Englisch

This sample attributes data table includes body site where sample was collected, analyte type, and tumor status.

5 Formulare  
  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.
pht010698
Beschreibung

pht010698

Alias
UMLS CUI [1,1]
C3846158
Sample ID
Beschreibung

SAMPLE_ID

Datentyp

string

Alias
UMLS CUI [1,1]
C1299222
Body site where sample was collected
Beschreibung

BODY_SITE

Datentyp

string

Alias
UMLS CUI [1,1]
C0449705
Analyte Type
Beschreibung

ANALYTE_TYPE

Datentyp

string

Alias
UMLS CUI [1,1]
C4744818
Tumor status
Beschreibung

IS_TUMOR

Datentyp

text

Alias
UMLS CUI [1,1]
C0475752
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Ähnliche Modelle

This sample attributes data table includes body site where sample was collected, analyte type, and tumor status.

5 Formulare
  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)
Datentyp
Alias
Item Group
pht010698
C3846158 (UMLS CUI [1,1])
SAMPLE_ID
Item
Sample ID
string
C1299222 (UMLS CUI [1,1])
BODY_SITE
Item
Body site where sample was collected
string
C0449705 (UMLS CUI [1,1])
ANALYTE_TYPE
Item
Analyte Type
string
C4744818 (UMLS CUI [1,1])
Item
Tumor status
text
C0475752 (UMLS CUI [1,1])
IS_TUMOR
Code List
Tumor status
CL Item
Is not a tumor (N)
CL Item
Is Tumor (Y)
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