|
Status |
Public on Jan 29, 2018 |
Title |
BE2C_H3K27ME3 |
Sample type |
SRA |
|
|
Source name |
BE(2)-C_Neuroblastoma
|
Organism |
Homo sapiens |
Characteristics |
cell line: BE(2)-C cell type: neuroblastoma cell line growth condition: 10% FBS, DMEM treated with: None chip antibody: H3K27me3 chip antibody vendor: abcam chip antibody catalog #: ab6002 input: BE2C_INPUT barcode: ACAGTG
|
Treatment protocol |
Tet-Off MYCN shutdown was performed by addition of doxycycline (0.2μg/mL) to growth media
|
Growth protocol |
SK-N-AS, SH-SY5Y, NGP, BE(2)-C, and KELLY cells were kindly provided by Dr. Kimberly Stegmaier (Dana Farber Cancer Institute) and cultured in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with 10% FBS. SHEP-21N cells were kindly provided by Dr. William Weiss (University of California, San Francisco) and cultured in RPMI supplemented with 10% Tetracycline-Free FBS (Clontech). Tet-Off MYCN shutdown was performed by addition of doxycycline (0.2μg/mL) to growth media
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. Libraries were prepared using the Rubicon Thruplex FD library preparation kit (cat#: 400427) per manufacturers instructions.
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
|
|
Description |
Chromatin IP against BRD4 in BE(2)-C
|
Data processing |
Sequenced reads were aligned to HG19 referenece genome using bowtie2 with default parameters with the exception of '-k 1' Peaks were called using MACS1.4.2 with p-val =1e-9 and background datasets as described in characteristic: input Genome_build: hg19 Supplementary_files_format_and_content: Processed ChIP-Seq data files are in wiggle format
|
|
|
Submission date |
Jun 29, 2017 |
Last update date |
May 15, 2019 |
Contact name |
James Bradner |
E-mail(s) |
[email protected]
|
Organization name |
Dana-Farber Cancer Institute
|
Department |
Medical Oncology
|
Lab |
Bradner Lab
|
Street address |
450 Brookline
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02215 |
Country |
USA |
|
|
Platform ID |
GPL11154 |
Series (2) |
GSE80151 |
Enhancer invasion shapes MYCN dependent transcriptional amplification in neuroblastoma [ChIP-seq] |
GSE80154 |
Enhancer invasion shapes MYCN dependent transcriptional amplification in neuroblastoma |
|
Relations |
BioSample |
SAMN07298762 |
SRA |
SRX2969262 |