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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.
| Accession | PRJNA472118; dbGaP: phs001599 |
| Type | Umbrella project (Subtype:Authorized Access) |
| Organism | Homo sapiens[Taxonomy ID: 9606] Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo; Homo sapiens |
| Submission | Registration date: 19-May-2018 NHLBI |
| Relevance | Medical |
Project Data:
| Resource Name | Number of Links |
|---|
| Sequence data |
| SRA Experiments | 387 |
| Other datasets |
| BioSample | 387 |
NHLBI TOPMed: Boston-Brazil Collaborative Project for Whole Genome Sequencing of Sickle Cell Disease Patients encompasses the following sub-project:
| Project Type | Number of Projects |
| Phenotype or Genotype | 1 |
BioProject accession | Organism | Title |
|---|
| PRJNA472119 | Homo sapiens | NHLBI TOPMed: Boston-Brazil Collaborative Project for Whole Genome Sequencing of Sickle Cell Disease Patients (BOSTON CHILDREN'S HOSPITAL) |
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