|
Status |
Public on Feb 15, 2018 |
Title |
exp_succinyllysine_rep_1 |
Sample type |
SRA |
|
|
Source name |
immortalized mouse embryonic fibroblast cell line
|
Organism |
Mus musculus |
Characteristics |
cell line: R26M2rtTA/+;TetOcre;Sdhcfl/fl day: 16 antibody: anti-succinyllysine (PTM Biolabs cat# PTM-401)
|
Treatment protocol |
Gene rearrangement induced by adding doxycycline to media at 1 microgram/mL final concentration.
|
Growth protocol |
Cells grown in DMEM (low glucose) containing 10% FBS at 37 degrees Celsius in 5% CO2.
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Cells harvested by trypsinization and fixed with formaldehyde prior to lysis. Chromatin prepared via MNase digestion and sonication. Either ChIP-enriched chromatin or non-enriched input chromatin used for library construction. ThruPLEX DNA-seq 48D Kit (Rubicon Genomics cat# R400406)
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 4000 |
|
|
Description |
processed data file: succinyllysine_peaks.bed
|
Data processing |
Illumina Casava1.7 software used for basecalling. Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence, then mapped to mm10 whole genome using bowtie v2.2.3 Peaks were called with MACS Genome_build: mm10 Supplementary_files_format_and_content: bed files with peaks summarized across replicates and treatments and bedgraph files for each sample.
|
|
|
Submission date |
Sep 27, 2017 |
Last update date |
May 15, 2019 |
Contact name |
John Andrew Smestad |
Organization name |
Mayo Clinic
|
Department |
Biochemistry and Molecular Biology
|
Lab |
Louis (Jim) Maher
|
Street address |
200 1st St. SW
|
City |
Rochester |
State/province |
Minnesota |
ZIP/Postal code |
55905 |
Country |
USA |
|
|
Platform ID |
GPL21103 |
Series (2) |
GSE104362 |
iMEF SDHC-loss ChIP-seq |
GSE129956 |
Functional genomics of iMEF SDHC-loss stable line |
|
Relations |
BioSample |
SAMN07714770 |
SRA |
SRX3227364 |