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Sample GSM967107 Query DataSets for GSM967107
Status Public on Oct 12, 2012
Title Primary Plasma Cell Leukemia PCL-021 Expression
Sample type RNA
 
Source name Primary Plasma Cell Leukemia PCL-021
Organism Homo sapiens
Characteristics cell type: plasma cell
disease state: plasma cell leukemia
genome variation: translocation t(4;14)
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 5.5 micrograms of single-stranded DNA target obtained from 100 ng of purified total RNA was fragmented and then labeled using the WT Terminal Labeling Kit according to the standard Affymetrix protocol (GeneChip® Whole Transcript (WT) Sense Target Labeling Assay Manual).
 
Hybridization protocol The fragmented labeled single-stranded DNA target was hybridized for 16 hours and 30 minutes at 45°C on GeneChip® Gene 1.0 ST array according to the standard Affymetrix protocol.
Scan protocol Washing and scanning were performed using GeneChip System of Affymetrix (GeneChip Hybridization Oven 640, GeneChip Fluidics Station 450 and GeneChip Scanner 7G).
Description main IgH chromosomal translocations t(11;14), t(4;14), t(14;16), t(14;20)
Gene expression profiling data from human multiple myeloma patient PCL-021
Data processing Log2-transformed expression values were extracted from CEL files and normalized using NetAffx Transcript Cluster Annotations, Release 31 and robust multi-array average (RMA) procedure in Expression Console software (Affymetrix Inc.). The expression values of transcript cluster ID specific for loci representing naturally occurring read-through transcriptions were summarized as median value for each sample.
 
Submission date Jul 16, 2012
Last update date Oct 13, 2012
Contact name Luca Agnelli
E-mail(s) luca.agnelli@istitutotumori.mi.it, luca.agnelli@gmail.com
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 GPL6244
Series (2)
GSE39381 Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with transcriptional Profile alterations (Expression)
GSE39383 Genome-wide analysis of primary plasma cell leukemia identifies recurrent imbalances associated with transcriptional Profile alterations

Data table header descriptions
ID_REF
VALUE log2 transformed RMA-calculated Signal intensity

Data table
ID_REF VALUE
7896736 5.569146
7896738 2.422442
7896740 2.473915
7896742 6.61545
7896744 4.616177
7896746 8.072744
7896748 9.64547
7896750 4.774399
7896752 9.514872
7896754 7.967271
7896756 4.171264
7896759 6.229674
7896761 6.330952
7896779 6.50441
7896798 6.918526
7896817 6.260939
7896822 5.855729
7896859 4.857871
7896861 3.64204
7896863 5.586564

Total number of rows: 33297

Table truncated, full table size 549 Kbytes.




Supplementary file Size Download File type/resource
GSM967107_PCL-021_GENE1.0_1.CEL.gz 3.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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