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Accession: PRJNA157229 ID: 157229

Homo sapiens (human)

Genetic Defects in familial renal disorders

See Genome Information for Homo sapiens
To be updated
AccessionPRJNA157229; dbGaP: phs000477
Data TypePhenotype or Genotype
ScopeMultiisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 30-Mar-2012
MASSACHUSETTS INSTITUTE OF TECHNOLOGY
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments31
Other datasets
BioSample31
Genotype and Phenotype (dbGaP)1
SRA Data Details
ParameterValue
Data volume, Gbases213
Data volume, Tbytes0.11

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