zenodoopen
Whole-genome sequencing reveals contribution of rare and common variation to structural kidney and urinary tract malformations
<p>Supplementary tables detailing analysis of whole-genome sequencing data from 992 patients with congenital anomalies of the kidneys and urinary tract (CAKUT). </p>
ShareScore
36/100
Overall dataset sharing score
Score breakdown
These five areas show where the dataset supports — or may limit — practical reuse.
- Stewardship
- 4
- Harmonization
- 4
- Access
- 20
- Reuse readiness
- 8
- Engagement
- 0