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Sample GSM417716 Query DataSets for GSM417716
Status Public on Sep 13, 2009
Title Control-KD mRNA-Seq
Sample type SRA
 
Source name 293T cells
Organism Homo sapiens
Characteristics cell l ine: 293T
Treatment protocol Day 0: plate cells in 10cm dishes. Day 1: transfect 20nM siRNA using Dharmafect 1 (Dharmacon) as transfection reagent. Day 2: transfect 50nM siRNA using Dharmafect 1 (Dharmacon) as transfection reagent. Day 4: harvest cells. Transfections were conducted using protocols suggested by the manufacturer of the transfection reagent.
Growth protocol 293T cells were cultured with D-MEM medium supplemented with 10% fetal bovine serum.
Extracted molecule polyA RNA
Extraction protocol mRNA is purified from total RNA with oligo-dT magnetic beads. cDNA is synthesized with random primer priming. ds-cDNA is sequenced using Illumina Genome Analyzers as recommended by the manufacturer.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina Genome Analyzer
 
Description n/a
Data processing short reads mapping to human genome hg18 using Eland
 
Submission date Jun 16, 2009
Last update date May 15, 2019
Contact name Xinshu Xiao
E-mail(s) gxxiao@ucla.edu
Organization name MIT
Department Biology
Lab Chris Burge Lab
Street address 77 Mass Ave. MIT, 68-211
City Cambridge
State/province MA
ZIP/Postal code 02139
Country USA
 
Platform ID GPL9052
Series (1)
GSE16642 Illumina mRNA-Seq of control and hnRNP H knockdown in 293T cells
Relations
SRA SRX012335
BioSample SAMN00004611

Supplementary file Size Download File type/resource
GSM417716_ctrl_realign.txt.gz 495.4 Mb (ftp)(http) TXT
SRA Run SelectorHelp
Processed data provided as supplementary file
Raw data are available in SRA

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