|
Status |
Public on May 24, 2022 |
Title |
ChIP_Control_Rep1_input |
Sample type |
SRA |
|
|
Source name |
mouse hippocampus area CA1
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6J Male mouse id: Mouse 1 condition: Home cage control
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Brains were collected from home cage controls or from mice who underwent fear conditioning 30 min before ChIP was conducted on Mnase digested tissue from area CA1 with antibodies against macroH2A1 (abcam cag#37264) or macroH2A2 (Abcam cat#3173) Library prep was conducted by Genome Quebec using NEBNext Ultra II library prep kit Adapters: IlluminaTruSeq LT
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 4000 |
|
|
Description |
Input
|
Data processing |
Reads were aligned using Bowtie 2. Peaks were identified using epic2 Differential analysis for macroH2A1 and macroH2A2 binding was assessed with DiffBind (v.2.10.0) Genome_build: UCSC mm10
|
|
|
Submission date |
Mar 24, 2020 |
Last update date |
May 24, 2022 |
Contact name |
Iva Toronto Zovkic |
E-mail(s) |
iva.zovkic@utoronto.ca
|
Phone |
9058283961
|
Organization name |
University of Toronto Mississauga
|
Street address |
3359 Mississauga Road North, CCT Building Room 4071
|
City |
Mississauga |
State/province |
Ontario |
ZIP/Postal code |
L5L1C6 |
Country |
Canada |
|
|
Platform ID |
GPL21103 |
Series (1) |
GSE147445 |
Histone variant macroH2A1 is a stronger regulator of hippocampal transcription and memory than macroH2A2 in mice |
|
Relations |
BioSample |
SAMN14437737 |
SRA |
SRX7980625 |