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Sample GSM2229418 Query DataSets for GSM2229418
Status Public on Jun 30, 2017
Title RNA-seq_MutuI+Ab+JQ1_Replicate2
Sample type SRA
 
Source name MutuI (EBV+ Burkitt lymphoma cell line)
Organisms Homo sapiens; human gammaherpesvirus 4
Characteristics pathogen: Epstein-Barr virus
cell line: mutuI
1h pretreatment: JQ1
1 day treatment: antibody
Treatment protocol Log phase cultures were pretreated for 1 hour with 1 μM JQ1 (EMD Millipore) or vehicle, then treated for 1 day with 10 μg/mL goat anti-human IgG, IgM, IgA secondary antibody (Thermo Scientific, PI31128) or vehicle
Growth protocol MutuI cells were maintained in RPMI-1640 with 25 mM HEPES and 2 g/L NaHCO3 in 5% CO2 with 10% (v/v) fetal bovine serum (Invitrogen)
Extracted molecule total RNA
Extraction protocol RNA was extracted and cDNA was prepared as described in the paper
RNA-seq libraries were prepared as described in the paper
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Description Sample name: 69
Data processing 50 bp reads were mapped using Bowtie to an index containing both the human hg19 and EBV reference [GenBank ID: NC_007605.1] genomes.
Parameters allowed for up to two mismatches and only considered reads that mapped to a unique sequence.
Wigs: The number of hits at each base was counted and then normalized per million mapped reads.
Wigs: Formatted for uploading to Integrative Genomics Viewer (www.broadinstitute.org/igv/)
Spreadsheet: Differential expression of human genes 28 upon drug treatment was calculated by comparing independent triplicate experiments where MutuI cells were treated with 1 μM JQ1 or vehicle for 1 day.
Spreadsheet: Adaptors and low-quality portions of reads were trimmed with Fastq-mcf, sequence quality control assessed with FastQC and RSeQC, and spliced and unspliced reads aligned to the hg19 reference human genome with Tophat 2.0.13 and Bowtie 2.2.4, respectively.
Spreadsheet: Reads were assigned to genes as annotated by Ensembl using featureCounts. Genes yielding counts per million expression below 0.5 or above 5000 in more than one sample were excluded for analysis.
Spreadsheet: Re-normalization of all other genes and calculation of differential expression p-values were performed with edgeR. The false discovery rate for each p-value was calculated using the Benjamini-Hochberg method with R. Pathway enrichment analysis was performed with GO-Elite 1.2.5 and a cut-off p-value of 0.05.
Genome_build: Index contains both the human hg19 and EBV [GenBank ID: NC_007605.1] reference genomes
Supplementary_files_format_and_content: Wigs are formatted for IGV. Genome file chrEBV(B95_8_Raji).fa is available from http://www.flemingtonlab.com/rnaseq.html. Wig columns are chromosome, start, stop, counts per million mapped reads.
 
Submission date Jul 10, 2016
Last update date May 15, 2019
Contact name JJ Miranda
E-mail(s) jmiranda@barnard.edu
Organization name Barnard College, Columbia University
Street address 3009 Broadway
City New York
ZIP/Postal code 10027
Country USA
 
Platform ID GPL22131
Series (2)
GSE84209 BET inhibitors suppress BZLF1 expression [MutuI RNA-seq]
GSE84214 BET inhibitors block the Epstein-Barr virus lytic cycle at two distinct steps
Relations
BioSample SAMN05370900
SRA SRX1923413

Supplementary file Size Download File type/resource
GSM2229418_KMK_69-m1.maphv.grep.xy.xyn.igv.wig.gz 985.6 Kb (ftp)(http) WIG
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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