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Vector algebra in the analysis of genome-wide expression data 英文参考文献
/2002/3/3/research/0011.1
Research
Vector algebra in the analysis of genome-wide expression data
inny G Kuruvilla*, Peter J Park? and Stuart L Schreiber*
Addresses: *Howard Hughes Medical Institute, Bauer Center for Genomics Research, Department of Chemistry and Chemical Biology,
Harvard University, Cambridge, MA 02138, USA. ?Department of Biostatistics, Harvard School of Public Health, Informatics Program,
Children?s Hospital, Harvard Medical School, Boston, MA 02115, USA.
Correspondence: Stuart L Schreiber. E-mail: sls@
Published: 13 February 2002
Received: 20 August 2001
Revised: 14 December 2001
Accepted: 11 January 2002
GenomeBiology 2002, 3(3):research0011.1–0011.11
The electronic version of this article is the complete one and can be
found online at /2002/3/3/research/0011
? 2002 Kuruvilla et al., licensee BioMed Central Ltd
(Print ISSN 1465-6906; Online ISSN 1465-6914)
Abstract
Background: Data from thousands of transcription-profiling experiments in organisms ranging
from yeast to humans are now publicly available. How best to analyze these data remains an
important challenge. A variety of tools have been used for this purpose, including hierarchical
clustering, self-organizing maps and principal components analysis. In particular, concepts from
vector algebra have proven useful in the study of genome-wide expression data.
Results: Here we present a framework based on vector algebra for the analysis of transcription
profiles that is geometrically intuitive and computationally efficient. Concepts in vector algebra such
as angles, magnitudes, subspaces, singular value decomposition, bases and projections have natural
and powerful interpretations in the analysis of microarray data. Angles in particular offer a rigorous
method of defining ‘similarity’ and are useful in evaluating the claims of a microarray-based study.
We present a sample analysis of cells treated with rapamycin, an immunosuppressant who
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