|
Status |
Public on Jun 12, 2017 |
Title |
shLuc -Glucose H3K9ac ChIPseq |
Sample type |
SRA |
|
|
Source name |
Hep3B cells_ChIP
|
Organism |
Homo sapiens |
Characteristics |
antibody: anti-H3K9ac, Active Motif, 39917 cell line: Hep3B shRNA: Luc
|
Treatment protocol |
glucose starvation in DMEM medium without glucose, then treat with glucose (4.5g/L)
|
Growth protocol |
culture in DME/F12 medium
|
Extracted molecule |
genomic DNA |
Extraction protocol |
ChIP-IT High Sensitivity kit (Active motif) according to the manufacturer’s manual Prepared using DNA Library preparation kit (KAPA, KK8232), as per the manufacturer’s protocol. In brief, DNA was fragmented to a median size of 150bp by sonication. Fragmented DNA ends were polished and 5′-phosphorylated. After addition of 3′-A to the ends, indexed Y-adapters were ligated and the samples were PCR amplified.
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
BCL files containing the sequence data were converted into “.fastq.gz” files and individual sample libraries were demultiplexed using CASAVA 1.8.2 with no mismatches. 3 nts from both ends were trimmed off and aligned to hg19 human assembly by Bowtie2. sam files converted to bam files Genome_build: hg19 Supplementary_files_format_and_content: bigwig files were generated by bamcompare in Deeptools and normailzed to 1X genome coverage
|
|
|
Submission date |
Feb 26, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Xian Zhang |
E-mail(s) |
zhangxian1987@gmail.com
|
Organization name |
MSKCC
|
Street address |
580 main st apt 138
|
City |
New York |
ZIP/Postal code |
10044 |
Country |
USA |
|
|
Platform ID |
GPL11154 |
Series (2) |
GSE66340 |
H3K9ac occupancy of Nedd4- or control-knockdown Hep3B cells |
GSE66342 |
Gene expression profiling and H3K9ac occupancy in Nedd4 knockdown Hep3B cells |
|
Relations |
BioSample |
SAMN03378741 |
SRA |
SRX892618 |