A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging - - GEO DataSets - NCBI

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A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging

(Submitter supplied) Our data throw light upon the effect of WRN deficiency on gene expression and epigenomic modification, which indicates aging-associated changes from both genomic and epigenomic level.

Organism:: Homo sapiens

Type:: Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing; Methylation profiling by high throughput sequencing

Platforms:: GPL11154 GPL16791
22 Samples

Download data: BED, BEDGRAPH, TXT

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Accession:: GSE52285

ID:: 200052285

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GEO DataSet Links for BioProject (Select 227344) (1)
GEO DataSets
A Werner syndrome stem cell model unveils heterochromatin alterations as a drive...
A Werner syndrome stem cell model unveils heterochromatin alterations as a driver of human aging
Accession: GSE52285

GEO DataSets
txid57494[Organism] (158349)
Protein
PREDICTED: Homo sapiens centrosomal protein 192 (CEP192), transcript variant X15...
PREDICTED: Homo sapiens centrosomal protein 192 (CEP192), transcript variant X15, mRNA
gi|2217316993|ref|XM_047437570.1|

Nucleotide
PREDICTED: Homo sapiens zinc finger protein 292 (ZNF292), transcript variant X9,...
PREDICTED: Homo sapiens zinc finger protein 292 (ZNF292), transcript variant X9, mRNA
gi|2462607159|ref|XM_054354803.1|

Nucleotide

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