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Sample GSM147045 Query DataSets for GSM147045
Status Public on Jan 01, 2007
Title MM-077_3
Sample type RNA
 
Source name Human multiple myeloma patient MM-077
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: M; Age: 62; Stage: II A; MC: 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-077
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 310.111932
1053_at 53.38787
117_at 93.235912
121_at 476.894235
1255_g_at 20.827692
1294_at 477.008316
1316_at 54.277414
1320_at 27.429629
1405_i_at 38.248245
1431_at 24.219863
1438_at 135.909721
1487_at 282.766574
1494_f_at 160.099292
1598_g_at 605.823459
160020_at 232.641517
1729_at 337.130705
1773_at 84.90109
177_at 46.424043
179_at 492.392235
1861_at 89.895416

Total number of rows: 22283

Table truncated, full table size 465 Kbytes.




Supplementary file Size Download File type/resource
GSM147045.cel.gz 3.4 Mb (ftp)(http) CEL

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