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Sample GSM1713944 Query DataSets for GSM1713944
Status Public on Oct 01, 2015
Title 140156A_NM76
Sample type RNA
 
Source name peripheral blood_never-smoker
Organism Homo sapiens
Characteristics gender: male
age: 27y
smoking status: never-smoker
tissue: peripheral blood
Treatment protocol 4 mL peripheral venous fasting blood was collected from each subject in EDTA anticoagulant tube. The blood samples were maintained at room temperature for 30 minutes and then centrifuged at 1500g for 15min at 4℃. Then plasma was transferred to another clean EP tube and stored at – 80 ℃ until RNA extraction. Then, the total RNA was extracted from the plasma using the miRNeasy Mini Kit (Qiagen, Hilden, Germany), according to the manufacturer’s protocol. The quality and quantity of RNA were measured with a NanoDrop spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).plasma miRNA expression profiles were determined using the human microRNA array version 19.0 (Agilent, USA). Plasma miRNA from 28 present smokers and 12 never -smokers were detected with the miRNA array respectively.
Growth protocol All subjects are from the same unit , do the same job, and live in the same community .
Extracted molecule total RNA
Extraction protocol RNA was prepared using Qiagen miRNeasy Mini kit following the manufacturer's recommendations. RNA was quantified using a NanoDrop-1000 spectrophotometer and quality was monitored with the Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA).
Label Cy3
Label protocol Labeled RNAs were heat denatured and hybridized to Agilent miRNA microarray, according to manufacturer's protocol.
 
Hybridization protocol According to the Agilent miRNA Microarray Protocol (Agilent Technologies).
Scan protocol After hybridization and post-hybridization washes, slides were scanned immediately in Agilent Microarray Scanner with Surescan High Resolution Technology (Agilent Technologies, Santa Clara, CA).
Description Gene expression in never-smoker plasma
Data processing Feature Extraction v10.7.3.1 (Agilent Technologies, CA) software was used to extract all features of the data obtained from the scanned images and Bioconductor software was used to analyze the raw data, which are normalized by percentile normalization.
 
Submission date Jun 17, 2015
Last update date Oct 01, 2015
Contact name zhang suwei
E-mail(s) suweizhang@capitalbio.com
Phone 01080729390
Organization name capitalbio
Street address changping
City beijing
ZIP/Postal code 102206
Country China
 
Platform ID GPL18402
Series (1)
GSE69960 Cigarette smoking alters plasma microRNA expression profile in healthy young male smokers

Data table header descriptions
ID_REF
VALUE The noromalized value of 90 percentile

Data table
ID_REF VALUE
Blank -7.1771355
NC1_00000197 -7.1771355
NC1_00000215 -7.1771355
NC2_00079215 -7.1771355
NC2_00092197 -7.1771355
NC2_00106057 -7.1771355
NC2_00122731 -7.1771355
NegativeControl -7.1771355
dmr_285 7.6974344
dmr_3 8.549569
dmr_308 -7.1771355
dmr_316 -7.1771355
dmr_31a 6.043046
dmr_6 8.064584
hsa-let-7a-3p -7.1771355
hsa-let-7a-5p -0.57069516
hsa-let-7b-3p -7.1771355
hsa-let-7b-5p 1.2049868
hsa-let-7c -1.5791845
hsa-let-7d-3p -3.4796844

Total number of rows: 2027

Table truncated, full table size 50 Kbytes.




Supplementary file Size Download File type/resource
GSM1713944_US10313827_254606412995_S01_miRNA_1105_Oct12_2_2.txt.gz 3.2 Mb (ftp)(http) TXT
Processed data included within Sample table

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