Next generation rare variant discovery in multiple... (ID 517200) - BioProject

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Accession: PRJNA517200 ID: 517200

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

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Two multiplex for alcohol dependence family studies were initiated based on the gender of a pair of probands. More...

Accession	PRJNA517200; dbGaP: phs001775
Data Type	Phenotype or Genotype
Scope	Multiisolate
Organism	Homo sapiens[Taxonomy ID: 9606] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
Submission	Registration date: 25-Jan-2019 UNIVERSITY OF PITTSBURGH AT PITTSBURGH
Relevance	Medical

Project Data:

Resource Name	Number of Links
Sequence data
SRA Experiments	40
Other datasets
BioSample	40
Genotype and Phenotype (dbGaP)	1

Parameter	Value
Data volume, Gbases	446
Data volume, Tbytes	0.22

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