ID
45895
Beschreibung
Principal Investigator: Bernice Porjesz, PhD, SUNY Health Sciences Center, New York, NY, USA MeSH: Alcoholism https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000976 COGA is a family study of alcoholism, in which the subjects have been drawn from the Collaborative Study on the Genetics of Alcoholism (COGA), a large, ongoing family-based study that includes subjects from seven sites around the US. COGA has gathered detailed, standardized data on study participants, including diagnostic and neurophysiological assessments. This sample has already proved successful in identifying several genes that influence the risk for alcoholism and neurophysiological endophenotypes, which have been independently replicated. COGA data were included as part of two Genetic Analysis Workshops, and the phenotypes are familiar to the genetics community. Alcoholic probands were recruited from treatment facilities, assessed by personal interview, and after securing permission, other family members were also assessed. A set of comparison families was drawn from the same communities as the families recruited through an alcoholic proband. Assessment involved a detailed personal interview developed for this project, the Semi-Structured Assessment for the Genetics of Alcoholism (SSAGA), which gathers detailed information on alcoholism related symptoms along with other drugs and psychiatric symptoms. Many participants also came to the laboratories for electroencephalographic studies. Neurophysiological features that have been shown to be useful endophenotypes for which we have linkage and in some cases association results are included on a subset of the case-control sample: the beta power of the resting electroencephalogram (EEG), the P3(00) amplitude of the visual event-related potential (ERP), and the theta and delta event-related oscillations (EROs) underlying the P3. As part of COGA, a set of informative African American families were selected to have Genome-Wide Association data obtained within families. Genotyping was performed using the Illumina Omni2.5_080814_1 chip to genotype 3,438 subjects selected from densely affected families. Genotyping was performed at CIDR. This sample complements a set of densely affected European American families previously made available under dbGaP study accession phs000763. In addition, exome sequencing data on a subset of individuals with GWAS were added in version 2.
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- 08.12.23 08.12.23 - Simon Heim
Rechteinhaber
Bernice Porjesz, PhD, SUNY Health Sciences Center, New York, NY, USA
Hochgeladen am
8. Dezember 2023
DOI
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Creative Commons BY 4.0
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dbGaP phs000976 COGA: African American Family GWAS
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- The subject consent file includes subject IDs, consent information, and subject aliases.
- The subject pedigree table contains family ID, subject ID, father ID, mother ID, sex, and twin ID.
- This data table 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 subject phenotype file includes details of alcohol consumption related measurements, including age of first drink, when first experienced 'drunkeness', presence of tolerance and withdrawal symptoms, determination of DSM4 alcohol dependence, DSM5 alcohol use disorder (AUD) among subjects with regular/occasional alcohol consumption obtained through application of the SSAGA (Semi-Structured Assessment for the Genetics of Alcoholism), and values of theta Fz, in addition to basic sociodemographic data.
- This sample attributes table contains sample ID, body site where sample was collected, analyte type, and tumor status.
Ähnliche Modelle
Eligibility Criteria
- StudyEvent: SEV1
- Eligibility Criteria
- The subject consent file includes subject IDs, consent information, and subject aliases.
- The subject pedigree table contains family ID, subject ID, father ID, mother ID, sex, and twin ID.
- This data table 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 subject phenotype file includes details of alcohol consumption related measurements, including age of first drink, when first experienced 'drunkeness', presence of tolerance and withdrawal symptoms, determination of DSM4 alcohol dependence, DSM5 alcohol use disorder (AUD) among subjects with regular/occasional alcohol consumption obtained through application of the SSAGA (Semi-Structured Assessment for the Genetics of Alcoholism), and values of theta Fz, in addition to basic sociodemographic data.
- This sample attributes table contains sample ID, body site where sample was collected, analyte type, and tumor status.
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