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Sample GSM2628285 Query DataSets for GSM2628285
Status Public on May 09, 2018
Title input_2
Sample type SRA
 
Source name input
Organism Nicotiana tabacum
Characteristics tissue: BY2 lysate (BYL)
cultivar: bright yellow 2 (BY2)
Growth protocol Nicotiana tabacum BY2 cells were grown in Murashige-Skoog liquid medium at 23°C.
Extracted molecule total RNA
Extraction protocol Evacuolated BY2 protoplasts were obtained by percoll gradient centrifugation and extracts were prepared from cells disrupted by a dounce homogenizer. Small RNAs were precipitated by the p19 siRNA binding protein.
RNA libraries were prepared using illumina protocolls.
 
Library strategy miRNA-Seq
Library source transcriptomic
Library selection size fractionation
Instrument model Illumina HiScanSQ
 
Data processing adapter trimming by cutadapt
quality filtering by sickle -q 20 -l 15
maping by bowtie-1.1.2 to rRNA.fa
mapping of unmapped reads by bowtie-1.1.2 to HAIRPIN_SNORNA.fa
counting of mapped reads by Rsamtools
testing for differenial expression and normalisation by edgeR
Genome_build: miRBase v21
Supplementary_files_format_and_content: tab-delimited text files include raw counts and tmm normalized counts for each Sample.
 
Submission date May 16, 2017
Last update date May 15, 2019
Contact name Claus Weinholdt
E-mail(s) claus.weinholdt@informatik.uni-halle.de
Organization name Martin Luther University Halle-Wittenberg
Department Institute of Computer Science
Street address Von-Seckendorff-Platz 1
City Halle
ZIP/Postal code 06120
Country Germany
 
Platform ID GPL23484
Series (1)
GSE98956 RNA sequencing of plant microRNAs precipitated by the tombusviral suppressor of RNA silencing p19.
Relations
BioSample SAMN07127090
SRA SRX2828635

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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