|
Status |
Public on Apr 01, 2013 |
Title |
Prdm14 knockout 1 |
Sample type |
RNA |
|
|
Source name |
embryonic stem cell
|
Organism |
Mus musculus |
Characteristics |
cell type: embryonic stem cell genetic background: C57BL/6 genotype: Prdm14 knockout
|
Treatment protocol |
Biological replicates were collected from consecutive passages, no additional treatment was performed.
|
Growth protocol |
Prdm14-null and wild-type control cells were grown in 2i culture conditions as described by Ying et al. (Nature, 2008)
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was extracted with the RNeasy kit from Qiagen, followed by clean-up and DNase I treatment in accordance with the prescribed protocol provided with the kit. Quality control was performed with Agilent Bioanalyser.
|
Label |
biotin
|
Label protocol |
The Illumina Total-prep 96-RNA amplification kit from Ambion was used.
|
|
|
Hybridization protocol |
Standard Illumina hybridization protocol
|
Scan protocol |
Standard Illumina scanning protocol
|
Data processing |
The data were normalised using quantile normalisation with the lumi package in Bioconductor not detected probes omitted (detection p-value where a probe is not detected in a sample if the p-value is above 0.01)
|
|
|
Submission date |
Mar 26, 2013 |
Last update date |
Apr 01, 2013 |
Contact name |
Charles Bradshaw |
Organization name |
University of Cambridge
|
Department |
Gurdon Institute
|
Street address |
Tennis Court Road
|
City |
Cambridge |
ZIP/Postal code |
CB2 1QN |
Country |
United Kingdom |
|
|
Platform ID |
GPL6887 |
Series (2) |
GSE45507 |
Genome-wide identification of genes differentially expressed between wild-type and Prdm14-deficient ES cells grown in 2i culture conditions. |
GSE45509 |
Prdm14 |
|