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Sample GSM3543895 Query DataSets for GSM3543895
Status Public on Jan 06, 2020
Title muscle_notimmunized_CRC305E92725_3h
Sample type RNA
 
Source name muscle,RNAlater
Organism Homo sapiens
Characteristics protocol: CRC305E
treatment: FLUADE
injected leg: left
day: 0
hour: 3
tissue: muscle
biopsied leg: right
biopsy site treatment: not immunized
biopsy comments: muscle tissue
participant: CRC305E92725
gender: male
age: 25y
race: white
ethnicity: not hispanic or latino
Treatment protocol Microarray experiments were performed as single-color hybridization. Cyanine-3 (Cy3) labeled cRNA was prepared from 100 ng total RNA extracted from the whole blood in PaxGene tubes or the muscle biopsies stored in RNAlater 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 600ng 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 not immunized muscle biopsy gene expression of participant CRC305E92725 at 3 hours post immunization
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.
Quantile normalized signal intensity using limma 3.38.3, read.maimages source = agilent, backgroundCorrect method= normexp, normalizeBetweenArrays method= quantile
 
Submission date Jan 07, 2019
Last update date Jan 07, 2020
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)
GSE124719 Gene expression signatures in blood and muscle biopsy after intramuscular immunization of healthy adult humans with adjuvanted vaccines (BIOVACSAFE protocol 305E)

Data table header descriptions
ID_REF
VALUE Quantile normalized signal intensity

Data table
ID_REF VALUE
1 15.720924258811943
2 4.56490962478184
3 3.04437595339938
4 8.901468641012602
5 6.825390571300767
6 4.345292703491113
7 6.62650034976342
8 3.8850738272631284
9 11.494148718254833
10 7.465917497777421
11 7.412526106743439
12 5.256428865490724
13 4.435587792660363
14 3.7449753799877974
15 3.5928036826335106
16 8.641727862341174
17 3.4254845243697583
18 4.435587792660363
19 4.345292703491113
20 9.952014795496723

Total number of rows: 62975

Table truncated, full table size 1482 Kbytes.




Supplementary file Size Download File type/resource
GSM3543895_US22502595_254890810582_S01_GE1_1105_Oct12_2_2.txt.gz 12.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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