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Sample GSM3123061 Query DataSets for GSM3123061
Status Public on May 02, 2018
Title shDDX1_rep1
Sample type SRA
 
Source name INS-1_shDDX1
Organism Rattus norvegicus
Characteristics cell line: INS1
cell type: pancreatic beta cell line
shRNA: DDX1
Extracted molecule total RNA
Extraction protocol Total RNA was prepared directly from the scrambled and shDDX1 INS1 cells using Trizol (Invitrogen, Carlsbad, CA, USA) as per the manufacturer's instructions.
The mRNA was purified by Dynabeads mRNA DIRECT kit (Invitrogen, Carlsbad, CA, USA) from total RNA, fragmented, converted to cDNA.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Data processing Trimmomatic v0.36 was used to trim/filter sequenced reads with default parameters
Sequencing reads were mapped to the rat genome (version Rn5) using Tophat (version 2.0.9) and the default options(Kim et al., 2013). Mapped reads were used with Cufflinks software suite (Trapnell et al., 2012) in combination with rat transcripts annotations from Ensembl database(Aken et al., 2016) version 79 for transcripts assembly.
Genome_build: rn5
Supplementary_files_format_and_content: bigwig files were generated using UCSC bedGraphToBigWig
 
Submission date May 01, 2018
Last update date May 03, 2018
Contact name Wen Zhong
E-mail(s) zhongwenhust@gmail.com
Organization name Institute of Biophysics, Chinese Academy of Sciences
Street address Datun Road
City Beijing
ZIP/Postal code 100101
Country China
 
Platform ID GPL18694
Series (1)
GSE113893 DDX1 regulates alternative splicing and insulin secretion in pancreatic β cells
Relations
BioSample SAMN09006373
SRA SRX4016837

Supplementary file Size Download File type/resource
GSM3123061_shDDX1_rep1.bw 216.7 Mb (ftp)(http) BW
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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