geoopen

Integrated analysis of copy number variation-associated lncRNAs identifies candidates contributing to the etiologies of congenital kidney anomalies.

GEO Series GSE223312. Homo sapiens. 6 samples. Type: Expression profiling by high throughput sequencing.

ShareScore

24/100

Overall dataset sharing score

Score breakdown

These five areas show where the dataset supports — or may limit — practical reuse.

Stewardship: 4
Harmonization: 8
Access: 4
Reuse readiness: 0
Engagement: 8

Topics

Homo sapiens Expression profiling by high throughput sequencing GEO gene expression

Dataset details

Repository: geo
Published: May 1, 2023
License: GEO-Open
DOI: geo/GSE223312

Scored with release 0.9.0

ScienceDex for faculty

Your academic CV and NIH biosketch

Make your CV in your school's format and your NIH biosketch from it, then download both as Word files.

Start your CV How the NIH biosketch works