ID
45885
Descrizione
Principal Investigator: Stacey Gabriel, PhD, Broad Institute, Boston, MA, USA MeSH: Myocardial Infarction https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000990 MI cases were recruited from the German MI Family Study and the Angio-Lub study. Controls were recruited from the German MI Family Study and the Angio-Lub study. All exome sequencing was performed at the Broad Institute of Harvard and MIT; samples sequence capture was performed using Illumina's ICE Capture reagent and sequencing was performed on an Illumina HiSeq 2000 or 2500.
collegamento
Keywords
versioni (1)
- 18/11/23 18/11/23 - Simon Heim
Titolare del copyright
Stacey Gabriel, PhD, Broad Institute, Boston, MA, USA
Caricato su
18 novembre 2023
DOI
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Licenza
Creative Commons BY 4.0
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dbGaP phs000990 MIGen_ExS: University of Lubeck
This subject consent file contains subject IDs, consent group information, and affection status for myocardial infarction.
- StudyEvent: SEV1
- This subject consent file contains subject IDs, consent group information, and affection status for myocardial infarction.
- This subject sample mapping file contains 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. The data table also includes sample use.
- This subject phenotype data table contains gender of participants.
- This sample attributes data table includes sample analyte type.
Similar models
This subject consent file contains subject IDs, consent group information, and affection status for myocardial infarction.
- StudyEvent: SEV1
- This subject consent file contains subject IDs, consent group information, and affection status for myocardial infarction.
- This subject sample mapping file contains 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. The data table also includes sample use.
- This subject phenotype data table contains gender of participants.
- This sample attributes data table includes sample analyte type.