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Sample GSM1503906 Query DataSets for GSM1503906
Status Public on Dec 01, 2014
Title siUPF1+siXRN1 Bio1 RNA-seq
Sample type SRA
 
Source name HeLa+TCRβ68
Organism Homo sapiens
Characteristics cell line: HeLa
stably transfected reporter: TCRβ68
transient transfection: siUPF1 and siXRN1
Treatment protocol transfected with siRNAs targeting UPF1 and XRN1
Extracted molecule polyA RNA
Extraction protocol RNAseq libraries were constructed from poly(A)+ RNA using TruSeq RNA sample prep kit (Illumina)
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Description RNA-Seq libraries from HeLa cells stably transfected with TCRβ68 and transiently transfected with siRNAs targeting siUPF1 and siXRN1
Processed data file: isoform_expression.txt
Data processing [All] base calling was done using bcl2fastq_1.8.3
[RNA-Seq] Sequenced reads were trimmed for adapter sequence and mapped to hg19 whole genome using Tophat v2.0.11, with 1 mismatch, gtf file gencode.v11.annotation.gtf, --no-novel-juncs
[RNA-Seq] Transcript abundance (fpkm) was calculated using Cufflinks V2.2.0 using compatible hits normalization
[PARE, SPARE, C-PARE] Sequenced reads were trimmed for adapter sequence and raw abundance was counted
Genome_build: hg19
Supplementary_files_format_and_content: Transcript abundance (fpkm) reported for RNA-Seq samples. Trimmed sequence and sequence abundance reported for PARE, SPARE, C-PARE samples.
 
Submission date Sep 13, 2014
Last update date May 15, 2019
Contact name Pamela J Green
Organization name University of Delaware
Department Delaware Biotechnology Institute
Street address 15 Innovation Way
City Newark
State/province DE
ZIP/Postal code 19711
Country USA
 
Platform ID GPL16791
Series (1)
GSE61398 Direct identification of endogenous SMG6 targets and a preferred motif spanning SMG6 cleavage sites by parallel analysis of RNA ends in human cells
Relations
BioSample SAMN03067840
SRA SRX700558

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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