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Sample GSM1317010 Query DataSets for GSM1317010
Status Public on Jun 12, 2014
Title GM01651_miR
Sample type RNA
 
Source name primary fibroblast cells
Organism Homo sapiens
Characteristics cell line: GM01651
cell type: primary fibroblast
blm mutation: homozygous (1544insA of RECQL3 gene)
clinical features: Bloom syndrome
age: 13
gender: F
Biomaterial provider Coriell Cell Repositories http://ccr.coriell.org/Sections/Search/Search.aspx?PgId=165&q=NA01651
Extracted molecule total RNA
Extraction protocol Total RNA samples from fibroblasts were isolated using Qiagen’s miRNAeasy Mini Kit (Qiagen, Valencia, CA). RNA quality was assessed using the Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto, CA), and only samples of high quality, defined by distinct 28S and 18S rRNA bands together with a RIN (RNA integrity number) > 7, were used for further analyses.
Label biotin
Label protocol total RNA (5 micro-g) was converted to biotin-labeled complementary DNA, hybridized onto the chips, and processed by direct detection of the biotin-containing transcripts by streptavidin-Alexa 647 conjugate through a core facility in the Laboratory of Molecular Technology (NCI-Frederick) according to the manufacturer's instructions.
 
Hybridization protocol The standard hybridization protocol was used as recommended by a custom miRNA microarray chip (OSU-CCC version 4.0).
Scan protocol GeneChips were scanned using the Axon 4000B Scanner through the Laboratory of Molecular Technology (NCI-Frederick).
Description primary human fibroblasts
Data processing Genepix (version Pro 6.0.1.00)
 
Submission date Jan 29, 2014
Last update date Sep 05, 2017
Contact name James William MacDonald
E-mail(s) jmacdon@uw.edu
Organization name University of Washington
Department Environmental and Occupational Health Sciences
Street address 4225 Roosevelt Way NE
City Seattle
State/province WA
ZIP/Postal code 98105-6099
Country USA
 
Platform ID GPL14592
Series (2)
GSE54502 Bloom syndrome protein modulates protein-coding gene and miRNA expression as a function of G4 DNA content
GSE62877 Werner syndrome WRN helicase alters gene expression in a G-quadruplex DNA-dependent manner to antagonize a pro-senescence gene expression program

Data table header descriptions
ID_REF
VALUE F635.Median...B635

Data table
ID_REF VALUE
1 31913
2 29581
3 215
4 239
5 128
6 372
7 675
8 615
9 815
10 705
11 321
12 257
13 374
14 535
15 -18
16 23
17 618
18 558
19 6936
20 6737

Total number of rows: 10240

Table truncated, full table size 83 Kbytes.




Supplementary file Size Download File type/resource
GSM1317010_P833_37_GM01651_pmt800_10032007.gpr.gz 486.0 Kb (ftp)(http) GPR
Processed data included within Sample table

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