Expansion Area 5 proteomics data
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The EA5 pilot was done in collaboration with the Blood Service Biobank, and the samples were collected from blood donors who were heterozygous or homozygous carriers of specific genetic variants of interest. The list of those variants of interest was suggested and approved by the Steering Committee at the beginning of the study and can be found .
The data were generated as part of the FinnGen 2 Expansion Area 5 (EA5) pilot. For the analysis, we used Olink Explore 3072 and SomaScan 7K platforms.
Olink batches 1, 2, and 3
Total number of samples is 1,990 and it contains the data and analysis of the Olink batches 1, 2 and 3.
Batch 1: Rare variant carriers (healthy blood donors)
Batch 2.1: Rare variant carriers (healthy blood donors)
Batch 2.2: Twins (selected from Twingen)
Batch 3: Rare variant carriers (GeneRisk cohort)
The raw data:
Batch 1: finngen/library-red/EA5/proteomics/olink/first_batch/original_data/
Batch 2.1: finngen/library-red/EA5/proteomics/olink/second_batch/
Batch 2.2: To be added
Batch 3: finngen/library-red/EA5/proteomics/olink/third_batch/original_data/
QCed data: finngen/library-red/EA5/proteomics/olink/third_batch/QCd/proteomics_QC_all.txt
pqtl, finemap and auto reporting results are at gs://finngen-production-library-green/omics/proteomics/release_2023_10_11/
Olink batch 1 and 2
Total number of samples is 1,534 and it contains the data and analysis from the batches 1 (n=813) and 2 (n=721).
After QC and ID mapping the number of individuals in the analysis is 1,243.
Raw proteomics data of batch 2 and combined batch 1+2:
finngen/library-red/EA5/proteomics/olink/second_batch/
pQTL and finemapping results:
library-green/omics/proteomics/release_2023_08_08/data/Olink/Finemap/
library-green/omics/proteomics/release_2023_08_08/data/Olink/pQTL/
Colocalization results:
gs://finngen-production-library-green/finngen_R11/finngen_R11_analysis_data/colocalization/data/fg_r11_Olink_batch1_and_2.txt.gz
Raw data:
library-red/EA5/proteomics/soma/second_batch/QCd/SOMA_batch_1_2_QC_all_v2.tx
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pQTL and finemapping results:
library-green/omics/proteomics/release_2023_08_08/data/Somascan/Finemap/
library-green/omics/proteomics/release_2023_08_08/data/Somascan/pQTL/
Colocalization results:
library-green/finngen_R11/finngen_R11_analysis_data/colocalization/data/fg_r11_Soma_v2.txt.gz
Readme:
gs://finngen-production-library-green/omics/proteomics/release_2023_08_08/readme.txt
Explanation of the result columns can be found from
Total number of samples analyzed with SomaScan is 1,000 individuals. These are the same individuals from which data was also generated.
Link to explanation of result file