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Multi-omics profiling reveals convergent MAGEL2-driven defects in human corticogenesis across Prader-Willi and Schaaf-Yang syndromes.

geo / GSE329288

Dataset

Provider
GEO
Type
bulk
Organism
Homo sapiens (tax 9606)
Format / file
counts_table — GSE329288_salmon.merged.gene_counts.tsv.gz (1.82 MB)
Matrix
42 samples
Source page
https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE329288
Download URL
https://ftp.ncbi.nlm.nih.gov/geo/series/GSE329nnn/GSE329288/suppl/GSE329288_salmon.merged.gene_counts.tsv.gz

Publication and identifiers

DOIs

None

PubMed IDs

Accessions

  • geo_series: GSE329288
  • bioproject: PRJNA1458290

ASAP projects

Not in ASAP yet.