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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

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