|
Status |
Public on Apr 08, 2016 |
Title |
INPUT ChIP-seq GH1003 |
Sample type |
SRA |
|
|
Source name |
ZR-75-1 breast cancer cell line
|
Organism |
Homo sapiens |
Characteristics |
cell line: ZR-75-1 cell type: Ascites from a ductal carcinoma of the breast treatment: Dexamethasone and 17β-estradiol concentration: 100nM time: 30 minutes replicate: replicate 1 antibody: FoxA1 ab23738 Abcam growth proptocol: For maintenance cells were cultured in RPMI containing 2mM L-glutamine supplemented 10% calf serum, 1mM sodium pyruvate, 1X non-essential amino acids, and 1% penicillin-streptomycin
|
Treatment protocol |
Cells were plated for experiments in phenol red free growth medium supplemented with 10% charcoal-dextran serum twenty-four hours before hormone treatment. Cells were left untreated or induced with 100nM dexamethasone or 100nM estradiol for 30 minutes.
|
Growth protocol |
see additional columns of the SAMPLES section
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Lysates were clarified from sonicated nuclei and GR/DNA, ER/DNA, of FoxA1/DNA complexes were isolated with antibody.
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|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
RTA 1.12.42 was used for Basecalling and Casava 1.8.2 ws used for demultiplexing. Alignment was performed by Bowtie2 software with the hg19 reference genome. Areas of enrichment were identified using DNase2Hotspots software(http://sorceforge.net/proujects/dnase2hotspots/) software with FDR 0%. Raw signal density graphs were generated by counting tags at each genomic coordinate after extending the length of sequences to 150bp by strands. Values for tag densities were normalized to 10 million reads to adjust for differences in the sequencing depth between samples. Genome_build: hg19 Supplementary_files_format_and_content: comma-delimited (CSV) text files include genomic locations (Chromosome, start, end ), z-score, p-value and the maximum density of hotspots. Bedgraph files contain genomic locations and normalized tag density profiles.
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|
|
Submission date |
Aug 20, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Songjoon Baek |
Organization name |
NCI / NIH
|
Department |
CCR
|
Lab |
LRBGE
|
Street address |
41 Library Drive
|
City |
Bethesda |
State/province |
MD |
ZIP/Postal code |
20892 |
Country |
USA |
|
|
Platform ID |
GPL11154 |
Series (2) |
GSE72249 |
Characterization of ER, GR, and FoxA1 binding patterns in breast cancer cells treated with either Dex or E2 |
GSE72252 |
DNaseI hypersensitivity assay and ER, GR, and FoxA1 binding patterns in breast cancer cells |
|
Relations |
BioSample |
SAMN04004039 |
SRA |
SRX1161193 |