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Status |
Public on Dec 01, 2013 |
Title |
tumor cells NLPHL 9 |
Sample type |
RNA |
|
|
Source name |
tumor cells NLPHL
|
Organism |
Homo sapiens |
Characteristics |
cell type: tumor cells NLPHL
|
Treatment protocol |
Cells were microdissected from HE stained kryosections
|
Extracted molecule |
total RNA |
Extraction protocol |
RNA was amplified using the One-direct-Kit from NUGEN applied for 250 microdissected cells
|
Label |
biotin
|
Label protocol |
Samples were labelled with Encore biotin module (NUGEN) washed and stained using the HWS Kit (Affymetrix).
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|
|
Hybridization protocol |
Human Gene 1.0 ST arrays (Affymetrix) were hybridized with 5.5 mg labelled cDNA.
|
Scan protocol |
Affymetrix Gene ChIP Scanner 3000 7G
|
Description |
NLPHL9
|
Data processing |
Statistical analysis was done with the statistical computing environment R. Additional software packages (affy, geneplotter, multtest, and vsn) were taken from the Bioconductor project. Microarray preprocessing: Probe level normalization was conducted using the variance stabilization method (vsn) from Huber et al.. probe group file: unsupported Human Gene 1.0 ST Array CDF Files meta-probeset file: HuGene-1_0-st-v1 Probeset Annotations, CSV Format, Release 30 (11 MB 01/22/10)
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Submission date |
May 17, 2013 |
Last update date |
Dec 01, 2013 |
Contact name |
Claudia Döring |
E-mail(s) |
[email protected]
|
Organization name |
Johann Wolfgang-Goethe University Frankfurt a.M.
|
Department |
Medical School, Institite of Pathology
|
Street address |
Theodor Stern Kai 7
|
City |
Frankfurt |
ZIP/Postal code |
60590 |
Country |
Germany |
|
|
Platform ID |
GPL6244 |
Series (1) |
GSE47044 |
Nodular lymphocyte predominant hodgkin lymphoma and T cell/histiocyte rich large B cell lymphoma - endpoints of a spectrum of one disease? |
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