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Sample GSM188662 Query DataSets for GSM188662
Status Public on Nov 27, 2009
Title NLPHL_lymph_node_case1
Sample type RNA
 
Source name lymph node affected by NLPHL
Organism Homo sapiens
Characteristics Gender: male, Age: 49, Tissue: lymph node taken at diagnosis affected by nodular lymphocyte predominant Hodgkin's lymphoma, An Arbor Stage: IA, follow-up: 10 years; status at last follow-up: died of squamous cell carcinoma of the larynx
Biomaterial provider Department of pathology, University Hospitals Leuven
Treatment protocol tissue blocs were kept at -80° till use
Growth protocol Fresh frozen tissue blocs were kept at -80° till use. They were transported on dry ice to the cryostat where a number (depending on the size of the bloc) of 20 micron thick sections were cut and put into a labeled, 2.0 ml microcentrifuge tube. At the end an extra 3 micron thick section was taken for HE staining.
Extracted molecule cytoplasmic RNA
Extraction protocol Total RNA was extracted from 20 micron sections of each frozen tissue sample, using the TriZol reagent (Invitrogen, Merelbeke, Belgium) followed by purification using the RNaesy mini kit (Qiagen, Venlo, The Netherlands), according to the manufacturers recommendations. RNA quality, integrity and concentration were measured using a nanodrop spectrophotometer (Nanodrop Technologies, Wilmington, DE, USA).
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 microg total RNA.
 
Hybridization protocol Following fragmentation, 10 microg of cRNA were hybridized for 16 hr at 45C and at 60 rounds/min. The GeneChips were washed and stained in the Affymetrix Fluidics Station 400 and 450.
Scan protocol GeneChips were scanned using the GeneChip Scanner 3000 7G.
Description Nodular lymphocyte predominant Hodgkin's lymphoma affecting a lymph node
Data processing Data were normalized using GC-RMA. The package gcrma in Bioconductor was used for this (R version 2.3.1)
 
Submission date May 14, 2007
Last update date Aug 28, 2018
Contact name Rekin's Janky
E-mail(s) Nucleomics.Bioinformatics@vib.be
Organization name VIB
Department Nucleomics Core
Street address Herestraat 49 Box 816
City Leuven
ZIP/Postal code B-3000
Country Belgium
 
Platform ID GPL570
Series (1)
GSE7788 Nodular lymphocyte predominant Hodgkin's lymphoma vs T cell/histiocyte rich B cell lymphoma
Relations
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE Data were normalized using GC-RMA. The package gcrma in Bioconductor was used for this (R version 2.3.1).
ABS_CALL the call in an absolute analysis that indicates if the transcript was present (P), absent (A), marginal (M), or no call (NC)
DETECTION P-VALUE 'detection p-value', p-value that indicates the significance level of the detection call

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
1007_s_at 5.325871639 P 0.004863
1053_at 8.460957258 P 0.000805
117_at 3.95938636 P 0.004863
121_at 4.325506537 P 0.004863
1255_g_at 2.094799087 A 0.458816
1294_at 7.692793645 P 0.000266
1316_at 3.115138544 P 0.011447
1320_at 2.495496777 A 0.781017
1405_i_at 12.16244311 P 0.000491
1431_at 2.800864397 P 0.039365
1438_at 2.165984892 A 0.541184
1487_at 7.456105311 P 0.02786
1494_f_at 2.164707679 M 0.05447
1552256_a_at 8.464703244 P 0.002924
1552257_a_at 7.317201132 P 0.00222
1552258_at 2.754506862 P 0.04558
1552261_at 2.614768836 A 0.106612
1552263_at 7.921394252 P 0.001673
1552264_a_at 8.518652456 P 0.001673
1552266_at 2.734131881 A 0.266847

Total number of rows: 54675

Table truncated, full table size 1788 Kbytes.




Supplementary file Size Download File type/resource
GSM188662.CEL.gz 4.8 Mb (ftp)(http) CEL
Processed data included within Sample table

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