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Sample GSM5413223 Query DataSets for GSM5413223
Status Public on Jul 26, 2021
Title 1416_UC uninflamed sigmoid colon
Sample type RNA
 
Channel 1
Source name UC uninflamed sigmoid colon
Organism Homo sapiens
Characteristics Sex: not determined
diagnosis: Ulcerative colitis
inflammation: Uninflamed
tissue: Colon
batch: 7
Extracted molecule total RNA
Extraction protocol RNA was extracted with Qiagen RNeasy Plus kit with removal of genomic DNA.
Label Cy5
Label protocol Total RNA was converted to double-stranded cDNA and then into Cy-dye labeled cRNA using Quick Amp Labeling Kit (Agilent). For all samples, 750 ng of the labeled cRNA was fragmented and hybridized against Cy3-labeled Universal human reference (Stratagene, La Jolla, CA).
 
Channel 2
Source name Universal human reference (UHR) from Stratagene
Organism Homo sapiens
Characteristics sample type: pooled human reference RNA
Extracted molecule total RNA
Extraction protocol RNA was extracted with Qiagen RNeasy Plus kit with removal of genomic DNA.
Label Cy3
Label protocol Total RNA was converted to double-stranded cDNA and then into Cy-dye labeled cRNA using Quick Amp Labeling Kit (Agilent). For all samples, 750 ng of the labeled cRNA was fragmented and hybridized against Cy3-labeled Universal human reference (Stratagene, La Jolla, CA).
 
 
Hybridization protocol Agilent In Situ Hybridization Kit Plus was used where Cy-dye labeled control and test samples were applied to microarrays enclosed in Agilent SureHyb-enabled hybridization chambers. After hybridization, the arrays were washed twice, dried and then scanned.
Scan protocol Scanned on an Agilent scanner, images were processed using Agilent Feature Extraction software version 10.7.
Description SAM745532
Data processing Raw intensity data were background subtracted using the normal + exponential method from the limma Bioconductor package. The test/reference ratio was log2 transformed and normalized using loess normalization for each array. Loess normalized log2 ratios were then subjected to quantiles normalization across all arrays in the dataset.
 
Submission date Jul 01, 2021
Last update date Jul 27, 2021
Contact name Jason A Hackney
E-mail(s) hackney.jason@gene.com
Organization name Genentech, Inc.
Department Department of Bioinformatics and Computational Biology
Street address 1 DNA Way
City South San Francisco
State/province CA
ZIP/Postal code 94080
Country USA
 
Platform ID GPL6480
Series (1)
GSE179285 Embark cross-sectional study of inactive and active lesions from the ileum and colon of inflammatory bowel disease patients

Data table header descriptions
ID_REF
VALUE Normalized log2 ratio (test/reference)

Data table
ID_REF VALUE
A_24_P66027 1.506967765
A_32_P77178 0.968647639
A_23_P212522 1.402566742
A_24_P934473 0.906275797
A_24_P9671 0.529428547
A_32_P29551 2.040968614
A_24_P801451 0.727371635
A_32_P30710 1.012215772
A_32_P89523 1.050194264
A_24_P704878 1.058816275
A_32_P86028 0.827365476
A_24_P470079 0.917202603
A_23_P65830 0.993374081
A_23_P109143 0.274707136
A_24_P595567 0.92903815
A_24_P391591 0.851471391
A_24_P799245 0.928299759
A_24_P932757 0.996619929
A_24_P835500 1.38687883
A_23_P54340 0.983426598

Total number of rows: 41000

Table truncated, full table size 983 Kbytes.




Supplementary file Size Download File type/resource
GSM5413223_Agilent_251485060436_S01_GE2_107_Sep09_1_3.txt.gz 14.3 Mb (ftp)(http) TXT
Processed data included within Sample table

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