NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2113526 Query DataSets for GSM2113526
Status Public on Jan 29, 2018
Title KELLY_MYCN
Sample type SRA
 
Source name KELLY_Neuroblastoma
Organism Homo sapiens
Characteristics cell line: KELLY
cell type: neuroblastoma cell line
growth condition: 10% FBS, DMEM
treated with: None
chip antibody: MYCN
chip antibody vendor: abcam
chip antibody cat. #: ab16898
input: KELLY_INPUT
barcode: TTCCATTG
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 NextSeq 500
 
Description Chromatin IP against MYCN in KELLY
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 Apr 11, 2016
Last update date May 15, 2019
Contact name James Bradner
E-mail(s) bradner_computation@dfci.harvard.edu
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 GPL18573
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 SAMN04632501
SRA SRX1690210

Supplementary file Size Download File type/resource
GSM2113526_KELLY_MYCN.wig.gz 104.7 Mb (ftp)(http) WIG
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap