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Sample GSM522855 Query DataSets for GSM522855
Status Public on Feb 02, 2011
Title 516123_F2_167
Sample type RNA
 
Source name 516123_F2_167
Organism Mus musculus
Characteristics strain: B6/J x A/J
tissue: liver
Extracted molecule total RNA
Extraction protocol Samples are processed in parallel in 96-well plates to minimize potential variation. Reaction purification is achieved using magnetic binding beads for cDNA and Qiagen RNeasy kits for cRNA purification.
Label Biotin is incorporated during the amplification. This binds a streptavidin-conjugated phycoerythrin during the post-hybridization staining process that provides the measurable signal.
Label protocol The final in vitro transcription incorporates biotin moieties that are later labeled with phycoerythrin. After amplification, samples are put through a controlled fragmentation to improve hybridization sensitivity and consistency. The labeled molecules are biotinylated-cRNA.
 
Hybridization protocol GeneChip microarrays are loaded with the fragmented target sample/hybridization buffer mix using standard manual techniques. Arrays are hybridized for 18 hours at 45?C with vigorous mixing. Unbound sample is removed and staining is accomplished through the binding of streptavidin conjugated phycoerythrin to the hybridized target. Excess label is removed. Washing and staining steps are performed by the Affymetrix FS450 fluidics station using standard protocols.
Scan protocol Arrays are scanned using a GeneChip Scanner 3000 7G with a 48 array autoloader. The scanner maintains the optimal temperature for the arrays prior to and during scanning.
Description Affymetrix Mouse liver gene expression profiling of Cross B6/J xA/J
Data processing Data were loaded into the Rosetta Resolver? system (Rosetta Biosoftware, Seattle, WA) and processed using the RMA algorithm (http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=Retrieve&db=PubMed&list_uids=12582260). Intensities were calculated based on RMA, a Rosetta-developed error, and a MAS-5 p-value. The Rosetta-developed error is used in the calculation of xdev for the ratio p-values as described in section 2.2 (http://bioinformatics.oxfordjournals.org/cgi/content/full/22/9/1111).
 
Submission date Mar 16, 2010
Last update date Feb 02, 2011
Contact name Sergey Lezhnin
E-mail(s) sergey_lezhnin@merck.com
Organization name Merck Research Laboratories
Department Molecular Profiling
Lab Data Analysis
Street address 33 AVENUE LOUIS PASTEUR
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platform ID GPL7368
Series (2)
GSE20902 Affymetrix Mouse liver gene expression profiling of Cross B6/J x A/J
GSE20903 Mouse liver gene expression profiling of Cross B6/J x A/J

Data table header descriptions
ID_REF Rosetta generated unique probe identifier
VALUE Expression level
PVALUE P-value of expression level

Data table
ID_REF VALUE PVALUE
100017263_TGI_at 119.9742 6.4305e-026
100028120_TGI_at 196.3069 1.1956e-030
100016100_TGI_at 243.5392 2.4720e-032
100027781_TGI_at 31.3456 1.8730e-010
100001213_TGI_at 2745.5659 5.4623e-040
100035265_TGI_at 3.8554 1.1109e-001
100019771_TGI_at 61.8603 3.9205e-018
100009519_TGI_at 9.7698 2.8582e-003
100007713_TGI_at 269.9991 4.6787e-033
100034142_TGI_at 708.1859 1.2724e-037
100031799_TGI_at 17.6678 6.7428e-006
100035578_TGI_at 1209.6833 6.3872e-039
100011476_TGI_at 5.7637 3.9348e-002
100011176_TGI_at 78.6056 4.7559e-021
100019557_TGI_at 4800.5210 2.3379e-040
100003516_TGI_at 24.6155 2.8481e-008
100025710_TGI_at 14.0242 1.1852e-004
100012636_TGI_at 9.7409 2.9175e-003
100036860_TGI_at 398.2176 2.4749e-035
100020969_TGI_at 26.5977 6.2508e-009

Total number of rows: 32640

Table truncated, full table size 1178 Kbytes.




Supplementary file Size Download File type/resource
GSM522855.CEL.gz 3.2 Mb (ftp)(http) CEL
Processed data included within Sample table

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