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Sample GSM506667 Query DataSets for GSM506667
Status Public on Apr 09, 2010
Title FC112_L6_M3_CCC
Sample type SRA
 
Source name TuMV
Organisms Arabidopsis thaliana; Turnip mosaic virus
Characteristics time point: 10 dpi
genotype: Col-0
Treatment protocol Plants were inoculated with enriched TuMV virion preparations or with buffer (mock).
Growth protocol Plants were grown in a greenhouse with a 16-hr light/8-hr dark cycle.
Extracted molecule total RNA
Extraction protocol Small RNAs were separated from total RNA by size fractionation and converted to DNA amplicons by serial adaptor ligation to both ends followed by RT-PCR. DNA amplicons were sequenced using an Ilumina Genome Analyzer.
5' adaptor GUUCAGAGUUCUACAGUCCGACGAUC and 3' adaptor CTGTAGGCACCATCAAT
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection size fractionation
Instrument model Illumina Genome Analyzer
 
Description Single plant
Data processing Small RNA sequences were parsed from Illumina sequencing data files through identification of the 3' adaptor boundary and the 5' barcode. Only sequences that mapped perfectly to Arabidopsis thaliana or to TuMV genomes were included in the analysis.
 
Submission date Feb 04, 2010
Last update date Jun 11, 2013
Contact name James C Carrington
E-mail(s) jcarrington@danforthcenter.org
Phone 314-587-1202
Organization name Donald Danforth Plant Science Center
Lab James C. Carrington
Street address 975 North Warson Road
City Saint Louis
State/province MO
ZIP/Postal code 63132
Country USA
 
Platform ID GPL10065
Series (1)
GSE20197 Accumulation of TuMV-derived siRNAs in aerial parts of Arabidopsis thaliana plants at 7 and 10 dpi
Relations
BioSample SAMN02196485

Supplementary file Size Download File type/resource
GSM506667_Carrington_At_160.txt.gz 1.5 Mb (ftp)(http) TXT
GSM506667_Carrington_TuMV_48.txt.gz 138.0 Kb (ftp)(http) TXT
Processed data provided as supplementary file

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