Copy number variations and their effect on the plasma proteome | Associations

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).