NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM2647998 Query DataSets for GSM2647998
Status Public on Dec 25, 2018
Title C3H control d21 #1, batch E
Sample type RNA
 
Source name Femur bone following experimental fracture
Organism Mus musculus
Characteristics tissue: bone fracture callus
gender: male
batch: batch E
strain: C3H
diet: control
timepoint: day 21
animal: 1079
Treatment protocol Pi group: Phosphate deficiency (Pi) was initiated 2 days prior to fracture and was maintained for 15 days by supplying the mice with a low phosphate diet (Harlan Laboratories, Madison, WI). Phosphate was then replenished and bone healing was allowed to continue until 35 days. For the three strains of mice, control groups were included where the mice were given normal diet throughout the study.
Growth protocol In vivo animal model
Extracted molecule total RNA
Extraction protocol Total RNAs were isolated from each fracture callus using procedures developed for murine bones (Wang et al., Matrix Biology, 2006; 25(5):271-81). In order to both achieve an optimal balance in biological replicate variability and repeatability RNA from every two of the six fracture calluses were randomly pooled to generate three assay samples.
Label biotin
Label protocol Biotin labeling was performed using the Ambion WT Expression Kit (Life Technologies, Grand Island, NY) according to the manufacturer's protocol, followed by the GeneChip WT Terminal Labeling and Controls Kit (Affymetrix, Santa Clara, CA).
 
Hybridization protocol The labeled, fragmented DNA was hybridized to the Affymetrix Mouse Gene 1.0 ST Array for 18 hours in a GeneChip Hybridization oven 640 at 45oC with rotation (60 rpm). The hybridized samples were washed and stained using an Affymetrix fluidics station 450.
Scan protocol After staining, microarrays were immediately scanned using an Affymetrix GeneArray Scanner 3000 7G Plus.
Description Gene expression data from right femur of C3H control animal at day 21 following experimental fracture.
Data processing Raw Affymetrix CEL files were normalized to produce Entrez Gene-identifier-specific expression values using the implementation of the Robust Multiarray Average (RMA) in the affy Bioconductor package (version 1.36.1), using R version 2.15.1 and the Brainarray mogene10stmmentrezg R package (version 16.0.0).
 
Submission date Jun 01, 2017
Last update date Jun 25, 2019
Contact name Boston University Microarray and Sequencing Resource
E-mail(s) [email protected]
Organization name Boston University
Department Microarray and Sequencing Resource
Street address 72 East Concord Street, E631
City Boston
State/province MA
ZIP/Postal code 02118
Country USA
 
Platform ID GPL19485
Series (1)
GSE99580 A Systems Genetics Approach to Fracture Healing

Data table header descriptions
ID_REF
VALUE log2-transformed, RMA-normalized Entrez Gene expression values

Data table
ID_REF VALUE
100008567_at 5.561810429
100009600_at 4.66570007
100009609_at 2.412103684
100009614_at 5.17173482
100012_at 3.404095841
100017_at 8.564903703
100019_at 6.912840926
100033459_at 3.675716099
100034251_at 7.417150022
100034748_at 4.894214617
100036520_at 4.864021014
100036521_at 6.337403935
100036523_at 6.112879666
100036537_at 5.457654034
100036768_at 4.501583555
100037258_at 9.404273479
100037260_at 5.736859309
100037262_at 5.663049327
100037278_at 7.912102047
100037396_at 5.002544851

Total number of rows: 21187

Table truncated, full table size 442 Kbytes.




Supplementary file Size Download File type/resource
GSM2647998_2014-07-28_LG_C5_1079.CEL.gz 3.7 Mb (ftp)(http) CEL
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap