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Sample GSM1333919 Query DataSets for GSM1333919
Status Public on Aug 05, 2014
Title RNA-seq wt 1
Sample type SRA
 
Source name Haemogenic Endothelium
Organism Mus musculus
Characteristics cell line: iDam
strain: 129
Growth protocol ES cell–derived haemogenic endothelium cells were routinely generated by isolating FLK1+ cells from d3.25 embryonic eody differentiations. FLK1+ cells where maintained on gelatin coated plates in liquid blast medium (IMDM supplemented with 10% FCS, P/S, 2mM L-Glutamine, 20μg/ml transferrin, 0.45mM MTG, 25μg/ml AA, 15% D4T conditioned medium, 5ng/ml VEGF and 10ng/ml IL6). After 2 days of liquid blast culture haemogenic endothelial cells where isolated according to the cKIT+ TIE2+ CD41- phenotype.
Extracted molecule total RNA
Extraction protocol RNA was isolated from snap frozen samples with the RNeasy Plus Mini Kit (Qiagen) and ribosomes depleted with the Ribozero Gold Kit (Epicentre) according to manufacturers instructions.
RNA-seq libraries were generated with the SOLiD Total RNA-Seq Kit (Life Technologies, 4445374).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model AB 5500xl Genetic Analyzer
 
Description FACS: cKIT+ TIE2+ CD41-
Data processing Sequencing reads were aligned to mm9 genome using SHRiMP2 with default settings. Reads aligning to multiple loci were discarded.
Reads were aligned to ENSEMBL (v66) annotated genes using the annmap database and Bioconductor package and only exonic reads were selected.
The Bioconductor package edgeR (FDR < 0.05; exact test method) was used to call differentially expressed genes between Runx1ko (iDamko, Ainv18ko ) and Runx1wt Bry-GFP or Runx1wt iDam HE samples
Common genes, which displayed same directional change, between the Runx1ko – Bry-GFP and Runx1ko – iDam comparisons were chosen for subsequent analysis
Genome_build: mm9
 
Submission date Feb 24, 2014
Last update date May 15, 2019
Contact name michael lie-a-ling
E-mail(s) Michael.Lie-A-Ling@ics.manchester.ac.uk
Organization name Cancer Research UK Manchester Institute
Department Stem Cell Biology
Street address The University of Manchester | Wilmslow Road
City manchester
ZIP/Postal code M204BX
Country United Kingdom
 
Platform ID GPL15907
Series (2)
GSE55310 RUNX1 positively regulates a cell adhesion and migration program in murine hemogenic endothelium prior to blood emergence (RNA-seq)
GSE55335 RUNX1 positively regulates a cell adhesion and migration program in murine hemogenic endothelium prior to blood emergence
Relations
Reanalyzed by GSE69080
BioSample SAMN02664687
SRA SRX475928

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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