|
Status |
Public on Sep 08, 2020 |
Title |
11-wt-k36me2-2 |
Sample type |
SRA |
|
|
Source name |
CD8+ splenic T cells
|
Organism |
Mus musculus |
Characteristics |
strain: C57BL/6 cell type: CD8+ splenic T cells genotype: WT chip antibody: H3K36me2 (Millipore; Cat# 07-024; RRID: AB_310484)
|
Extracted molecule |
genomic DNA |
Extraction protocol |
CD8+ splenic T cells from wildtype and cTKO animals were isolated by flow cytometry, and ChIP-seq using anti-H3K27me3 and anti-H3K36me2 antibodies was performed see https://doi.org/10.1038/ncomms7033
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|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 4000 |
|
|
Data processing |
Sequencing and base calling was performed by GeneWiz (https://www.genewiz.com/) ChIP-seq reads were aligned to the mm10 genome assembly using bowtie2 with default parameters THOR from the Regulatory Genomics Toolbox ( https://www.regulatory-genomics.org/thor-2) was used to generate postprocessed ChIP-seq signal (in bigWig format) , after normalization to housekeeping genes. Genome_build: mm10 (GENCODE Release M20 (GRCm38.p6)) Supplementary_files_format_and_content: bigWig: postprocessed ChIP-seq signal from THOR pipeline; bed: bed files with coordinates of control regions used for normalization.
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|
|
Submission date |
Nov 29, 2019 |
Last update date |
Sep 09, 2020 |
Contact name |
Boris Bartholdy |
Organization name |
Albert Einstein College of Medicine
|
Department |
Cell Biology
|
Street address |
1300 Morris Park Ave
|
City |
Bronx |
State/province |
NY |
ZIP/Postal code |
10461 |
Country |
USA |
|
|
Platform ID |
GPL21103 |
Series (2) |
GSE141185 |
H1 linker histones regulate the balance of repressive and active chromatin domains via localized genomic compaction [ChIP-seq] |
GSE141187 |
H1 linker histones regulate the balance of repressive and active chromatin domains via localized genomic compaction |
|
Relations |
BioSample |
SAMN13429278 |
SRA |
SRX7241837 |