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Accession: PRJNA517199 ID: 517199

Next generation rare variant discovery in multiplex AD families (human)

See Genome Information for Homo sapiens
Two multiplex for alcohol dependence family studies were initiated based on the gender of a pair of probands. Ascertainment of a pair of AD probands was used to increase the density of alcohol dependence within the family. Identification of male (Cognitive and Personality Factors in Relatives of Alcoholics Family Study) and female (Biological Risk Factors in Female Alcoholics Family Study) alcohol dependent probands was accomplished by identifying an alcohol dependent proband while in treatment in a substance abuse treatment facility in Pittsburgh and surrounding communities who provided contact information for a sibling whom he/she thought might be interested in participating. The studies had identical ascertainment requirements. DNA was banked for all willing participants.
AccessionPRJNA517199; dbGaP: phs001775
TypeUmbrella project (Subtype:Authorized Access)
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 25-Jan-2019
NIAAA
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments40
Other datasets
BioSample40
Genotype and Phenotype (dbGaP)1
SRA Data Details
ParameterValue
Data volume, Gbases446
Data volume, Tbytes0.22
Next generation rare variant discovery in multiplex AD families encompasses the following sub-project:
Project TypeNumber of Projects
Phenotype or Genotype1
BioProject
accession
OrganismTitle
PRJNA517200Homo sapiensNext generation rare variant discovery in multiplex AD families (UNIVERSITY OF PITTSBURGH...)

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