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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.
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Overall design |
Refer to individual Series
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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 |
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Platforms (2) |
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Samples (7)
|
GSM4195039 |
iPSC-derived neural cell PRDM8-/- derived from wildtype 1 |
GSM4195040 |
iPSC-derived neural cell PRDM8+/- derived from wildtype 1 |
GSM4195041 |
SAMPLE 1_iPSC-derived neural cell wildtype |
GSM4195042 |
SAMPLE 2_iPSC-derived neural cell PRDM8-/- |
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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. |
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Relations |
BioProject |
PRJNA592127 |