NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM410656 Query DataSets for GSM410656
Status Public on Sep 30, 2009
Title skin-biopsy-patient2-repA
Sample type RNA
 
Source name normal skin biopsy
Organism Homo sapiens
Characteristics gender: male
tissue: skin
patient_replicate: 2
technical_replicate: A
Growth protocol Fresh frozen KS and skin biopsies were obtained from the NIH AIDS Cancer Specimen Resource Bank (USA) and from Chelsea and Westminster Hospital (UK). All participants were male, HIV–infected and between the ages of 26 and 58. Three out of five biopsies were collected in London in 2008. The remaining biopsies were nodular stage KS and collected in the U.S.A in 2003. All participants were undergoing anti-retroviral treatment at the time of collection.
Extracted molecule total RNA
Extraction protocol Tissue was disrupted and homogenized using a mechanical rotor and RNA subsequently extracted using the miRNeasy mini kit (Qiagen) according to manufacturer’s instructions. The small RNA fraction was assessed using the Agilent small RNA Kit. Quality and integrity of the RNA fraction between 6 and 150 nucleotides was quantified using the Agilent 2100 bioanalyzer (Agilent).
Label Cy3
Label protocol Total RNA was labelled with Cy3 using the Agilent miRNA labelling and reagent kit as per manufacturer's instructions.
 
Hybridization protocol Cy3 labelled total RNA was hybridised to Agilent Human miRNA Microarray v1.0 as per manufacturer's instructions.
Scan protocol The Agilent Human miRNA Microarray was scanned using the Agilent scanner as per manufacturer's instructions.
Description P2skin
Data processing Summary expression text files were created using Agilent Feature Extraction Software. From the summary text files we extracted the median (gMedianSignal) and background signal-(gBGUsed). The arrays were then background corrected using the 'normexp' function of the limma package and quantile normalized to each other.
 
Submission date May 31, 2009
Last update date Aug 24, 2009
Contact name Stephen Henderson
E-mail(s) s.henderson@ucl.ac.uk
Phone 02076796827
Fax 02076796851
Organization name UCL
Department Cancer Institute
Lab Viral Oncology
Street address Paul O'Gorman Building, Huntley Street
City London
ZIP/Postal code WC1E 6BT
Country United Kingdom
 
Platform ID GPL8617
Series (2)
GSE16353 The profile of cellular and KSHV microRNAs in AIDS_KS biopsies (and normal skin control biopsies)
GSE16357 Effects of HHV8 infection in lymphatic endothelial cells

Data table header descriptions
ID_REF
VALUE normalised log2 expression values

Data table
ID_REF VALUE
DarkCorner 5.446025272
NC1_00000197 5.075333717
NC1_00000215 5.155841336
NC2_00079215 4.99041225
NC2_00092197 5.156406698
NC2_00106057 5.157288709
NC2_00122731 4.991503784
(-)3xSLv1 4.995329383
SCorner3 5.501366775
dmr_285_19 4.983425241
dmr_285_18 5.080422204
dmr_3_17 5.159024495
dmr_3_16 5.160265081
dmr_308_21 5.107278448
dmr_308_22 5.080925644
dmr_316_22 5.186823969
dmr_316_21 5.081397275
dmr_31a_19 5.12120961
dmr_31a_18 4.996516819
dmr_6_22 5.107905829

Total number of rows: 1555

Table truncated, full table size 40 Kbytes.




Supplementary file Size Download File type/resource
GSM410656.txt.gz 1.3 Mb (ftp)(http) TXT
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap