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Accession: PRJNA472118 ID: 472118

NHLBI TOPMed: Boston-Brazil Collaborative Project for Whole Genome Sequencing of Sickle Cell Disease Patients (human)

See Genome Information for Homo sapiens
This study involves sequencing of patients with a diagnosis of sickle cell disease from Brazil. No exclusionary criteria were employed and any eligible patients that consented to this study were recruited.
AccessionPRJNA472118; dbGaP: phs001599
TypeUmbrella project (Subtype:Authorized Access)
OrganismHomo sapiens[Taxonomy ID: 9606]
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens
SubmissionRegistration date: 19-May-2018
NHLBI
RelevanceMedical
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments387
Other datasets
BioSample387
SRA Data Details
ParameterValue
Data volume, Gbases50,071
Data volume, Tbytes7.42
NHLBI TOPMed: Boston-Brazil Collaborative Project for Whole Genome Sequencing of Sickle Cell Disease Patients encompasses the following sub-project:
Project TypeNumber of Projects
Phenotype or Genotype1
BioProject
accession
OrganismTitle
PRJNA472119Homo sapiensNHLBI TOPMed: Boston-Brazil Collaborative Project for Whole Genome Sequencing of Sickle Cell Disease Patients (BOSTON CHILDREN'S HOSPITAL)

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