Published September 15, 2022
| Version v1
Dataset
Restricted
Characterizing Copy Number Variations and their association with plasma proteins using short and long-read sequencing | Association Results
Authors/Creators
- 1. Department of Immunology, Genetics and Pathology, Science for Life Laboratory, Uppsala University
- 2. Twelve Bio ApS, Copenhagen, Denmark
- 3. Department of Medical Biochemistry and Microbiology, National Bioinformatics Infrastructure Sweden, Science for Life Laboratory, Uppsala University, Uppsala, Sweden
Description
Results from a GWAS investigation the relationship of CNVs and blood protein measurements.
Notes
The NSPHS was funded by the Foundation for Strategic Research (UG) and the European Commission FP6 (UG). Sequencing was performed by NGI (National Genomics Infrastructure), Sweden. Protein measurements were carried out by Olink Proteomics AB in Uppsala, Sweden. The computations and data handling were enabled by resources in project sens2016007 provided by the Swedish National Infrastructure for Computing (SNIC) at Uppsala Multidisciplinary Centre for Advanced Computational Science (UPPMAX), partially funded by the Swedish Research Council through grant agreement no. 2018-05973. Short read sequencing was funded by the Science for Life Laboratory (SciLifeLab) and Swedish Genomes Program, which has been made available by support from the Knut and Alice Wallenberg Foundation. Long-read sequencing was supported by the Marcus Borgström's and Hedström's foundations. This work was also funded by the Swedish Medical Research Council (2019-01497) and the Swedish Heart-Lung foundation (nr. 20200687).
Files
Restricted
The record is publicly accessible, but files are restricted. Log in to check if you have access.