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Accession: PRJNA949263 ID: 949263

Whole Exome Sequencing of IOP family members

Idiopathic osteoporosis (IOP) is a rare form of early onset osteoporosis diagnosed in patients with no known metabolic or hormonal cause of bone loss. More...
AccessionPRJNA949263
Data TypeRaw sequence reads
ScopeMultispecies
SubmissionRegistration date: 27-Mar-2023
Columbia University Medical Center
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments9
Other datasets
BioSample9
SRA Data Details
ParameterValue
Data volume, Gbases118
Data volume, Mbytes76708

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