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Sample GSM1277325 Query DataSets for GSM1277325
Status Public on Dec 04, 2013
Title BL6_T5-135_1d_heart
Sample type RNA
 
Source name Stressed_heart_tissue, T5R1
Organism Mus musculus
Characteristics strain: C57BL/6
tissue: Stressed_heart_tissue, T5R1
Treatment protocol The experimental animals were kept in a wire mesh box inside the aggressor´s cage for 6 hours a day for either 5 or 10 consecutive days. Animals were randomly assigned to aggressors cages. Each subject mouse was randomly placed 3-5 times within the home cage of an aggressor mouse and received bites/attacks for up to 2 min (or until 10 attacks/bites occurred, whichever came first. Each day the stress procedure occurred at different times and different resident mice were used for each aggressor. Body weight and temperature of the experimental mice were measured every day prior the beginning of the social defeat period and the return to their home cages. Control mice were kept inside of the wired mesh boxes inside of a large cage without any aggressor.
Extracted molecule total RNA
Extraction protocol Total RNA was isolated from individual mouse heart samples by homogenization in TRIzol reagent per the manufacturer’s protocol (Invitrogen, Gran Island, NY). The quality and quantity of the RNA samples were evaluated using a NanoDrop ND-1000 spectrophotometer (Thermo Scientific, Waltham, MA) and Agilent 2100 BioAnalyzer (Agilent, Santa Clara, CA).
Label Hy3
Label protocol Total RNA from the heart tissue was labeled with either Hy3 or Hy5 dye with labeling kits from Exiqon then hybridized at 56°C for 16 h.
 
Hybridization protocol Labeled samples were hybridized to Exiqon 5th generation miRCURY LNA microRNA array according to the manufacturer's protocol.
Scan protocol After hybridization, the slides were washed and scanned with a scanner from Agilent (Santa Clara, CA).
Description BL6_T5-135_1d_heart_miRNA_Hy3_v_BL6_T5-137_1d_heart_miRNA_Hy5.csv
Data processing Scanned data was processed using AnalyzerDG software. For the preprocessing of two-channel microarray data in each experimental group, Hy3 and Hy5 (high energy scanned) intensities were concatenated, normalized using LOWESS (within-array normalization) and normalized using the quantile method (between-array normalization).
 
Submission date Dec 02, 2013
Last update date Dec 04, 2013
Contact name Ji-Hoon Cho
E-mail(s) [email protected]
Organization name Institute for Systems Biology
Street address 401 Terry Avenue North
City Seattle
State/province WA
ZIP/Postal code 98109
Country USA
 
Platform ID GPL11432
Series (2)
GSE52869 miRNA expression signatures in heart tissues of mice simulating posttraumatic stress disorder (PTSD) [Study1]
GSE52875 Expression signatures in heart tissues of mice simulating posttraumatic stress disorder (PTSD)

Data table header descriptions
ID_REF
VALUE Since there are four identical replicated probes for each miRNA in the Exiqon microarray platform, they were consolidated by taking the median expression value over the replicated probes to remove redundancy.

Data table
ID_REF VALUE
-1 5.925367554
1100 9.331847773
4040 5.675898591
4390 6.044092461
4610 9.499579529
4700 5.200829729
5250 5.654989253
5730 7.74436234
5740 7.872627917
6880 5.689662756
9938 7.509574313
10138 6.624088549
10306 5.771539152
10899 5.24449944
10901 5.010613381
10902 5.177323252
10903 5.150001265
10904 5.138551777
10905 5.16476103
10906 5.470084847

Total number of rows: 2025

Table truncated, full table size 35 Kbytes.




Supplementary data files not provided
Processed data included within Sample table

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