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Accession: PRJNA517482 ID: 517482

Germline selection of Noonan syndrome mutations

We used next generation deep sequencing to study the spatial distribution of Noonan syndrome (NS) mutations in testes. More...
AccessionPRJNA517482
Data TypeRaw sequence reads
ScopeMultispecies
Grants
  • "Genetic Analysis Using Sperm Typing" (Grant ID R01 GM036745, National Institute of General Medical Sciences)
  • "Genetic Analysis Using Sperm Typing" (Grant ID R01 GM036745, National Institute of General Medical Sciences)
SubmissionRegistration date: 28-Jan-2019
University of Southern California
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments3
Other datasets
BioSample3
SRA Data Details
ParameterValue
Data volume, Gbases200
Data volume, Mbytes88165

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