NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM83453 Query DataSets for GSM83453
Status Public on Dec 01, 2005
Title NA11993, IVT: 1, Hyb: 2, SAM: 1221008, Array: B2
Sample type RNA
 
Source name lymphoblastoid cell line
Organism Homo sapiens
Characteristics HapMap CEU parent, Female
Biomaterial provider Coriell
http://locus.umdnj.edu/nigms/nigms_cgi/display.cgi?NA11993
Coriell
Growth protocol RPMI 1640 with Glutamax I medium (Invitrogen Corporation) supplemented with 10% fetal calf serum and 1% penicillin and streptomycin mix (Invitrogen Corporation). Cells lines were harvested at a density of 0.6 รป 1 x 10^6 cells/ml and at least 80 % viability. Cultures were spun for 5 min at 1000 g, and the resulting pellets were washed once in PBS and lysed by adding 2 ml of micro glass beads (Sigma) and vortexing in 1 ml lysis solution containing beta-mercaptoethanol (Qiagen, RNeasy kit). Cell lysates were stored at -80 oC.
Extracted molecule total RNA
Extraction protocol RNAs were extracted using RNeasy mini kits with on-column DNAse I digestion (Qiagen).
Label biotin
Label protocol One-quarter scale Message Amp II reactions (Ambion) were performed for each RNA extraction using 200 ng of total RNA. Biotin-16-UTP (Perkin Elmer) made up half of the UTP used in the in vitro transcription (IVT) reaction (37?C for 18 hours).
 
Hybridization protocol 1ug cRNA as per "Gene expression on Sentrix Arrays direct hybridization system manual" (Illumina Doc. #11161707, Rev. B) 2-21 2-32. Arrays were hybridized for 18 hours and stained with Cy3-Streptavidin.
Scan protocol Standard Illumina protocol, PMT 671 (factor 1.9573)
Description HapMap CEU parent
Data processing background-corrected values for each single bead type (raw data) were normalized on a log scale using a quantile normalization method (Bolstad et al. Bioinformatics, 2003. 19(2): p. 185-93)
 
Submission date Nov 15, 2005
Last update date Nov 16, 2005
Contact name Emmanouil T Dermitzakis
E-mail(s) emmanouil.dermitzakis@unige.ch
Phone +41 (0) 22 379 5483
Organization name University of Geneva Medical School
Department Department of Genetic Medicine and Development
Lab Population and comparative genomics
Street address 1 Rue Michel-Servet
City Geneva
ZIP/Postal code 1211
Country Switzerland
 
Platform ID GPL3090
Series (1)
GSE3612 HapMap CEU parent custom array expression

Data table header descriptions
ID_REF Probe name
raw probe data mean intensity for bead type (average ~30 beads)
raw background
VALUE log quantile normalised data

Data table
ID_REF raw probe data raw background VALUE
1998 347.5 198.6 8.545
2216 464.7 198.6 8.901
1317 187.9 198.6 7.731
1164 205 198.6 7.842
1170 209.5 198.6 7.872
2902 253.2 198.6 8.126
1042 449.2 198.6 8.85
6085 481.6 198.6 8.985
6004 218.6 198.6 7.93
781 210.3 198.6 7.877
1384 211.3 198.6 7.884
1685 194.9 198.6 7.776
3066 188.3 198.6 7.734
3780 201 198.6 7.814
4999 282.1 198.6 8.271
430 219.9 198.6 7.937
1009 207.8 198.6 7.858
1842 217.3 198.6 7.923
3706 203.1 198.6 7.829
4262 197.1 198.6 7.792

Total number of rows: 1433

Table truncated, full table size 31 Kbytes.




Supplementary data files not provided

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