To identify modifier gene variants that contribute to clinical outcome, we sequenced the exomes of individuals at both ends of a phenotype distribution (i.e., mild and severe cognitive condition).
| Accession | PRJNA391353 |
| Data Type | Raw sequence reads |
| Scope | Multispecies |
| Submission | Registration date: 21-Jun-2017
University of Arizona |
| Relevance | Medical |
Project Data:
| Resource Name | Number
of Links |
|---|
| Sequence data |
| SRA Experiments | 21 |
| Other datasets |
| BioSample | 21 |