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Sample GSM1893772 Query DataSets for GSM1893772
Status Public on Dec 31, 2015
Title Subject_19_NONPREGNANT_Subcutaneous [gene-level]
Sample type RNA
 
Source name non pregnant_Subcutaneous
Organism Homo sapiens
Characteristics subject id: Subject 19
subject status: non pregnant
tissue: adipose
region: Subcutaneous
Treatment protocol No treatments were involved.
Growth protocol Paired visceral and subcutaneous adipose tissue samples were obtained after an eight-hour fast. Subcutaneous adipose tissue samples were collected at the site of a transverse lower abdominal incision, in the middle of the Pfannenstiel incision, from the deeper strata of subcutaneous fat. Visceral samples were obtained from the most distal portion of the greater omentum.(Visceral and subcutaneous adipose tissues were collected using Metzenbaum scissors and measured approximately 1.0 cm3. Tissues were snap-frozen in liquid nitrogen, and were kept at –80°C until use.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from snap-frozen adipose tissue samples using TRI Reagent® (Ambion®, Life Technologies Corporation, Austin, TX, USA) combined with the Qiagen RNeasy Lipid Tissue Kit protocol (Qiagen, Valencia, CA, USA), according to the manufacturers’ recommendations. The RNA concentrations and the A260 nm/A280 nm ratios were assessed using a NanoDrop® 1000 Spectrophotometer (Thermo Scientific, Wilmington, DE, USA). RNA integrity numbers were determined using the Agilent Bioanalyzer 2100 (Agilent Technologies, Wilmington, DE, USA).
Label biotin
Label protocol Standard Affymetrix Exon Array labeling protocol.
 
Hybridization protocol Standard Affymetrix Exon Array hyb protocol.
Scan protocol Standard Affymetrix Exon Array scan protocol.
Data processing Probe intensities were summarized and processed with RMA implemented in arroma.affymetrix package in R-3.2.2. For transcript level summaries ExonRmaPlm function from arroma.affymetrix was used (option mergeGroups=TRUE), while for probeset (exon) level summaries the option mergeGroups=FALSE was used.
probe group file: HuEx-1_0-st-v2.na30.hg19.probeset.csv
meta-probeset file: HuEx-1_0-st-v2.na30.hg19.transcript.csv
Log2 transformed probeset (exon) and transcript (group) level expression summaries for core transcripts based on NetAffx Nov. 12, 2007 (R3) (HuEx-1_0-st-v2,coreR3,A20071112,EP.cdf) .
 
Submission date Sep 25, 2015
Last update date Dec 31, 2015
Contact name Adi Tarca
E-mail(s) atarca@med.wayne.edu
Phone 3135775305
Organization name Wayne State University
Department Perinatology Research Branch (NIH/NICHD)
Street address 3990 John R
City Detroit
State/province MI
ZIP/Postal code 48188
Country USA
 
Platform ID GPL5175
Series (1)
GSE73439 Changes in gene expression and splicing associated with pregnancy, labor and regions of human adipose tissue.
Relations
Alternative to GSM1893874 (exon-level analysis)

Data table header descriptions
ID_REF
VALUE log2 normalized

Data table
ID_REF VALUE
2315251 5.287579798
2315373 6.828908721
2315554 7.960750737
2315633 7.690288545
2315674 7.515449485
2315739 7.682773036
2315894 8.337512475
2315918 6.439120816
2315951 7.286064879
2316069 8.347288302
2316218 6.426559351
2316245 6.743567977
2316379 9.684057174
2316558 8.010463226
2316605 7.227700104
2316746 8.146438937
2316905 6.526856549
2316953 7.260167532
2317246 7.144911029
2317317 7.513101558

Total number of rows: 18708

Table truncated, full table size 363 Kbytes.




Supplementary file Size Download File type/resource
GSM1893772_Sample_090.CEL.gz 24.1 Mb (ftp)(http) CEL
Processed data included within Sample table

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