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Series GSE141108 Query DataSets for GSE141108
Status Public on Aug 31, 2020
Title PRDM8 reveals aberrant DNA methylation in aging syndromes and is relevant for hematopoietic and neuronal differentiation.
Organism Homo sapiens
Experiment type Methylation profiling by genome tiling array
Expression profiling by high throughput sequencing
Summary This SuperSeries is composed of the SubSeries listed below.
 
Overall design Refer to individual Series
 
Citation(s) 32819411
Submission date Nov 27, 2019
Last update date Aug 31, 2020
Contact name Wolfgang Wagner
E-mail(s) [email protected]
Phone +49 241 8088611
Organization name RWTH Aachen University
Department Helmholtz Institute for Biomedical Engineering
Lab Stem Cell Biology and Cellular Engineering
Street address Pauwelsstrasse 20
City Aachen
ZIP/Postal code 52074
Country Germany
 
Platforms (2)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
GPL21145 Infinium MethylationEPIC
Samples (7)
GSM4195036 iPSC-derived neural cell wildtype 1
GSM4195037 iPSC-derived neural cell wildtype 2
GSM4195038 iPSC-derived neural cell wildtype 3
This SuperSeries is composed of the following SubSeries:
GSE141106 DNA methylation - PRDM8 reveals aberrant DNA methylation in aging syndromes and is relevant for hematopoietic and neuronal differentiation.
GSE141107 Gene expression - PRDM8 reveals aberrant DNA methylation in aging syndromes and is relevant for hematopoietic and neuronal differentiation.
Relations
BioProject PRJNA592127

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE141108_RAW.tar 231.6 Mb (http)(custom) TAR (of IDAT)
SRA Run SelectorHelp

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