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Sample GSM159574 Query DataSets for GSM159574
Status Public on Feb 09, 2007
Title NA18524
Sample type RNA
 
Source name lymphoblastoid cell line
Organism Homo sapiens
Characteristics HapMap CHB, Male
Biomaterial provider Coriell http://ccr.coriell.org/Sections/Search/Search.aspx?PgId=165&q=NA18524
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 ~ 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°C.
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 Celsius for 18 hours).
 
Hybridization protocol 1.5ug cRNA as as per Gene expression on Sentrix® Arrays direct hybridization system manual (Illumina Doc. #11161707, Rev. B). Arrays were hybridized for 18 hours and stained with Cy3-Streptavidin.
Scan protocol Standard Illumina protocol, PMT 638
Description HapMap CHB Male
Data processing background-corrected values for each single bead type (raw data) were normalised on a log scale using a quantile normalization method (Bolstad et al. Bioinformatics, 2003. 19(2): p. 185-93) across replicates of a single individual, followed by a median normalisation across individuals of a single population.
 
Submission date Jan 31, 2007
Last update date Oct 01, 2007
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 GPL2507
Series (1)
GSE6536 Whole-genome gene expression variation in 210 unrelated HapMap individuals

Data table header descriptions
ID_REF
VALUE log quantile + median normalised data

Data table
ID_REF VALUE
GI_10047089-S 5.801267
GI_10047091-S 6.577994
GI_10047093-S 9.703362
GI_10047099-S 8.077599
GI_10047103-S 11.974305
GI_10047105-S 6.368728
GI_10047121-S 5.727790
GI_10047123-S 9.656727
GI_10047133-A 5.837037
GI_10047133-I 6.306672
GI_10092578-S 6.063478
GI_10092585-S 7.309929
GI_10092596-S 7.147480
GI_10092600-S 9.489656
GI_10092602-S 5.902319
GI_10092603-S 5.885757
GI_10092611-A 8.927377
GI_10092616-S 6.678780
GI_10092618-S 13.780066
GI_10092638-S 6.356384

Total number of rows: 47293

Table truncated, full table size 1010 Kbytes.




Supplementary file Size Download File type/resource
GSM159574_NA18524_1_1.txt.gz 247.0 Kb (ftp)(http) TXT
GSM159574_NA18524_1_2.txt.gz 248.6 Kb (ftp)(http) TXT
GSM159574_NA18524_2_1.txt.gz 251.7 Kb (ftp)(http) TXT
GSM159574_NA18524_2_2.txt.gz 253.8 Kb (ftp)(http) TXT
Processed data included within Sample table

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