Genome Research

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplemental Research Data
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Theilhaber, J.
Right arrow Articles by Baron, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Theilhaber, J.
Right arrow Articles by Baron, R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

Vol. 12, Issue 1, 165-176, January 2002

METHODS
Finding Genes in the C2C12 Osteogenic Pathway by k-Nearest-Neighbor Classification of Expression Data

Joachim Theilhaber,1,4 Timothy Connolly,1 Sergio Roman-Roman,2 Steven Bushnell,1 Amanda Jackson,3 Kathy Call,1 Teresa Garcia,2 and Roland Baron2

1 Aventis Pharmaceuticals, Cambridge Genomics Center, Cambridge, Massachusetts 02139, USA; 2 Aventis Pharmaceuticals, Bone Disease Group, 93235 Romainville, France; 3 CuraGen Corporation, New Haven, Connecticut 06511, USA

A supervised classification scheme for analyzing microarray expression data, based on the k-nearest-neighbor method coupled to noise-reduction filters, has been used to find genes involved in the osteogenic pathway of the mouse C2C12 cell line studied here as a model for in vivo osteogenesis. The scheme uses as input a training set embodying expert biological knowledge, and provides internal estimates of its own misclassification errors, which furthermore enables systematic optimization of the classifier parameters. On the basis of the C2C12-generated expression data set with 34,130 expression profiles across 2 time courses, each comprised of 6 points, and a training set containing known members of the osteogenic, myoblastic, and adipocytic pathways, 176 new genes in addition to 28 originally in the training set are selected as relevant to osteogenesis. For this selection, the estimated sensitivity is 42% and the posterior false-positive rate (fraction of candidates that are spurious) is 12%. The corresponding sensitivity and false-positive rate for detection of myoblastic genes are 9% and 31%, respectively, and only 4% and ~100%, respectively, for adipocytic genes, in accordance with an experimental design that predominantly stimulated the osteogenic pathway. Validation of this selection is provided by examining expression of the genes in an independent biological assay involving mouse calvaria (skull bone) primary cell cultures, in which a large fraction of the 176 genes are seen to be strongly regulated, as well as by case-by-case analysis of the genes on the basis of expert domain knowledge. The methodology should be generalizable to any situation in which enough a priori biological knowledge exists to define a training set.

[Online supplementary material available at www.genome.org]


4 Corresponding author.


12:165-176 ©2002 by Cold Spring Harbor Laboratory Press  ISSN 1088-9051/02 $5.00

Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
D. Fan, Z. Chen, Y. Chen, and Y. Shang
Mechanistic Roles of Leptin in Osteogenic Stimulation in Thoracic Ligament Flavum Cells
J. Biol. Chem., October 12, 2007; 282(41): 29958 - 29966.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
T. W. Chittenden, J. A. Sherman, F. Xiong, A. E. Hall, A. A. Lanahan, J. M. Taylor, H. Duan, J. D. Pearlman, J. H. Moore, S. M. Schwartz, et al.
Transcriptional Profiling in Coronary Artery Disease: Indications for Novel Markers of Coronary Collateralization
Circulation, October 24, 2006; 114(17): 1811 - 1820.
[Abstract] [Full Text] [PDF]


Home page
CarcinogenesisHome page
M. M. Chan, X. Lu, F. M. Merchant, J.D. Iglehart, and P. L. Miron
Gene expression profiling of NMU-induced rat mammary tumors: cross species comparison with human breast cancer
Carcinogenesis, August 1, 2005; 26(8): 1343 - 1353.
[Abstract] [Full Text] [PDF]


Home page
Physiol. GenomicsHome page
P. G. Giresi, E. J. Stevenson, J. Theilhaber, A. Koncarevic, J. Parkington, R. A. Fielding, and S. C. Kandarian
Identification of a molecular signature of sarcopenia
Physiol Genomics, April 14, 2005; 21(2): 253 - 263.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
S. Roman-Roman, D.-L. Shi, V. Stiot, E. Hay, B. Vayssiere, T. Garcia, R. Baron, and G. Rawadi
Murine Frizzled-1 Behaves as an Antagonist of the Canonical Wnt/{beta}-Catenin Signaling
J. Biol. Chem., February 13, 2004; 279(7): 5725 - 5733.
[Abstract] [Full Text] [PDF]


Home page
Adv. Dent. Res.Home page
W.P. Kuo
Overview of Bioinformatics and its Application to Oral Genomics
Adv. Dent. Res., December 1, 2003; 17(1): 89 - 94.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
Genes Dev. Learn. Mem.
Protein Science RNA Genome Res.