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Sample GSM2043050 Query DataSets for GSM2043050
Status Public on Feb 25, 2017
Title wt deleted cells
Sample type SRA
 
Source name wt deleted cells
Organism Schizosaccharomyces pombe
Characteristics growth stage: log growing cells
genotype/variation: Wild type
Treatment protocol Genomic deletion of ago1d, mmi1, and dcr1.
Growth protocol Standard conditions were used to produce logarithmically growing cultures in rich media (YEA). Cultures were grown at 30C.
Extracted molecule total RNA
Extraction protocol RNA was extracted using the MasterPureā„¢ Yeast RNA Purification Kit (epicentre)
ScriptSeq v2 RNA-Seq Library Preparation Kit was used according to manufacturer's recommendation.
Libraries were analyzed using an Agilent 2100 BioAnalyzer (Agilent) and sequenced on the Illumina MiSeq platform.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina MiSeq
 
Data processing Alignment was done using Tophat.
FPKM values were calculated using cufflinks
Genome_build: asm294v2.28
Supplementary_files_format_and_content: Tab delimited text files, from cufflinks
 
Submission date Jan 20, 2016
Last update date May 15, 2019
Contact name Shiv Grewal
Phone 2407607553
Organization name NCI
Department LBMB
Lab Shiv Grewal
Street address NCI bldg 37 Rm 6068 9000 Rockville Pike
City Bethesda
State/province MD
ZIP/Postal code 20892
Country USA
 
Platform ID GPL16192
Series (2)
GSE77047 Untimely expression of gametogenic genes in vegetative cells causes uniparental disomy (RNA-seq)
GSE77050 Untimely expression of gametogenic genes in vegetative cells causes uniparental disomy
Relations
BioSample SAMN04431485
SRA SRX1539180

Supplementary file Size Download File type/resource
GSM2043050_spr156.fpkm_tracking.gz 205.4 Kb (ftp)(http) FPKM_TRACKING
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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