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Eligibility Criteria

6 forms  
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. The subject consent data table contains subject IDs and consent information.
    3. This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, subjects's sex, twin IDs, and indicator for monozygotic and dizygotic twins.
    4. This data table contains 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.
    5. This subject phenotype table includes subject's sex, age at enrollment, race (n=3 variables; self-reported, race/ethnicity grouped by researcher, and genetically similar population groups), heart diagnoses (n=5 variables; primary diagnoses and classification, other diagnoses, comments, and disease ontology), IPSCORE IDs, and indicators if subject was part of a study/paper (n=10 variables; iPSCORE resource, aberrant iPSC methylation in twins, WGS, eQTL, allele-specific NKX2-5 binding in iPSC-CMs, Hi-C in iPSCs and iPSC-CMs, mutational burden of iPSCs, iPSC-derived retinal pigment epithelium, structural variation in IPSCORE, and lncrnas in iPSC-CMs).
    6. This sample attributes table includes sample histological type, tumor status, analyte type, sample source, other IDs (UCSD source tissue, UCSD iPSC clone, WiCell), sequencing center, clone and passage.
Inclusion and exclusion criteria
Description

Inclusion and exclusion criteria

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0680251
The iPSCORE study had three recruiting approaches: 1) We targeted the recruitment of twins (monozygotic and dizygotic) and their immediate families from a southern California twin registry; 2) We worked with physicians to refer subjects (and their family members) into the study based on a diagnosed cardiovascular disease. In all cases where a physician referred an individual, the clinical diagnosis is provided; 3) Through advertisement on the internet and via fliers, we targeted the recruitment of large families, independent of the presence of twins or individuals with cardiovascular disease.
Description

Elig.phs001325.v3.p1.1

Data type

boolean

Alias
UMLS CUI [1,1]
C0242800
UMLS CUI [2,1]
C0242800
UMLS CUI [2,2]
C0041427
UMLS CUI [2,3]
C0015576
UMLS CUI [2,4]
C0034975
UMLS CUI [3,1]
C0031831
UMLS CUI [3,2]
C0205543
UMLS CUI [3,3]
C0011900
UMLS CUI [3,4]
C0007222
UMLS CUI [4,1]
C0949214
UMLS CUI [4,2]
C0282111
UMLS CUI [4,3]
C0683877
UMLS CUI [4,4]
C0549177
UMLS CUI [4,5]
C0015576
UMLS CUI [4,6]
C1298908
UMLS CUI [4,7]
C1512693
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Similar models

Eligibility Criteria

6 forms
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. The subject consent data table contains subject IDs and consent information.
    3. This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, subjects's sex, twin IDs, and indicator for monozygotic and dizygotic twins.
    4. This data table contains 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.
    5. This subject phenotype table includes subject's sex, age at enrollment, race (n=3 variables; self-reported, race/ethnicity grouped by researcher, and genetically similar population groups), heart diagnoses (n=5 variables; primary diagnoses and classification, other diagnoses, comments, and disease ontology), IPSCORE IDs, and indicators if subject was part of a study/paper (n=10 variables; iPSCORE resource, aberrant iPSC methylation in twins, WGS, eQTL, allele-specific NKX2-5 binding in iPSC-CMs, Hi-C in iPSCs and iPSC-CMs, mutational burden of iPSCs, iPSC-derived retinal pigment epithelium, structural variation in IPSCORE, and lncrnas in iPSC-CMs).
    6. This sample attributes table includes sample histological type, tumor status, analyte type, sample source, other IDs (UCSD source tissue, UCSD iPSC clone, WiCell), sequencing center, clone and passage.
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion and exclusion criteria
C1512693 (UMLS CUI [1,1])
C0680251 (UMLS CUI [1,2])
Elig.phs001325.v3.p1.1
Item
The iPSCORE study had three recruiting approaches: 1) We targeted the recruitment of twins (monozygotic and dizygotic) and their immediate families from a southern California twin registry; 2) We worked with physicians to refer subjects (and their family members) into the study based on a diagnosed cardiovascular disease. In all cases where a physician referred an individual, the clinical diagnosis is provided; 3) Through advertisement on the internet and via fliers, we targeted the recruitment of large families, independent of the presence of twins or individuals with cardiovascular disease.
boolean
C0242800 (UMLS CUI [1,1])
C0242800 (UMLS CUI [2,1])
C0041427 (UMLS CUI [2,2])
C0015576 (UMLS CUI [2,3])
C0034975 (UMLS CUI [2,4])
C0031831 (UMLS CUI [3,1])
C0205543 (UMLS CUI [3,2])
C0011900 (UMLS CUI [3,3])
C0007222 (UMLS CUI [3,4])
C0949214 (UMLS CUI [4,1])
C0282111 (UMLS CUI [4,2])
C0683877 (UMLS CUI [4,3])
C0549177 (UMLS CUI [4,4])
C0015576 (UMLS CUI [4,5])
C1298908 (UMLS CUI [4,6])
C1512693 (UMLS CUI [4,7])
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