ID
45704
Beschreibung
Principal Investigator: Eric Lander, The Broad Institute of Harvard and MIT, Cambridge, MA, USA MeSH: Population Groups https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001230 The Estonian Biobank is the population-based biobank of the Estonian Genome Centre of University of Tartu. The biobank is conducted according to the Estonian Gene Research Act and all participants have signed broad informed consent. The cohort size is currently 51,535 people from 18 years of age and up. Metabolite concentrations (over 110; NMR and MS) are available for about 12,000 subjects; metabolic follow-up has been done for more than 2000 donors. GWAS has been performed on 20,000 subjects with different Illumina arrays and 2,500 have whole exomes and 2,400 full sequence. The data for the 2,400 fully sequenced samples is available through dbGaP.
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- 16.05.23 16.05.23 - Chiara Middel
Rechteinhaber
Eric Lander, The Broad Institute of Harvard and MIT, Cambridge, MA, USA
Hochgeladen am
16. Mai 2023
DOI
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Lizenz
Creative Commons BY 4.0
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dbGaP phs001230 Estonian Biobank | Estonian Genome Center, University of Tartu
The subject consent data table contains subject IDs and consent group information.
- StudyEvent: SEV1
- The subject consent data table contains subject IDs and consent group information.
- This subject sample mapping data table includes a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs.
- This subject phenotype table includes subject's sex.
- This sample attributes table includes analyte type.
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The subject consent data table contains subject IDs and consent group information.
- StudyEvent: SEV1
- The subject consent data table contains subject IDs and consent group information.
- This subject sample mapping data table includes a mapping of study subject IDs to sample IDs. Samples are the final preps submitted for genotyping, sequencing, and/or expression data. For example, if one patient (subject ID) gave one sample, and that sample was processed differently to generate 2 sequencing runs, there would be two rows, both using the same subject ID, but having 2 unique sample IDs.
- This subject phenotype table includes subject's sex.
- This sample attributes table includes analyte type.