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Sample GSM1541552 Query DataSets for GSM1541552
Status Public on May 28, 2015
Title H3K9me3_sgSETDB1
Sample type SRA
 
Source name HeLa cells
Organism Homo sapiens
Characteristics cell line: HeLa
cell type: epithelial
disrupted gene: SETDB1
antibody: anti-H3K9me3 Abcam ab8898
Treatment protocol Transfected with pool of Cas9/sgRNA expression plasmids, and sorted for knockout cells that become GFP+ owing to de-repression of a silent GFP reporter construct
Growth protocol RPMI + 10% FCS + Penicillin/Streptomycin
Extracted molecule genomic DNA
Extraction protocol Crosslinking: 1% formaldehyde; Shearing: Bioruptor (Diagenode) to target size of 300bp; IP: 5ug primary antibody overnight
Illumina TruSeq ChIP Sample Prep Kit
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina HiSeq 2500
 
Data processing ChIP-seq reads were aligned to the reference human genome hg19 using Bowtie2 with default settings.
Data were imported into SeqMonk analysis software with minimum mapping quality of 20.
Genome was considered as a series of 1 kb 'windows' and the number of H3K9me3 ChIP-seq reads in each window quantitated for each sample, correcting for total read counts.
Windows containing low (H3K9me3 score <40) levels of H3K9me3 were filtered out.
Genome_build: hg19
Supplementary_files_format_and_content: Tab-delimited text file showing the H3K9me3 score for each cell type for each window.
 
Submission date Nov 07, 2014
Last update date May 15, 2019
Contact name Iva Tchasovnikarova
E-mail(s) it257@cam.ac.uk
Organization name University of Cambridge
Department The Gurdon Institute
Lab Tchasovnikarova Lab
Street address Tennis Court Road
City Cambridge
ZIP/Postal code CB2 1QN
Country United Kingdom
 
Platform ID GPL16791
Series (1)
GSE63116 H3K9me3 ChIP-seq in HeLa cells lacking TASOR, MPP8, periphilin and SETDB1
Relations
BioSample SAMN03169292
SRA SRX755642

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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