SNIC SUPR
Genomic aggregation project of Sweden - GAPS
Dnr:

sens2017599

Type:

SNIC SENS

Principal Investigator:

Patrick Sullivan

Affiliation:

Karolinska Institutet

Start Date:

2018-01-10

End Date:

2021-02-01

Primary Classification:

30107: Medical Genetics

Webpage:

Allocation

Abstract

There are current project data which are part of the project b2015249 on Milou. Those data need to be transferred to Bianca. The overall goal of GAPS is to aggregate existing genomic data from appropriately consented Swedish subjects, and perform joint analyses, to increase the understanding of the basis of biomedical disorders with large impacts on the public health of Sweden. One of the specific aims are to contribute to a Swedish national variant frequency database, and to understand the genetic basis of several critically important psychiatric disorders (schizophrenia, major depressive disorder, autism, bipolar disorder, and eating disorders), and their association with educational attainment.