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Sample GSM4146247 Query DataSets for GSM4146247
Status Public on Dec 03, 2019
Title hKRT_Mi2KD_cJUN_ChIP_rep1
Sample type SRA
 
Source name neonatal foreskin
Organism Homo sapiens
Characteristics cell types: keratinocytes
genotype: Mi2KD
Extracted molecule genomic DNA
Extraction protocol Primary human epidermal keratinocytes were incubated for 6 hours with the infection medium containing lentiviral particles derived from shRNA lentiviral constructs for Mi-2β or control, and then selected for 3-5 days in puromycin.
As detailed in Hu et al. Genes Dev (2016)
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina HiSeq 2000
 
Data processing Basecalls were performed using bcl2fastq v. 1.8.3
Read alignment was performed on the mm10 (mouse genome) or hg19 (human genome) assembly using the genome mappers Bowtie2 for ATACseq and STAR for RNAseq and ChIPseq.
For RNA-seq, read normalization, RPKM and differential gene expression, were performed using the HOMER scripts analyzeRepeats.pl and getDiffExpression.pl with implementation of DESeq2 through R.
Peak calling for ATAC-seq was perfomed using MACS2 call peaks with --keep-dup all --nomodel --shift 37 --extsize 73.
Peak calling for ChIP-seq was performed using the Homer findPeaks algorithm.
Genome_build: mm10, hg19
 
Submission date Oct 31, 2019
Last update date Dec 03, 2019
Contact name Katia Georgopoulos
E-mail(s) [email protected]
Phone 617-7264445
Organization name Harvard Medical School
Department CBRC
Lab Georgopoulos
Street address 1st and 13th St
City Charlestown
State/province MA
ZIP/Postal code 02129
Country USA
 
Platform ID GPL11154
Series (1)
GSE139685 Functional interactions between Mi-2β and AP1 complexes control response and recovery from barrier disruption
Relations
BioSample SAMN13173327
SRA SRX7082276

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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