Program

13:00 - 13:05

Welcoming remarks

14:25 - 14:45

Valtteri Wirta, Clinical Genomics Facility, SciLifeLab.

13:05 - 13:35

Introduction to NGI and Whole Genome Sequencing services.

13:35 - 14:05

Keynote speaker: Initiatives based on genomes and e-health databases in Estonia

Lili Milani, University of Tartu

14:05 - 14:25

A geographically and phenotypically matched control population enables unbiased whole-genome analysis

for variants causing autosomal dominant diseases

Erik Johansson, UmU.

15:35 - 15:55

SweGen: A Swedish 1000 genomes project.

Adam Ameur, UU/NGI

15:15 - 15:35

Genomic profiling of pediatric brain tumors within The Swedish Childhood Tumor Biobank

Teresita Diaz de Ståhl, KTH

14:45 - 15:15

Coffee break, poster session, mingle

15:55 - 16:15

Genomic Medicine Sweden initiative

Richard Rosenquist Brandell, KI

16:15 - ...

Poster session, consultations, mingle.

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