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This subject consent data table includes subject IDs, consent group information, and subject aliases.

5 Formulär  
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. This subject consent data table includes subject IDs, consent group information, and subject aliases.
    3. This subject sample mapping data table includes a mapping of study subject IDs to sample IDs and sample aliases. 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.
    4. This subject phenotypes data table includes participants who have completed questionnaires regarding medical history, medications, physical activity, diet, alcohol intake, and cigarette smoking. Objective measures of anthropometric, neuromuscular, vision, strength, and cognitive variables were obtained at a clinic visit. Skeletal assessments included DEXA of the total hip, femoral neck and lumbar spine, calcaneal ultrasound, and vertebral radiographs. Radiographic prevalent and incident vertebral (baseline to visit 3) fractures were assessed. Sleep characteristics were assessed in a subcohort with actigraphy and polysomnography. Radiographic hip osteoarthritis was measured using hip X-rays collected at the SOF baseline visit and a modified Croft summary grade for radiographic hip OA (RHOA) severity of 0 - 4 was assigned to each hip based on individual radiographic features. Both SOF and MrOS data contain harmonized variables with the prefix HA to allow sex differences to be evaluated.
    5. This sample attributes data table includes body site where sample was collected, analyte type, and tumor status.
pht010695
Beskrivning

pht010695

Alias
UMLS CUI [1,1]
C3846158
Harmonized SOF ID
Beskrivning

SUBJECT_ID

Datatyp

string

Alias
UMLS CUI [1,1]
C2348585
Consent group
Beskrivning

CONSENT

Datatyp

text

Alias
UMLS CUI [1,1]
C0021430
Source repository where subjects originate (Coriell)
Beskrivning

SUBJECT_SOURCE

Datatyp

string

Alias
UMLS CUI [1,1]
C3847505
UMLS CUI [1,2]
C0449416
UMLS CUI [1,3]
C0681850
Subject ID used in the Source Repository
Beskrivning

SOURCE_SUBJECT_ID

Datatyp

string

Alias
UMLS CUI [1,1]
C2348585
UMLS CUI [1,2]
C3847505
UMLS CUI [1,3]
C0449416
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This subject consent data table includes subject IDs, consent group information, and subject aliases.

5 Formulär
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. This subject consent data table includes subject IDs, consent group information, and subject aliases.
    3. This subject sample mapping data table includes a mapping of study subject IDs to sample IDs and sample aliases. 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.
    4. This subject phenotypes data table includes participants who have completed questionnaires regarding medical history, medications, physical activity, diet, alcohol intake, and cigarette smoking. Objective measures of anthropometric, neuromuscular, vision, strength, and cognitive variables were obtained at a clinic visit. Skeletal assessments included DEXA of the total hip, femoral neck and lumbar spine, calcaneal ultrasound, and vertebral radiographs. Radiographic prevalent and incident vertebral (baseline to visit 3) fractures were assessed. Sleep characteristics were assessed in a subcohort with actigraphy and polysomnography. Radiographic hip osteoarthritis was measured using hip X-rays collected at the SOF baseline visit and a modified Croft summary grade for radiographic hip OA (RHOA) severity of 0 - 4 was assigned to each hip based on individual radiographic features. Both SOF and MrOS data contain harmonized variables with the prefix HA to allow sex differences to be evaluated.
    5. This sample attributes data table includes body site where sample was collected, analyte type, and tumor status.
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
pht010695
C3846158 (UMLS CUI [1,1])
SUBJECT_ID
Item
Harmonized SOF ID
string
C2348585 (UMLS CUI [1,1])
Item
Consent group
text
C0021430 (UMLS CUI [1,1])
CONSENT
Code List
Consent group
CL Item
Subjects did not participate in the study, did not complete a consent document and are included only for the pedigree structure and/or genotype controls, such as HapMap subjects (0)
C5418626 (UMLS CUI [1,1])
C0549184 (UMLS CUI [1,2])
C0009797 (UMLS CUI [1,3])
C0205257 (UMLS CUI [1,4])
C2700399 (UMLS CUI [1,5])
C0017431 (UMLS CUI [1,6])
C4553389 (UMLS CUI [1,7])
C5418626 (UMLS CUI [2,1])
C0549184 (UMLS CUI [2,2])
C0009797 (UMLS CUI [2,3])
C0205257 (UMLS CUI [2,4])
C2700399 (UMLS CUI [2,5])
C0030761 (UMLS CUI [2,6])
CL Item
Disease-Specific (Aging Related 1, RD) (DS-AGR1-RD) (1)
C0021430 (UMLS CUI [1,1])
C0205369 (UMLS CUI [1,2])
C0012634 (UMLS CUI [1,3])
SUBJECT_SOURCE
Item
Source repository where subjects originate (Coriell)
string
C3847505 (UMLS CUI [1,1])
C0449416 (UMLS CUI [1,2])
C0681850 (UMLS CUI [1,3])
SOURCE_SUBJECT_ID
Item
Subject ID used in the Source Repository
string
C2348585 (UMLS CUI [1,1])
C3847505 (UMLS CUI [1,2])
C0449416 (UMLS CUI [1,3])
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