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Sample GSM1893794 Query DataSets for GSM1893794
Status Public on Dec 31, 2015
Title Subject_35_NONPREGNANT_Subcutaneous [gene-level]
Sample type RNA
 
Source name non pregnant_Subcutaneous
Organism Homo sapiens
Characteristics subject id: Subject 35
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 GSM1893896 (exon-level analysis)

Data table header descriptions
ID_REF
VALUE log2 normalized

Data table
ID_REF VALUE
2315251 5.409437553
2315373 6.80091451
2315554 8.135042105
2315633 7.821920798
2315674 7.703174348
2315739 7.769666262
2315894 8.83229098
2315918 7.020644629
2315951 7.675798891
2316069 8.402123395
2316218 6.727139585
2316245 7.057389419
2316379 9.860387693
2316558 8.225718022
2316605 7.48924149
2316746 8.35337085
2316905 6.739985027
2316953 7.330668279
2317246 7.329298984
2317317 7.72373374

Total number of rows: 18708

Table truncated, full table size 363 Kbytes.




Supplementary file Size Download File type/resource
GSM1893794_Sample_117.CEL.gz 22.7 Mb (ftp)(http) CEL
Processed data included within Sample table

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