|
Status |
Public on Mar 20, 2021 |
Title |
M36-Entorhinal Cortex (array) |
Sample type |
genomic |
|
|
Source name |
Entorhinal Cortex
|
Organism |
Mus musculus |
Characteristics |
mouse_id: M36 sentrix_id: 204027420027_R01C01 Sex: F group: 1 tissue: Entorhinal Cortex
|
Treatment protocol |
Mice were terminally anaesthetized with pentobarbital (intraperitoneal injection) and transcardially perfused with phosphate-buffered saline (PBS). The entorhinal cortex was dissected from the left brain hemisphere on wet ice and snap-frozen on dry ice for subsequent analysis
|
Growth protocol |
Animals were housed under standard conditions (constant temperature and humidity) with a 12h light/dark cycle in individually ventilated cages, with free access to food (Teklad irradiated global rodent diet (Envigo, United Kingdom)) and water.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA from all samples was isolated from the entorhinal cortex using the AllPrep DNA/RNA Mini Kit (Qiagen)
|
Label |
cy3, cy5
|
Label protocol |
DNA methylation was measured using the the Mammalian Methylation Array (HorvathMammalMethylChip4, GEO: GPL28271)
|
|
|
Hybridization protocol |
Standard Illumina protocols
|
Scan protocol |
Illumina HiScan
|
Data processing |
Normalized Average Beta calculated using the SeSame package in R
|
|
|
Submission date |
Mar 19, 2021 |
Last update date |
Mar 20, 2021 |
Contact name |
Emma Walker |
E-mail(s) |
e.m.walker@exeter.ac.uk
|
Organization name |
University of Exeter
|
Street address |
RILD Barrack Rd
|
City |
Exeter |
ZIP/Postal code |
EX2 5DW |
Country |
United Kingdom |
|
|
Platform ID |
GPL28271 |
Series (2) |
GSE169218 |
Characterizing the properties of bisulfite sequencing data: maximizing power and sensitivity to identify differences in DNA methylation [Array] |
GSE169235 |
Characterizing the properties of bisulfite sequencing data: maximizing power and sensitivity to identify differences in DNA methylation |
|