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Accession: PRJNA288100 ID: 288100

Homo Sapiens (human)

Homo Sapiens Exome

See Genome Information for Homo sapiens
This study is to identify novel variants causing late-onset, non-syndromic hearing loss and vestibular dysfunction
AccessionPRJNA288100
Data TypeExome
ScopeMonoisolate
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 25-Jun-2015
Yonsei University College of Medicine
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments2
Other datasets
BioSample2
SRA Data Details
ParameterValue
Data volume, Gbases33
Data volume, Mbytes14276

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