geoopen
Rett syndrome-causing MECP2 mutations severely impact key cellular and molecular features of human astrocytes
GEO Series GSE185726. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.
ShareScore
20/100
Overall dataset sharing score
Score breakdown
These five areas show where the dataset supports — or may limit — practical reuse.
- Stewardship
- 4
- Harmonization
- 8
- Access
- 0
- Reuse readiness
- 0
- Engagement
- 8