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Accession: PRJNA915310 ID: 915310

Whole-exome sequencing for disease gene identification

Identification of a novel gene for mosaic variegated aneuploidy
AccessionPRJNA915310
Data TypeRaw sequence reads
ScopeMultispecies
Grants
  • "Identification of novel causes and mechanisms for monogenic disorders" (Grant ID SBZH1, Dr. Senckenbergische Stiftung)
SubmissionRegistration date: 23-Dec-2022
Senckenberg Centre for Human Genetics
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments3
Other datasets
BioSample3
SRA Data Details
ParameterValue
Data volume, Gbases24
Data volume, Mbytes11040

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