NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM3555765 Query DataSets for GSM3555765
Status Public on Jan 07, 2022
Title WholeBlood_CRC305D2GENT098213_Day7
Sample type RNA
 
Source name Peripheral Blood, PaxGene
Organism Homo sapiens
Characteristics tissue: whole blood
protocol: CRC305D2
treatment: BOOSTRIX
day: 7
participant: CRC305D2GENT098213
gender: male
age: 28y
race: white
ethnicity: not hispanic or latino
recent boostrix: 1
Treatment protocol Microarray experiments were performed as single-color hybridization. Cyanine-3 (Cy3) labeled cRNA was prepared from 100 ng total RNA using the One-Color Low RNA Input Linear Amplification PLUS kit (Agilent) according to the manufacturer's instructions, followed by RNAeasy column purification (QIAGEN, Valencia, CA). Dye incorporation and cRNA yield were checked with the NanoDrop ND-1000 Spectrophotometer.
Extracted molecule total RNA
Extraction protocol mRNA was reverse transcribed and amplified using an oligo-dT-T7 promoter primer
Label Cy3
Label protocol Total RNA was amplified and labeled with the low input Quick-Amp Labelling Kit (Agilent Technologies) with cyanine 3-CTP followed by precipitation, purification, and quantification.
 
Hybridization protocol 600 ng of Cy3-labelled cRNA (specific activity >10.0 pmol Cy3/ug cRNA) was fragmented and hybridized to custom whole genome human 8 × 60K multipack microarrays (Agilent-048908) following the manufacturers instructions. After hybridization, microarrays were washed 1 minute at room temperature with GE Wash Buffer 1 (Agilent) and 1 minute with 37°C GE Wash buffer 2 (Agilent) according the manufacturers protocol.
Scan protocol Slides were scanned immediately after washing using a high resolution DNA Microarray Scanner (G2505B, Agilent Technologies) with 3 µm resoltion and 20 bit image depth
Description Whole blood gene expression of BOOSTRIX treated participant CRC305D2GENT098213 on day 7
Data processing The scanned microarray images were processed with the Image Analysis/Feature Extraction software G2567AA v. A.11.5.1.1 (Agilent Technologies) using default settings and the GE1_1105_Oct12 extraction protocol.
 
Submission date Jan 09, 2019
Last update date Jan 07, 2022
Contact name David Lewis
E-mail(s) djmlewis@hotmail.com
Organization name Imperial College London
Department ICRF
Street address Du Cane Road
City London
ZIP/Postal code W12 0NN
Country United Kingdom
 
Platform ID GPL21272
Series (1)
GSE124842 Gene expression signatures after immunisation with Boostrix - alum adsorbed tetanus toxoid, reduced diphtheria toxoid and acellular pertussis vaccine (BIOVACSAFE protocol 305D2)

Data table header descriptions
ID_REF
VALUE Quantile normalized signal intensity using limma 3.38.3, read.maimages source = agilent.median, backgroundCorrect method= normexp, normalizeBetweenArrays method= quantile

Data table
ID_REF VALUE
1 17.010640917499433
2 3.4009844070667077
3 2.2489128340434985
4 10.899466312928723
5 5.906571353013602
6 3.921293013448379
7 6.597644791641641
8 4.744229020376755
9 13.052828501311359
10 5.32657168687877
11 2.8253051012953954
12 7.502760262752579
13 3.921293013448379
14 3.921293013448379
15 5.382443901023588
16 7.869659466987013
17 3.232880372565729
18 3.8045678708853536
19 5.298020921551981
20 9.229625203690638

Total number of rows: 62975

Table truncated, full table size 1485 Kbytes.




Supplementary file Size Download File type/resource
GSM3555765_US22502595_254890810821_S01_GE1_1105_Oct12_1_1.txt.gz 12.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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