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High Frequency of CNV Mutations in Combined Schizophrenia and Epilepsy

GEO Series GSE23703. Homo sapiens. 506 samples. Type: 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

Topics