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Sample GSM869413 Query DataSets for GSM869413
Status Public on Apr 02, 2012
Title Runx-rep1
Sample type RNA
 
Source name myoblasts transduced with lentivirus carrying Runx1
Organism Homo sapiens
Characteristics cell line: RD cells
Treatment protocol RD cells were infected with titer-matched amounts of either RUNX1-, ZNF238-, miR-206- or GFP-expressing lentiviruses, allowed to recover in growth media for 24 hours, and then shifted to differentiation media for 72 hours. Each condition was performed with 3 independent biological replicates.
Growth protocol RD cells were obtained from ATCC (American Type Culture Collection) in approximately 1990, and all analyses have been performed on cells that originated from low passage number frozen aliquots. Cells were maintained in DMEM with 10% bovine calf serum and 1% Pen-Strep (Gibco). Low-serum differentiation media consisted of DMEM with 1% horse serum, 1% Pen-Strep and 10 ug/mL insulin and transferrin.
Extracted molecule total RNA
Extraction protocol RNA was extracted with Qiagen RNeasy kit according to manufacturer's instruction. Quality control was performed with Agilent Bioanalyzer.
Label biotin
Label protocol Biotinylated cRNA were prepared with the Illumina TotalPrep RNA Amplification Kit (Applied Biosystems) for Illumina arrays
 
Hybridization protocol Standard Illumina hybridization protocol
Scan protocol Standard Illumina scanning protocol
Data processing Probe intensities were corrected, normalized, and summarized by the Lumi package of Bioconductor (Du et al., 2008). Differentially expressed genes were identified by the LIMMA package of Bioconductor (Wettenhall and Smyth, 2004).
Data was vst transformed and quantile normalized using the Lumi package of Bioconductor (Du et al., 2008).
 
Submission date Feb 01, 2012
Last update date May 17, 2012
Contact name Janet M. Young
E-mail(s) jayoung@fhcrc.org
Phone 206 667 1471
Organization name Fred Hutchinson Cancer Research Center
Department Division of Human Biology
Lab Tapscott
Street address 1100 Fairview Avenue N., C3-168, P.O. Box 19024
City Seattle
State/province WA
ZIP/Postal code 98109
Country USA
 
Platform ID GPL10558
Series (2)
GSE35491 miR-206 integrates multiple components of differentiation pathways to control the transition from growth to differentiation in rhabdomyosarcoma cells (Illumina)
GSE35921 miR-206 integrates multiple components of differentiation pathways to control the transition from growth to differentiation in rhabdomyosarcoma cells

Data table header descriptions
ID_REF
VALUE vst transformed, quantile normalized signal intensity
Detection Pval

Data table
ID_REF VALUE Detection Pval
ILMN_1762337 5.705283376 0.48442
ILMN_2055271 6.315659517 0.02078
ILMN_1736007 5.555053994 0.74416
ILMN_2383229 5.70077917 0.49481
ILMN_1806310 6.281559861 0.02597
ILMN_1779670 5.937532895 0.20649
ILMN_1653355 5.921109304 0.21429
ILMN_1717783 5.522809708 0.8013
ILMN_1705025 5.812981397 0.33636
ILMN_1814316 8.464880821 0
ILMN_2359168 8.571872911 0
ILMN_1731507 6.761495037 0.0026
ILMN_1787689 6.06483568 0.1013
ILMN_3241953 5.797039253 0.36104
ILMN_1745607 7.729067173 0
ILMN_2136495 5.537133905 0.77922
ILMN_1668111 5.418273278 0.91169
ILMN_2295559 5.92358977 0.21169
ILMN_1735045 6.93266218 0.0013
ILMN_1680754 5.901672773 0.23117

Total number of rows: 47323

Table truncated, full table size 1452 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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