|
Status |
Public on Jun 01, 2017 |
Title |
FOXN3_iRIP-Seq_Rep1 |
Sample type |
SRA |
|
|
Source name |
MCF-7 Cell
|
Organism |
Homo sapiens |
Characteristics |
cell type: MCF-7
|
Treatment protocol |
Treated with antibodies against FOXN3.
|
Growth protocol |
Cells were maintained in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% fetal bovine serum (FBS) in a humidified incubator equilibrated with 5% CO2 at 37°C.
|
Extracted molecule |
total RNA |
Extraction protocol |
chloroform extraction One microliter of glycogen (10 mg/ml stock) was added and RNAs were precipitated by adding 3 volumes of ethanol and dissolved in 10.5 μl water. The recovered RNAs were used to generate paired-end sequencing library with Truseq small RNA library preparation kit (Illumina) following the manufacturer’s instruction.
|
|
|
Library strategy |
RIP-Seq |
Library source |
transcriptomic |
Library selection |
other |
Instrument model |
BGISEQ-500 |
|
|
Description |
iRIP-Seq data for FOXN3 replicate1.
|
Data processing |
base-calling: Phred. alignment: bowtie2 for ChIP-Seq; TopHat2 for RIP-Seq. peak-calling: MACS2 for ChIP-Seq; CIMS and Piranha for RIP-Seq. ChIPseeker for the annotation of peaks. Genome_build: ChIP-Seq: hg19; RIP-Seq: hg38. Supplementary_files_format_and_content: bigwig (bw): The signal intensity of binding. Bed files for RIP-Seq.
|
|
|
Submission date |
Jan 18, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Wanjin Li |
E-mail(s) |
[email protected]
|
Phone |
13622157177
|
Organization name |
Peking University Health Science Center
|
Street address |
No. 38, Xueyuan road.
|
City |
Beijing |
ZIP/Postal code |
100191 |
Country |
China |
|
|
Platform ID |
GPL23227 |
Series (2) |
GSE93780 |
FOXN3 and SIN3A ChIP-Seq; FOXN3 and IgG iRIP-Seq |
GSE93781 |
FOXN3 Enlists NEAT1-containing SIN3A Complex to Regulate Mammary Epithelium Differentiation and Promote Breast Cancer Metastasis |
|
Relations |
BioSample |
SAMN06238147 |
SRA |
SRX2582730 |