|
| Status |
Public on Aug 06, 2007 |
| Title |
HBP ALL day 3 1uM MRK-003 |
| Sample type |
RNA |
| |
|
| Channel 1 |
| Source name |
HBP ALL day 3 DMSO
|
| Organism |
Homo sapiens |
| Characteristics |
T-ALL cell line
|
| Treatment protocol |
T-ALL cell lines were plated at a density of 5e4-1.5e5 cells per ml (depending on doubling time) and were treated with 1uM MRK-003 for 3 days.
|
| Growth protocol |
T-ALL cell lines were plated at a density of 5e4-1.5e5 cells per ml (depending on doubling time) and were treated with 1uM MRK-003 for 3 days.
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Qiagen RNeasy spin columns with DNAse treatment
|
| Label |
Cy3
|
| Label protocol |
custom automated version of the aminoallyl MessageAmp II kit from Ambion.
|
| |
|
| Channel 2 |
| Source name |
HBP ALL day 3 1uM MRK-003
|
| Organism |
Homo sapiens |
| Characteristics |
T-ALL cell line
|
| Treatment protocol |
T-ALL cell lines were plated at a density of 5e4-1.5e5 cells per ml (depending on doubling time) and were treated with 1uM MRK-003 for 3 days.
|
| Growth protocol |
T-ALL cell lines were plated at a density of 5e4-1.5e5 cells per ml (depending on doubling time) and were treated with 1uM MRK-003 for 3 days.
|
| Extracted molecule |
total RNA |
| Extraction protocol |
Qiagen RNeasy spin columns with DNAse treatment
|
| Label |
Cy5
|
| Label protocol |
custom automated version of the aminoallyl MessageAmp II kit from Ambion.
|
| |
|
| |
| Hybridization protocol |
Microarrays are incubated at 40°C for 48 hours in a rotating carousel. Hybridizations to custom Agilent microarrays are completed as previously described (Hughes et al.Nat Biotech (2001), 19(4):342-7). Microarrays are washed to remove non-specific hybridized sample. Afterwards, microarrays are dried in an ozone-free nitrogen chamber.
|
| Scan protocol |
Microarrays are scanned using the Agilent LP2 laser scanner. The scanner output is a Tiff file, which contains the quantitative hybridization data from each individual microarray. The Tiff files are then processed using Rosetta custom feature extraction software.
|
| Description |
T-ALL cell line
|
| Data processing |
Data were processed using the Rosetta Resolver® system. Rosetta's custom feature extraction software performs error modeling before data are loaded into the Resolver system. The Resolver system performs a squeeze operation that combines replicates of the same sequence in an array while applying error weighting. The error weighting consists of adjusting for additive and multiplicative noise. A P-value is generated and propagated throughout the system. The P-value represents the probability that a gene is expressed. The Resolver system allows users to set thresholds, below which genes of a P-value are considered to be significantly expressed. The Resolver system also combines multiple arrays using a squeezing process. If multiple spots reference one sequence, summarization is performed using an error-weighted average as described in Roland Stoughton and Hongyue Dai, Statistical Combining of Cell Expression Profiles. US Patent #6,351,712, February 26, 2002.
|
| |
|
| Submission date |
Jul 06, 2007 |
| Last update date |
Aug 14, 2011 |
| Contact name |
Olivia Fong |
| E-mail(s) |
olivia.fong@merck.com
|
| Organization name |
Merck & Co.
|
| Department |
Molecular Profiling
|
| Lab |
Merck Research Laboratories
|
| Street address |
P.O. Box 2000
|
| City |
Rahway |
| State/province |
NJ |
| ZIP/Postal code |
07065 |
| Country |
USA |
| |
|
| Platform ID |
GPL4372 |
| Series (1) |
|
