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Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders [ChIP-seq]

GEO Series GSE210465. Homo sapiens. 18 samples. Type: Genome binding/occupancy 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

Topics