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Sample GSM2203131 Query DataSets for GSM2203131
Status Public on Jun 08, 2020
Title Crohn's_Disease__patient11
Sample type RNA
 
Source name intestinal mucosa
Organism Homo sapiens
Characteristics tissue: intestinal mucosa
inflammation: Inflamed margin
Extracted molecule total RNA
Extraction protocol Total RNA, including small RNA, from ileocolectomy samples was insolated using RNAeasy® Mini Kit extraction (QIAGEN Inc., CA, USA) following manufacturer's instructions. The samples were previously stabilizaded with RNAlater reagent during 24h. RNA quality and integrity were analyzed by Experion bioanalyzer (Bio-Rad, CA, USA).
Label Biotin
Label protocol Total RNA (1μg) was primed for reverse transcription with oligo-dT primer containing the T7 RNA polymerase promoter site. After second-strand cDNA synthesis, the dscDNA served as the template for an in vitro transcription (IVT) reaction to produce the target cRNA. IVT was performed by the linear amplification method in the presence of biotin-modified UTP to label the target cRNA. MessageAmp TM II-Biotin Enhanced kit was used (Ambion, Ma, USA).
 
Hybridization protocol Biotin labeled cRNA (10ug) was hybridized on CodeLink™ Human Whole Genome Bioarray overnight at 37°C (Applied Microarrays, AZ, USA). Labeling with Cy5-streptavidin was performed.
Scan protocol Scanning was performed on InnoScan® 700 microarray scanner and Mapix Software (ArrayIt Corporation, CA, USA)
Description RNA extracted from an instestinal biopsy of a CD patient
Data processing Raw data include raw intensity values from all gene expression microarray probes (n=56,448 probes, Platform GPL2895). Non-normalized data include intensity values on the log2 scale for a total of 20,902 probes that passed the quality control analysis (Probes with RefSeq annotation -April 2015- and mapping to a single gene). Log2 transformation of GE Healthcare/Amersham Biosciences CodeLink Human Whole Genome Bioarray raw data, RefSeq probe annotation update (16th April, 2015), quantile normalization and batch effect adjustment using the preprocessCore and Combat R packages, respectively.
 
Submission date Jun 16, 2016
Last update date Jun 08, 2020
Contact name Adrià Aterido
E-mail(s) adria.aterido@vhir.org
Phone +34 934029082
Organization name Vall d'Hebron Hospital Research Institute
Department Rheumatology Research Group
Lab Rheumatology Research Group
Street address c/ Baldiri Reixac nº15
City Barcelona
State/province Barcelona
ZIP/Postal code 08028
Country Spain
 
Platform ID GPL18134
Series (1)
GSE83448 Genome-wide transcriptional analysis in intestinal biopsies from Crohn's disease (CD) patients.

Data table header descriptions
ID_REF
VALUE Quantile normalization.

Data table
ID_REF VALUE
GE81638 12.89931643
GE895719 9.612548938
GE79164 15.71562881
GE509900 10.58195834
GE59292 10.33743054
GE59708 11.54569583
GE53205 15.44210298
GE53426 12.78229587
GE82609 15.20616693
GE79286 11.49803842
GE58747 8.088946906
GE58973 14.85950082
GE544889 9.664724579
GE53177 11.09671883
GE55366 11.05150955
GE57831 14.93215734
GE58021 15.37452375
GE787583 9.634737681
GE88819 15.44934898
GE87069 14.8138342

Total number of rows: 20902

Table truncated, full table size 411 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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