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Status |
Public on Sep 24, 2019 |
Title |
MEK and GSK3Ī² inhibition drives ES cells into a naive pluripotent state irrespective of their global methylation statusĀ |
Organism |
Mus musculus |
Experiment type |
Methylation profiling by high throughput sequencing Genome binding/occupancy profiling by high throughput sequencing
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Summary |
We carry out methyl DNA immunoprecipitation (meDIP), hydroxymethyl DNA immunoprecipitaion (hmeDIP) and H3K27me3 chromatin imminoprecipitation (ChIP) prior to sequencing on the Ion Proton semiconductor sequencing platform to report on the genome-wide epigenetic patterns in J1 mESC and mutant mESCs (hyper active DNMT3b/3l or DNMT1/3a/3b triple knock out) grown under serum conditions or in 2i meadia for 14 days
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Overall design |
Genome-wide patterns were generate on the Ion Proton P1 sequencer.
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Contributor(s) |
Thomson JP, Shukla R, Mjoseng H, Fawkes A, Clark R, Murphy L, Meehan RR |
Citation missing |
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Submission date |
Aug 31, 2015 |
Last update date |
Jul 25, 2021 |
Contact name |
John Paterson Thomson |
E-mail(s) |
john.thomson@igmm.ed.ac.uk
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Organization name |
University of Edinburgh
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Department |
MRC Human Genetics Unit
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Lab |
Meehan
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Street address |
Crewe Road
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City |
Edinburgh |
ZIP/Postal code |
EH4 2XU |
Country |
United Kingdom |
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Platforms (1) |
GPL18635 |
Ion Torrent Proton (Mus musculus) |
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Samples (20)
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Relations |
BioProject |
PRJNA294321 |
SRA |
SRP063019 |