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Sample GSM318887 Query DataSets for GSM318887
Status Public on Oct 30, 2008
Title PHA stimulated, Tempus, replicate Y (Blood_PHA25_ABI_Y)
Sample type RNA
 
Source name Peripheral blood
Organism Homo sapiens
Characteristics n/a
Treatment protocol Whole blood from 7 healthy individuals was collected using Li Heparin tubes, and was incubated for 3 hours at room temperature with or without addition of 25 ug/mL of PHA. After incubation, samples were subsequently transferred to either Tempus or PAXgene tubes.
Extracted molecule total RNA
Extraction protocol RNA was extracted at the ITN Central Nucleic Acid Isolation Core facility, Pittsburgh, PA according to the ITN modified method for Tempus. Whole blood samples collected into Tempus vacuette were extracted using ABI Prism 6100 Nucleic Acid PrepStation and using Tempus extraction reagents. The PAXgene whole blood sample were processed using the PAXgene Blood RNA Kit based on the Qiagen method for column purification of nucleic acid.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol. cRNA target amplificationwas performed using the Affymetrix In-vitro Transcription (IVT) Kit followed by a Globin Reduction step.
 
Hybridization protocol Hybridization on Affymetrix HG-U133 2.0 plus array according to manufacturer's instructions.
Scan protocol GeneChips were scanned using the Hewlett-Packard GeneArray Scanner G2500A.
Description PHA stimulated, Tempus RNA extraction method, replicate Y
Data processing The data normalizaion was performed using Bioconductor package THREESTEP(background.method="MASIM", noemalize.method="scaling", summary.method="tukey.biweight").
 
Submission date Sep 09, 2008
Last update date Aug 28, 2018
Contact name Zhong Gao
Organization name Johns Hopkins University
Street address Ross 844 720 Rutland Avenue
City Baltimore
State/province MD
ZIP/Postal code 21205
Country USA
 
Platform ID GPL570
Series (2)
GSE12709 Differential gene expression profiles are dependent upon method of peripheral blood RNA isolation (PHA)
GSE12711 Differential gene expression profiles are dependent upon method of peripheral blood RNA isolation
Relations
Reanalyzed by GSE119087

Data table header descriptions
ID_REF
VALUE Normalized intensity value

Data table
ID_REF VALUE
1007_s_at 4.88831763783175
1053_at 4.52696551871218
117_at 6.06982358558836
121_at 6.25494151195607
1255_g_at -0.687591468238494
1294_at 4.97803246110343
1316_at 3.76128992249248
1320_at 0.264510330643565
1405_i_at 10.3621357040439
1431_at 2.58838729916668
1438_at 3.42571099300536
1487_at 5.43876237534366
1494_f_at 4.36842266552008
1552256_a_at 4.06293030342017
1552257_a_at 5.42169200934334
1552258_at 4.76014034386578
1552261_at 3.50486626185186
1552263_at 6.14921692323157
1552264_a_at 6.49242551292532
1552266_at 1.26646464160993

Total number of rows: 54675

Table truncated, full table size 1493 Kbytes.




Supplementary file Size Download File type/resource
GSM318887.CEL.gz 7.9 Mb (ftp)(http) CEL
Processed data included within Sample table

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