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Sample GSM1360140 Query DataSets for GSM1360140
Status Public on Jun 01, 2014
Title TCam-2 - SE cell line
Sample type genomic
 
Source name testicular seminoma (Mizuno et al, 1993, de Jong et al,2008)
Organism Homo sapiens
Characteristics histological_subtype_primary tumor: seminoma
anatomical localisation: testis
cell line: TCam-2
Growth protocol Cells (wild type) were cultured in DMEM medium (Life Technologies, #31966-021) containing 10% fetal calf serum (FCS, Hyclone) in T75 cm2 flasks to 75-90% confluence.
Extracted molecule genomic DNA
Extraction protocol DNA was isolated using the DNeasy kit according to manufacturer’s instructions (QIAGEN, cat nr. 69504).
Label Cy3/Cy5
Label protocol Bisulfite conversion was performed using 500 ng genomic DNA input using the EZ DNA Methylation Gold Kit (Zymo Research).
 
Hybridization protocol The bisulfite converted DNA was processed and hybridized to the HumanMethylation450 BeadChip (Illumina, Inc.), according to the manufacturer's instructions.
Scan protocol The BeadChip images were scanned on the iScan system and the data was extracted into GenomeStudio software v2011.1, using default analysis settings.
Data processing Further processing was carried out in R using the LUMI package [1] following the optimized “lumi: QN+BMIQ” pipeline [2] This includes exclusion of poorly performing probes (p<0.01), color adjustment, quantile normalization and correction for probe type bias (Infinium I vs II) using the BMIQ algorithm [3]. 1. Du, P., W.A. Kibbe, and S.M. Lin, lumi: a pipeline for processing Illumina microarray. Bioinformatics, 2008. 24(13): p. 1547-8. 2. Marabita, F., et al., An evaluation of analysis pipelines for DNA methylation profiling using the Illumina HumanMethylation450 BeadChip platform. Epigenetics, 2013. 8(3): p. 333-46. 3. Teschendorff, A.E., et al., A beta-mixture quantile normalization method for correcting probe design bias in Illumina Infinium 450 k DNA methylation data. Bioinformatics, 2013. 29(2): p. 189-96.
 
Submission date Mar 31, 2014
Last update date Jun 13, 2014
Contact name Martin Anne Rijlaarsdam
E-mail(s) m.a.rijlaarsdam@gmail.com
Phone 0031645408508
Organization name Erasmus MC
Department Pathology
Lab Laboratory for Experimental Patho-Oncology (LEPO)
Street address Wytemaweg 80
City Rotterdam
ZIP/Postal code 3015 CN
Country Netherlands
 
Platform ID GPL13534
Series (2)
GSE56382 Seminoma and embryonal carcinoma footprints identified by analysis of integrated genome-wide epigenetic and expression profiles of germ cell cancer cell lines (methylation data).
GSE56454 Seminoma and embryonal carcinoma footprints identified by analysis of integrated genome-wide epigenetic and expression profiles of germ cell cancer cell lines

Data table header descriptions
ID_REF
VALUE Normalized Beta (see data processing for normalization method)
Detection Pval

Data table
ID_REF VALUE Detection Pval
cg00000029 0.18974347601908 0
cg00000108 0.973711886446562 0
cg00000109 0.942190195234031 0
cg00000165 0.819239299816868 0
cg00000236 0.84117139903284 0
cg00000289 0.690426575723715 0
cg00000292 0.849687499417287 0
cg00000321 0.887023599061824 0
cg00000363 0.472843275768785 0
cg00000622 0.0233896076549863 0
cg00000658 0.866289011827529 0
cg00000714 0.0786948753329386 0
cg00000721 0.970564190415886 0
cg00000734 0.030394120013751 0
cg00000769 0.0605662955384453 0
cg00000807 0.824009033043132 0
cg00000884 0.88077124445222 0
cg00000905 0.0270464117487655 0
cg00000924 0.65328347609326 0
cg00000948 0.799459366559121 0

Total number of rows: 484318

Table truncated, full table size 14803 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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