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Sample GSM147047 Query DataSets for GSM147047
Status Public on Jan 01, 2007
Title MM-079_3
Sample type RNA
 
Source name Human multiple myeloma patient MM-079
Organism Homo sapiens
Characteristics Legend: Age = age at diagnosis; Stage = stage at diagnosis; MC = monoclonal component; BL = bone lesions
Legend: TC classification = TC1, TC2, TC3, TC4, TC5 (Hideshima et al. Blood, 2004; Agnelli et al., J.Clin.Oncol., 2005); +11 = chromosome 11 trisomy; +19 = chromosome 19 trisomy; HD = hyperdiploidy status; del(13) = chromosome 13 deletion; +1q = chromosome 1q gain.
Sex: F; Age: 72; Stage: II A; MC: Gk + Gl; BL: +
TC: 2; +11: +; +19: +; HD: +; del(13): -; +1q: -
Treatment protocol Plasma cells were purified from bone marrow samples using CD138 immunomagnetic microbeads according to the manufacturer's instructions (MidiMACS system, Miltenyi Biotec); the purity of the positively selected PCs was assessed by morphology and flow cytometry and was > 90% in all cases
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions (Gibco BRL). RNA was purified using the Rneasy Mini Kit according to the manufacturer's instruction (Qiagen).
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 micrograms of total RNA (Expression Analysis Technical Manual, Affymetrix).
 
Hybridization protocol Following fragmentation, 15 micrograms of cRNA were hybridized for 16 hr and 30 minutes at 45°C on GeneChip HG-U133A Arrays. GeneChips were washed and stained in the Affymetrix Fluidics Station 450.
Scan protocol HG-U133A arrays were scanned using the Agilent GeneArray Scanner G2500A (Affymetrix).
Description Gene expression profiling data from human multiple myeloma patient MM-079
Data processing The probe-level signals were converted to expression values using the Bioconductor function for Robust Multi-array Analysis (RMA), in which perfect match intensities are background adjusted, normalized by means of quantile-quantile normalization, and log2 transformed..
 
Submission date Nov 24, 2006
Last update date Dec 28, 2006
Contact name Luca Agnelli
E-mail(s) [email protected], [email protected]
Phone +390223903581
Organization name IRCCS Istituto Nazionale dei Tumori
Department Department of Advanced Diagnostics
Street address Venezian 1
City MILAN
ZIP/Postal code 20133
Country Italy
 
Platform ID GPL96
Series (1)
GSE6365 Distinct transcriptional and genetic features associated with chromosome 13 deletion in multiple myeloma

Data table header descriptions
ID_REF
VALUE RMA-calculated Signal intensity

Data table
ID_REF VALUE
1007_s_at 213.133619
1053_at 46.811009
117_at 103.334089
121_at 509.418467
1255_g_at 22.896844
1294_at 344.182802
1316_at 50.864066
1320_at 22.911786
1405_i_at 43.17338
1431_at 25.598994
1438_at 155.501698
1487_at 382.813817
1494_f_at 177.478775
1598_g_at 1614.92116
160020_at 187.322213
1729_at 288.511874
1773_at 95.930761
177_at 50.782699
179_at 442.793931
1861_at 130.197663

Total number of rows: 22283

Table truncated, full table size 464 Kbytes.




Supplementary file Size Download File type/resource
GSM147047.cel.gz 3.3 Mb (ftp)(http) CEL

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