ID
45969
Beschreibung
Principal Investigator: Stacey Gabriel, PhD, Broad Institute, Boston, MA, USA MeSH: Coronary Artery Disease https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000883 The Precocious Coronary Artery Disease (PROCARDIS) study is an international, multicenter case-control study aimed at discovering the genetic contributors to premature coronary artery disease. All exome sequencing was performed at the Broad Institute of Harvard and MIT; samples sequence capture was performed using Agilent SureSelect Human All Exon Kit v2 and sequencing was performed on an Illumina HiSeq 2000 or 2500.
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- 26.03.24 26.03.24 - Madita Rudolph
Rechteinhaber
Stacey Gabriel, PhD, Broad Institute, Boston, MA, USA
Hochgeladen am
26. März 2024
DOI
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Creative Commons BY 4.0
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dbGaP phs000883 MIGen_ExS: PROCARDIS
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- This subject consent file contains subject IDs, consent group information, and affection status. Cases were considered eligible for the study if premature coronary artery disease was present. Controls were matched by age and gender and recruited from the same centers simultaneously.
- 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.
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Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- This subject consent file contains subject IDs, consent group information, and affection status. Cases were considered eligible for the study if premature coronary artery disease was present. Controls were matched by age and gender and recruited from the same centers simultaneously.
- 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.
C0680251 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,2])
C1706256 (UMLS CUI [1,3])
C1867743 (UMLS CUI [1,4])
C0009932 (UMLS CUI [2,1])
C1708943 (UMLS CUI [2,2])
C0079399 (UMLS CUI [2,3])
C0001779 (UMLS CUI [2,4])
C1867743 (UMLS CUI [2,5])
C0549184 (UMLS CUI [2,6])