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Genome Information for Homo sapiens
Whole genome sequencing of SLE family trios where the proband is affected and the parents are unaffected used to find rare variants contributing to the risk of SLE.
| Accession | PRJNA476687 |
| Data Type | Genome sequencing, Phenotype or Genotype |
| Scope | Multiisolate |
| 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-Jun-2018
Uppsala University |
| Relevance | Medical |
Project Data:
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