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Status |
Public on Dec 16, 2015 |
Title |
RNA-seq in LCL, EBNA1 shRNA, replicate 1 |
Sample type |
SRA |
|
|
Source name |
LCL_EBNA1 shRNA_RNA-seq
|
Organism |
Homo sapiens |
Characteristics |
cell line: LCL cell type: EBV positive B-cell transduced with: shEBNA1 lentivirus
|
Treatment protocol |
LCL cells transduced with either pLKO.1 shControl or shEBNA1 lentivirus after 5 days of puromycin selection Cells were maintained and isolated in logarihmic growth phase for ChIP-assays. RNA Seq analysis was performed with LCL cells transduced with either pLKO.1 shControl or shEBNA1 lentivirus after 5 days of puromycin selection.
|
Growth protocol |
EBV positive B-cell (Raji, Mutu I, LCL) were grown in RPMI with 10% FBS and Glutamax. EBV positive NPC-line C666-1 was grown in DMEM with 10% FBS and Glutamax.
|
Extracted molecule |
total RNA |
Extraction protocol |
total RNA isolated using Trizol reagent TruSeq Stranded Total RNA Library Preparation kit ChIP-Seq protocol is as described previously (Lu et al, 2010 Virology journal 7, 262). Total RNA was isolated for RNA-Seq using Trizol reagent.
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|
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
|
|
Description |
RNA.LCL.shEBNA1.1
|
Data processing |
All chip-seq files were generated by Illumina GA II and base calling was done with CASAVA 1.5 Chip-seq files were aligned using bowtie version 0.12.9 to human genome hg19 Peak calling was done with homer (v1.0) software with -center -o, -fdr 0.2 RNA-Seq data analyzing was done with rsem(ver. 1.2.3) and Hg19 genome with UCSC known gene set. edgeR was used for differentail expression analysis Genome_build: hg19 Supplementary_files_format_and_content: Prosessed files contains Homer peak calling output while expression file contains the edgeR output; details in the 'readme.txt'
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Submission date |
Oct 09, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Priyankara J Wickramasinghe |
E-mail(s) |
[email protected]
|
Phone |
2154956837
|
Organization name |
The Wistar Institute
|
Department |
Bioinformatics
|
Lab |
Genomics
|
Street address |
3601 Spruce Street
|
City |
Philadelphia |
State/province |
PA |
ZIP/Postal code |
19104 |
Country |
USA |
|
|
Platform ID |
GPL16791 |
Series (1) |
GSE73887 |
Identification of MEF2B, EBF1, and IL6R as chromosome bound targets of EBNA1 essential for EBV infected B-lymphocyte survival |
|
Relations |
BioSample |
SAMN04158416 |
SRA |
SRX1322307 |