geoopen
Rare germline copy number variations and disease susceptibility in familial melanoma
GEO Series GSE85010. Homo sapiens. 254 samples. Type: Genome variation profiling by SNP array; Genome variation profiling by genome tiling array.
ShareScore
16/100
Overall dataset sharing score
Score breakdown
These five areas show where the dataset supports — or may limit — practical reuse.
- Stewardship
- 4
- Harmonization
- 4
- Access
- 4
- Reuse readiness
- 0
- Engagement
- 4