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Accession: PRJNA954058 ID: 954058

Whole-genome sequencing for 48 children with hereditary pathology a joint pilot project between the UMC CF and the NLA PI (contract DPMRV-1986/161-20 dated 09.12.2021)

The aim of the project was to identify and evaluate genetic variants based on whole-genome sequencing in children with early onset epilepsy and osteogenesis imperfecta in Kazakhstan.
AccessionPRJNA954058
Data TypeRaw sequence reads
ScopeMultispecies
SubmissionRegistration date: 10-Apr-2023
University Medical Center Corporate Fund; PI National Laboratory Astana, Nazarbayev University
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments6
Other datasets
BioSample6
SRA Data Details
ParameterValue
Data volume, Gbases659
Data volume, Tbytes0.23

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