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Sample GSM2266924 Query DataSets for GSM2266924
Status Public on Aug 11, 2016
Title Data Heifer #10994_11v14
Sample type RNA
 
Channel 1
Source name Blasto_heifer_14
Organism Bos taurus
Characteristics sample type: in_vitro
developmental stage: early_blastocyst
breed (cattle): holstein
time of embryo collection: 168 hpf (hours post-in-vitro fertilization)
heifer age: 14 months
tissue or cell type: embryo
Treatment protocol Ovarian stimulation: Each heifer was first treated with progesterone (CIDR) during the luteal phase. The dominant follicle was aspirated 36 hours prior to administration of hormones. The ovarian stimulation program consisted of 6 injections of 30mg FSH ad
Embryo production: In vitro maturation (IVM), in vitro fertilization (IVF), in vitro culture (IVC)
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from the pools using the AllPrep DNA/RNA micro kit, following the Parallel gDNA and total RNA extraction protocol. Total RNA integrity and concentration were evaluated on an Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto
Amp protocol: To generate enough material for hybridization, the samples were linearly amplified. Antisense RNA (aRNA) was produced using the RiboAmp®HSPlus RNA Amplification kit (Thermo fisher Scientific). After two amplification rounds of 6 hr each, the
Label Cy5
Label protocol For each sample, aRNA was labeled using the ULS Fluorescent Labeling Kit for Agilent arrays (Cy3/Cy5) (Kreatech Diagnostics, Amsterdam, Netherlands). The labeled product was then purified with the Pico-Pure RNA Isolation Kit.
 
Channel 2
Source name Blasto_heifer_11
Organism Bos taurus
Characteristics sample type: in_vitro
developmental stage: early_blastocyst
breed (cattle): holstein
time of embryo collection: 168 hpf (hours post-in-vitro fertilization)
heifer age: 11 months
tissue or cell type: embryo
Treatment protocol Ovarian stimulation: Each heifer was first treated with progesterone (CIDR) during the luteal phase. The dominant follicle was aspirated 36 hours prior to administration of hormones. The ovarian stimulation program consisted of 6 injections of 30mg FSH ad
Embryo production: In vitro maturation (IVM), in vitro fertilization (IVF), in vitro culture (IVC)
Extracted molecule total RNA
Extraction protocol Total RNA was extracted from the pools using the AllPrep DNA/RNA micro kit, following the Parallel gDNA and total RNA extraction protocol. Total RNA integrity and concentration were evaluated on an Agilent 2100 Bioanalyzer (Agilent Technologies, Palo Alto
Amp protocol: To generate enough material for hybridization, the samples were linearly amplified. Antisense RNA (aRNA) was produced using the RiboAmp®HSPlus RNA Amplification kit (Thermo fisher Scientific). After two amplification rounds of 6 hr each, the
Label Cy3
Label protocol For each sample, aRNA was labeled using the ULS Fluorescent Labeling Kit for Agilent arrays (Cy3/Cy5) (Kreatech Diagnostics, Amsterdam, Netherlands). The labeled product was then purified with the Pico-Pure RNA Isolation Kit.
 
 
Hybridization protocol The hybridization of microarray slides 4x44K printed with oligonucleotides by Agilent for all EmbryoGENE related projects using the expression array protocol.
Scan protocol Scan on a PowerScanner (Tecan) using the autogain function. Images were quantified using ArrayPro version 6.3 (MediaCybernetics)
Description Rep 3 of 4
Data processing Background subtracted, Loess and Quantile normalized data obtained from log2 of processed Red signal/processed Green signal. Flexarray software used.
 
Submission date Aug 10, 2016
Last update date Aug 11, 2016
Contact name Léonie Morin-Doré
Organization name Laval University
Department Animal Sciences
Street address 2440, boulevard Hochelaga
City Quebec
State/province Quebec
ZIP/Postal code G1V 0A6
Country Canada
 
Platform ID GPL13226
Series (2)
GSE85437 Transcriptomic evaluation of bovine embryo quality on blastocysts obtained from peri-pubertal oocyte donors [11 mo vs 14 mo]
GSE85438 Transcriptomic evaluation of bovine embryo quality on blastocysts obtained from peri-pubertal oocyte donors

Data table header descriptions
ID_REF
VALUE Normalized log2 ratio (Cy3/Cy5) representing 11mo/14mo
INV_VALUE Normalized log2 ratio (Cy5/Cy3) representing 14mo/11mo

Data table
ID_REF VALUE INV_VALUE
EMBV3_00001 0.255415 -0.255414586
EMBV3_00002 -0.0401004 0.04010039
EMBV3_00003 -0.00635899 0.006358992
EMBV3_00004 0.154552 -0.154551763
EMBV3_00005 0.473535 -0.473534999
EMBV3_00006 -0.32638 0.326379634
EMBV3_00007 0.154209 -0.154208969
EMBV3_00008 -0.315232 0.315232299
EMBV3_00009 -0.0138655 0.013865478
EMBV3_00010 0.235697 -0.235696874
EMBV3_00011 0.00538698 -0.005386982
EMBV3_00012 -0.296548 0.296547748
EMBV3_00013 -0.226109 0.226108971
EMBV3_00014 -0.00487116 0.004871158
EMBV3_00015 0.526708 -0.526708108
EMBV3_00016 0.117308 -0.117308469
EMBV3_00017 -0.0365672 0.036567214
EMBV3_00018 -0.0294352 0.029435197
EMBV3_00019 -0.0360526 0.036052569
EMBV3_00020 0.820056 -0.820055575

Total number of rows: 43794

Table truncated, full table size 1455 Kbytes.




Supplementary file Size Download File type/resource
GSM2266924_data_lame_314_area3.txt.gz 1.8 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data are available on Series record

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