|
Status |
Public on Sep 14, 2015 |
Title |
Tumor biopsy (P-386) |
Sample type |
genomic |
|
|
Source name |
Cervical tumor
|
Organism |
Homo sapiens |
Characteristics |
figo stage: 3B histology: Squamous cell carcinoma cohort: cohort 2
|
Treatment protocol |
The samples were immediately snap-frozen in liquid nitrogen and stored at -80 C until used for analysis.
|
Growth protocol |
1-4 tumor samples wer collected from each patient at the time of diagnosis
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Genomic DNA was extracted according to a standard protocol with proteinase K, phenol, chloroform and isoamylalcohol (cohort 1) or by the use of Purelink Genomic DNA Mini Kit (cohort 2)
|
Label |
biotin and DNP
|
Label protocol |
Standard Illumina Protocol
|
|
|
Hybridization protocol |
Bisulphite converted DNA was amplified, fragmented and hybridised to Illumina Infinium Human Methylation450 Beadchip using standard Illumina protocol
|
Scan protocol |
Arrays were imaged using BeadArray Reader using standard recommended Illumina scanner setting
|
Data processing |
Data processing was performed using the pipeline developed by Touleimat and Tost 2012.
|
|
|
Submission date |
May 05, 2015 |
Last update date |
Sep 14, 2015 |
Contact name |
Heidi Lyng |
E-mail(s) |
heidi.lyng@rr-research.no
|
Phone |
4722781478
|
Organization name |
Oslo University Hospital
|
Department |
Department of Radiation Biology
|
Street address |
Montebello
|
City |
Oslo |
ZIP/Postal code |
0310 |
Country |
Norway |
|
|
Platform ID |
GPL13534 |
Series (1) |
GSE68339 |
Interplay between promoter methylation and chromosomal loss in gene silencing at 3p11-p14 in cervical cancer |
|