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Sample GSM1488677 Query DataSets for GSM1488677
Status Public on Aug 01, 2015
Title TCam-2-2w-1
Sample type genomic
 
Source name Seminoma-like cell line
Organism Homo sapiens
Characteristics strain: CD1 nude mice
age: 6 weeks at start of xenografting
tissue: Seminoma-like
Growth protocol cultivation protocol: TCam-2 and 2102EP cells were cultivated as published (Nettersheim et al., 2013, PubMed ID: 24386123)
xenografting protocol: 1x10^7 TCam-2 and 2102EP cells were xenografted in CD1 nude mice as published previously (Nettersheim et al., 2012, Pubmed ID: 22489004)
Extracted molecule genomic DNA
Extraction protocol Genomic DNA was isolated by phenol / chloroform / isoamylalcohol isolation as published (Nettersheim et al., 2013, Pubmed ID: 24386123). Quality control was performed with Agilent Bioanalyser.
bisulfite convesion: Genomic DNA was bisulfite converted using the EZ DNA methylation kit according to the manual (Zymo Research) and as published (Nettersheim et al., 2013, Pubmed ID: 24386123)
Label biotin
Label protocol Biotinylated cRNA were prepared with the Ambion MessageAmp kit for Illumina arrays
 
Hybridization protocol Standard Illumina hybridization protocol
Scan protocol Standard Illumina scanning protocol
Description biological replicate 1
Data processing A subset quantile normalization approach developed by N. Touleimat & J. Tost was applied (Touleimat, Tost, 2012, Pubmed ID: 22690668 ). This processing pipeline includes signal correction for the adjustment of the color balance and background level correction as well as the Infinium I/Infinium II shift correction between sample normalization. Technical quality parameters such as hybridization, extension, bisulfite conversion and specificity were evaluated using the ‚Genome Studio’ software. Beta-value signal distributions were inspected by density plots. Data was analysed using ‚Bioconductor R’ (http://www.bioconductor.org). To increase performance in terms of detection and true positive rate of highly methylated and unmethylated CpG-sites, beta-values were transformed to M-values (Du et al., 2010, Pubmed ID: 21118553)
 
Submission date Aug 26, 2014
Last update date Aug 01, 2015
Contact name Daniel Nettersheim
E-mail(s) Daniel.nettersheim@med.uni-duesseldorf.de
Organization name University Hospital Düsseldorf
Department Urology
Lab Urological Research Lab, Translational Urooncology
Street address Universitätsstr. 1
City Düsseldorf
State/province NRW
ZIP/Postal code 40225
Country Germany
 
Platform ID GPL13534
Series (1)
GSE60787 Genome-wide DNA methylation analysis of seminoma-like TCam-2 cells during transition into an embryonal carcinoma-like state

Data table header descriptions
ID_REF
VALUE Quantile normalized. Values were transformed in % methylation.
Detection Pval

Data table
ID_REF VALUE Detection Pval
cg00000029 0.120231383 0
cg00000108 0.956617162 0
cg00000109 0.893267483 0
cg00000165 0.330188279 0
cg00000236 0.769664608 0
cg00000289 0.68493248 0
cg00000321 0.584597473 0
cg00000363 0.066377775 0
cg00000622 0.019307245 0
cg00000658 0.890449844 0
cg00000714 0.070450398 0
cg00000721 0.918871071 0
cg00000734 0.042355928 0
cg00000769 0.088969013 0
cg00000807 0.3427692 0
cg00000884 0.856350563 0
cg00000905 0.047838804 0
cg00000924 0.177503205 0
cg00000948 0.565945147 0
cg00000957 0.775490779 0

Total number of rows: 468317

Table truncated, full table size 11399 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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