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Sample GSM2586925 Query DataSets for GSM2586925
Status Public on Apr 24, 2017
Title 24hInd Control IgG ChIP (iSLK-Bac16WT cells)
Sample type SRA
 
Source name iSLK-Bac16WT cells
Organism Human gammaherpesvirus 8
Characteristics cell type: KSHV positive iSLK endothelial cells derived from gingival KS lesion
genotype/variation: RTA protein is under tet-inducible promoter
treatment: induced with doxycycline for 24h to trigger lytic reactivation
chip antibody: IgG (Cell Signaling Technology, catalog #2729, lot# 7)
Treatment protocol Cells were induced for lytic reactivation by Doxycycline for 24h.
Growth protocol iSLKBac16WT cells were grown in DMEM medium supplemented with 10%FBS 1ug/ml puromycin, 250 ug/ml G418, and 600 ug/ml hygromycin B
Extracted molecule genomic DNA
Extraction protocol Latent and lytic cells were cross-linked using formaldehyde to fix the protein-DNA for ChIP assay
Chromatins were immunoprecipitated using specific listed antibody by following standard ChIP protocol
ChIP DNA was used for library prepartation for ChIP-seq analysis
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model Illumina NextSeq 500
 
Description control IgG ChIP
Data processing The libraries were run on Illumina NextSeq500 instrument and Illumina software was used for peak calling
Sequenced reads were trimmed for adaptor sequence, and masked for low-complexity or low-quality sequence
Sequence were imported into CLC Genomic Workbech 10.0.1 with NCBI/Sanger or Illumia pipeline 1.8 and later option.
Reads were mapped to the KSHV genome database to determine the DNA bound by specific targets
ChIP peaks were calculated using CLC workbench ChiP-peak tool using input as reference
Genome_build: NCBI genome build of KSHV sequence accession# NC_009333
Supplementary_files_format_and_content: ChIP peaks on the viral genomes are in wig file (CLC workbench)
 
Submission date Apr 24, 2017
Last update date May 15, 2019
Contact name Subhash C Verma
E-mail(s) scverma@medicine.nevada.edu
Phone 775-682-6743
Organization name University of Nevada, Reno
Department Microbiology and Immunology
Lab Verma Lab
Street address 1664 N Virginia Street, MS 320
City Reno
State/province NV
ZIP/Postal code 89557
Country USA
 
Platform ID GPL23366
Series (2)
GSE98058 Identification of symmetric methylation of histone H4 arginine 3 on KSHV genome
GSE98087 Identification of symmetric methylation of histone H4 arginine 3 on KSHV genome (iSLKBac16WT ChIP-Seq)
Relations
BioSample SAMN06820782
SRA SRX2754559

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data not provided for this record

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