark platform

Esben Flindt

09.05

A national Danish Genomics Initiative

Thomas Bjørnholm

09.15

The Danish Pangenome 

Karsten Kristiansen

09.25

Tracing pathogens in cancer

Eske Willerslev

09.35

Whole-genome sequencing: Technologies and benefits

Radoje Drmanac

10.05

Finding viruses using deep sequencing
          - discovery to proof of disease association

Paul Kellam

10.35

Break

2

11.00

Large scale sequencing and clinical microbiology

Tobias Allander

11.30

Personal genomes

Jun Wang

12.00

Genome sequencing and clinical genetics for patients

Joris Veltman

12.30

Break

3

13.30

Molecular strategies for pathogen discovery
          in cancer samples

Sarah Mollerup

13.40

Identification of viral cancer drivers:
          Combined use of NGS and Bioinformatics

José Izarzugaza

13.50

Building the Danish Pan-genome

Simon Rasmussen

14.00

The rate of indels and point mutations in the
          human germline

Søren Besenbacher

14.10

Coupling genomics and register data for identification
          of etiologies in mental disorders

Anders Børglum

14.20

Mining and linking data from genomics and patient journals

Søren Brunak

14.30

Bridging between registry data and biobank materials

Mads Melbye

14.40

Genomic Medicine

Finn Cilius

14.50

Challenges in using genomics in personalized health care

Thorkild Sørensen

15.00

Break

4

15.25

Challenges for public health prevention and care

Else Smith

15.45

Ethical issues in whole-genome sequencing research

Lene Koch

16.00

Panel discussion

Panel

16.50

Perspectives and rounding off

K. Kristiansen & A.J. Hansen

17.00

Conference finishes