|
Status |
Public on May 27, 2017 |
Title |
U87DOX whole genome bisulfite p8 |
Sample type |
SRA |
|
|
Source name |
Human glioblastoma cells
|
Organism |
Homo sapiens |
Characteristics |
tissue: Brain cell type: Human glioblastoma cells passage: in vitro for a long time
|
Treatment protocol |
for +Dox samples, cells were treated with doxycycline at 1 ug/ml for 48h
|
Growth protocol |
U87 cells grown in MEM +10% FCS medium
|
Extracted molecule |
genomic DNA |
Extraction protocol |
RNA was extracted for RNA-seq, genomic DNA was extracted for ChIP-seq and WGBS Library was constructed by microarray facility at Johns Hopkins University using commercially available kits (illumina)
|
|
|
Library strategy |
Bisulfite-Seq |
Library source |
genomic |
Library selection |
RANDOM |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
Tophat2 was used to map all RNA-seq reads to human genome (hg19) then Cufflink was employed to summarize the gene/transcript expression based on mapped reads. KLF4 ChIP-Seq data were mapped by Bowtie2, followed by MACS 1.4 being used to call peaks with cutoff of p < 1E-5 The peaks of H3K27ac was recognized by MACS2 as broad peaks based on their ChIP-Seq data mapped by Bowtie2. The cutoff of broad peak call was q < 0.1. An R package, DEGseq, was taken on RNA-seq data to identify differentially expressed genes (DEGs) for p < 0.001 between 0 hr and 48 hr in KLF4 WT and R458A cells, respectively. WGBS were aligned using Bismark, context-dependent methylation were extracted using bismark_methylation_extractor from merged bam files and format with coverage2cytosine. Genome_build: hg19
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|
|
Submission date |
Apr 11, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Shuli Xia |
E-mail(s) |
xia@kennedykriger.org
|
Phone |
443-923-9498
|
Organization name |
Kennedy Krieger Institute
|
Street address |
707 N Broadway
|
City |
Baltimore |
State/province |
Maryland |
ZIP/Postal code |
21205 |
Country |
USA |
|
|
Platform ID |
GPL11154 |
Series (1) |
GSE97632 |
Methylation DNA mediated KLF4 binding activity in glioblastoma cells |
|
Relations |
BioSample |
SAMN06706921 |
SRA |
SRX2732480 |