Engelsk

This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, subjects's sex, and family group ethnicity.

9 Formulär  
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. The subject consent data table includes subject IDs, consent information, and subject aliases.
    3. This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, subjects's sex, and family group ethnicity.
    4. This subject sample mapping data table includes 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.
    5. Family Subject Phenotypes (WGS) year 1: AD affection status, Braak stage, presence of APOE allele combinations, availability of autopsy material, and general sociodemographic (race and ethnicity) data of participants for whom whole genome sequencing (WGS) data are available.
    6. This sample attributes table includes body site where sample was collected, analyte type, tumor status, and sequencing center.
    7. Connecting Family Subject Phenotypes year 1: participants' family members' AD affection status, Braak stage, APOE allele presence, availability of autopsy material, and general sociodemographic data (race and ethnicity).
    8. Case Control Enriched Phenotypes (WES) year 0: prevalent and incident AD status, AD diagnosis, selection criteria, age (n=2 variables; baseline, onset or last exam), APOE genotype, availability of autopsy data, Braak stage, and general sociodemographic (race and ethnicity) of participants for whom whole exome sequencing (WXS) data are available.
    9. Case Control Enriched Phenotypes (WES) year 1: prevalent and incident AD status, AD diagnosis, selection criteria, age (n=2 variables; baseline, onset or last exam), APOE genotype, availability of autopsy data, Braak stage, and general sociodemographic (race and ethnicity) of participants for whom whole exome sequencing (WXS) data are available.
pht003391
Beskrivning

pht003391

ADSP ID
Beskrivning

SUBJID

Datatyp

text

Alias
UMLS CUI [1,1]
C2348585
ADSP Family ID
Beskrivning

FamID

Datatyp

text

Alias
UMLS CUI [1,1]
C0015576
UMLS CUI [1,2]
C2349022
Father ADSP ID
Beskrivning

Father

Datatyp

text

Alias
UMLS CUI [1,1]
C0015671
UMLS CUI [1,2]
C2348585
Mother ADSP ID
Beskrivning

Mother

Datatyp

text

Alias
UMLS CUI [1,1]
C0026591
UMLS CUI [1,2]
C2348585
Sex
Beskrivning

Sex

Datatyp

text

Alias
UMLS CUI [1,1]
C0079399
Grouping variable indicating ethnic group of family
Beskrivning

FamGrp

Datatyp

text

Alias
UMLS CUI [1,1]
C0015031
Tillbaka till toppen

Similar models

This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, subjects's sex, and family group ethnicity.

9 Formulär
  1. StudyEvent: SEV1
    1. Eligibility Criteria
    2. The subject consent data table includes subject IDs, consent information, and subject aliases.
    3. This pedigree data table contains family relationships in the format of family IDs, subject IDs, father IDs, mother IDs, subjects's sex, and family group ethnicity.
    4. This subject sample mapping data table includes 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.
    5. Family Subject Phenotypes (WGS) year 1: AD affection status, Braak stage, presence of APOE allele combinations, availability of autopsy material, and general sociodemographic (race and ethnicity) data of participants for whom whole genome sequencing (WGS) data are available.
    6. This sample attributes table includes body site where sample was collected, analyte type, tumor status, and sequencing center.
    7. Connecting Family Subject Phenotypes year 1: participants' family members' AD affection status, Braak stage, APOE allele presence, availability of autopsy material, and general sociodemographic data (race and ethnicity).
    8. Case Control Enriched Phenotypes (WES) year 0: prevalent and incident AD status, AD diagnosis, selection criteria, age (n=2 variables; baseline, onset or last exam), APOE genotype, availability of autopsy data, Braak stage, and general sociodemographic (race and ethnicity) of participants for whom whole exome sequencing (WXS) data are available.
    9. Case Control Enriched Phenotypes (WES) year 1: prevalent and incident AD status, AD diagnosis, selection criteria, age (n=2 variables; baseline, onset or last exam), APOE genotype, availability of autopsy data, Braak stage, and general sociodemographic (race and ethnicity) of participants for whom whole exome sequencing (WXS) data are available.
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
pht003391
SUBJID
Item
ADSP ID
text
C2348585 (UMLS CUI [1,1])
FamID
Item
ADSP Family ID
text
C0015576 (UMLS CUI [1,1])
C2349022 (UMLS CUI [1,2])
Father
Item
Father ADSP ID
text
C0015671 (UMLS CUI [1,1])
C2348585 (UMLS CUI [1,2])
Mother
Item
Mother ADSP ID
text
C0026591 (UMLS CUI [1,1])
C2348585 (UMLS CUI [1,2])
Item
Sex
text
C0079399 (UMLS CUI [1,1])
Sex
Code List
Sex
CL Item
Male (1)
CL Item
Female (2)
Item
Grouping variable indicating ethnic group of family
text
C0015031 (UMLS CUI [1,1])
FamGrp
Code List
Grouping variable indicating ethnic group of family
CL Item
Caucasian (1)
CL Item
Dominican (2)
CL Item
Dutch Isolate (3)
CL Item
African American (4)
CL Item
Puerto Rican (5)
CL Item
Not Applicable (NA)
Tillbaka till toppen