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Sample GSM138458 Query DataSets for GSM138458
Status Public on Oct 04, 2006
Title LDmuscle_CNgenotype_T0_rep2
Sample type RNA
 
Source name Longissimus dorsi (LD) muscle sample, Callipyge genotype (CN) at birth (T=0), technical rep2
Organism Ovis aries
Characteristics Genotype: CN (NCpat) paternal heterozygote
Age: T=0 birth
Treatment protocol Skeletal muscle samples were obtained from a flock of Dorset/Suffolk/Rambouillet cross-bred sheep raised at Utah State University. Matings were conducted to produce the genotypes for transcript profiling comparisons, particularly the genotypes NN and NCpat , where NN is the wild type and NCpat is the paternal heterozygote. The genotypes of all animals were confirmed using a genotyping test (Freking et al. 2002; Smit et al. 2003). Longissimus dorsi (LD) skeletal muscle samples were obtained from 8 male lambs representing four of each genotype, at birth (T0) and 11-12 weeks of age (T12). In addition, samples were also taken of semimembranosis (SM) and semitendonosis (ST) skeletal muscles from wild type lambs at 12 weeks of age. All muscles were carefully dissected out and weighed. Samples were then collected from each muscle at pre-determined sites. The samples were dissected from the animal within 15 minutes of euthanasia and immediately frozen under liquid nitrogen and stored at –80oC.
Growth protocol Animals were reared and euthanased in accordance with the animal ethics guidelines of Utah State University (Utah, USA)
Extracted molecule total RNA
Extraction protocol Trizol extraction of total RNA was performed according to the manufacturer's instructions.
Label biotin
Label protocol Biotinylated cRNA were prepared according to the standard Affymetrix protocol from 5 microg total RNA (Expression Analysis Technical Manual, 2001, Affymetrix).
 
Hybridization protocol Following fragmentation, 15 microg of cRNA were hybridized for 16 hr at 45C on GeneChip Bovine Genomer Array. GeneChips were washed and stained in the Affymetrix Fluidics Station 400.
Scan protocol GeneChips were scanned using the Affymetrix GeneChip Scanner 3000.
Description Gene expression data from the Callipyge genotype (CN) at birth (T=0) from muscle type (LD)
Data processing The data were analyzed with Microarray Suite version 5.0 (MAS 5.0) using Affymetrix default analysis settings and global scaling as normalization method. The trimmed mean target intensity of each array was arbitrarily set to 200.
 
Submission date Oct 03, 2006
Last update date Oct 03, 2006
Contact name Ross L Tellam
E-mail(s) Ross.Tellam@csiro.au
Phone 07 3214 2476
Organization name CSIRO Animal, Food and Health Sciences
Department Level 6 Queensland Biosciences Precinct
Lab University of Qld.
Street address 306 Carmody Road St.Lucia
City Brisbane
State/province QLD
ZIP/Postal code 4067
Country Australia
 
Platform ID GPL2112
Series (1)
GSE5955 Expression data from Callipyge muscle types (ST, LD, SS, SM) at birth (T=0) and 12 weeks (T=12)

Data table header descriptions
ID_REF
VALUE MAS5-calculated Signal intensity
ABS_CALL the call in an absolute analysis that indicates if the transcript was present (P), absent (A), marginal (M), or no call (NC)
DETECTION P-VALUE 'detection p-value', p-value that indicates the significance level of the detection call

Data table
ID_REF VALUE ABS_CALL DETECTION P-VALUE
AFFX-BioB-5_at 480.7 P 0.000095
AFFX-BioB-M_at 621 P 0.000044
AFFX-BioB-3_at 422.1 P 0.00007
AFFX-BioC-5_at 1651 P 0.000044
AFFX-BioC-3_at 1586.1 P 0.000052
AFFX-BioDn-5_at 2908.3 P 0.000044
AFFX-BioDn-3_at 6423.8 P 0.00006
AFFX-CreX-5_at 13404.2 P 0.000052
AFFX-CreX-3_at 18749.6 P 0.000044
AFFX-DapX-5_at 680.1 P 0.00006
AFFX-DapX-M_at 1050.5 P 0.000258
AFFX-DapX-3_at 1674.2 P 0.000052
AFFX-LysX-5_at 73.3 P 0.000195
AFFX-LysX-M_at 120.7 P 0.003212
AFFX-LysX-3_at 209.9 P 0.000147
AFFX-PheX-5_at 137.6 P 0.000147
AFFX-PheX-M_at 155.3 P 0.000446
AFFX-PheX-3_at 274.3 P 0.000195
AFFX-ThrX-5_at 229.2 P 0.00006
AFFX-ThrX-M_at 222.1 P 0.000044

Total number of rows: 24128

Table truncated, full table size 768 Kbytes.




Supplementary data files not provided

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