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Status |
Public on Feb 09, 2007 |
Title |
NA18558 |
Sample type |
RNA |
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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=NA18558
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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).
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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.
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Submission date |
Jan 31, 2007 |
Last update date |
Oct 01, 2007 |
Contact name |
Emmanouil T Dermitzakis |
E-mail(s) |
[email protected]
|
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 |
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