NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM92669 Query DataSets for GSM92669
Status Public on Jun 27, 2006
Title cRNA replicate hybridization 2
Sample type RNA
 
Channel 1
Source name Ovary_epithelium_cell_line
Organism Mus musculus
Characteristics in vitro amplified cRNA, replica2
Extracted molecule total RNA
Label Cy3
Label protocol Indirect labeling during in vitro amplification
 
Channel 2
Source name Ovary_epithelial_cell_line
Organism Mus musculus
Characteristics in vitro amplified cRNA, replica 1
Extracted molecule total RNA
Label Cy5
Label protocol Indirect labeling during in vitro amplification
 
 
Hybridization protocol See Livesey, F. J., Furukawa, T., Steffen, M. A., Church, G. M. and Cepko, C. L. (2000). Microarray analysis of the transcriptional network controlled by the photoreceptor homeobox gene Crx. Curr Biol 10, 301-10
Scan protocol Hybridised microarrays were scanned on a GenePix 4000B microarray scanner and the resulting images were analysed with GenePix 5 array analysis software
Description RNA was extracted by the Invitrogen Trizol Protocol, Ref: Chomczynski, P. and Sacchi, N. (1987) Analytical Biochemistry 162, 156. 10 ug of total RNA was amplified in 3 rounds of T7-based amplification MessageAmpII aRNA Kit, Ambion) in two parallel reacxtions. cRNA replica2 and 1 were indirectly labeled with Cy3 and with Cy5 correspondently, following by co-hybridisation on the slide
Data processing Limma packadge: log-ratio were lowess normalized, filtered to exclude spots flagged as bad and backgroud corrected.
 
Submission date Jan 17, 2006
Last update date Jun 27, 2006
Contact name Tatiana Subkhankulova
E-mail(s) subkhankul@hotmail.com
Phone 02075941825
Organization name Queen Mary University London
Department Neuroscience
Lab Silvia Marino
Street address 4 Newark Street
City London
ZIP/Postal code E1 2AD
Country United Kingdom
 
Platform ID GPL2584
Series (1)
GSE5136 Comparison of linear and exponential amplification techniques for expression profiling at the single-cell level

Data table header descriptions
ID_REF
VALUE cRNA_replica2_vs_cRNA_replica1

Data table
ID_REF VALUE
CG_Mm_3000205_1 null
CG_Mm_3000208_1 -0.828760357081479
CG_Mm_3000211_1 -0.0580606066018055
CG_Mm_3000214_1 0.0587767277924049
CG_Mm_3000229_1 null
CG_Mm_3000232_1 null
CG_Mm_3000235_1 0.125048291836589
CG_Mm_3000238_1 -0.344354644972039
CG_Mm_3000253_1 null
CG_Mm_3000256_1 -0.661770450105971
CG_Mm_3000259_1 null
CG_Mm_3000262_1 -0.307002986207259
CG_Mm_3000277_1 -0.490829005012213
CG_Mm_3000280_1 -0.248885722116832
CG_Mm_3000283_1 -0.386635557851144
CG_Mm_3000286_1 null
CG_Mm_3000589_1 0.255859873274611
CG_Mm_3000592_1 -0.227239329843762
CG_Mm_3000595_1 -0.0585282378463889
CG_Mm_3000598_1 -0.254332970108365

Total number of rows: 21997

Table truncated, full table size 616 Kbytes.




Supplementary data files not provided

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap