Deconvolving cell cycle expression data with complementary information

Bioinformatics. 2004 Aug 4:20 Suppl 1:i23-30. doi: 10.1093/bioinformatics/bth915.

Abstract

Motivation: In the study of many systems, cells are first synchronized so that a large population of cells exhibit similar behavior. While synchronization can usually be achieved for a short duration, after a while cells begin to lose their synchronization. Synchronization loss is a continuous process and so the observed value in a population of cells for a gene at time t is actually a convolution of its values in an interval around t. Deconvolving the observed values from a mixed population will allow us to obtain better models for these systems and to accurately detect the genes that participate in these systems.

Results: We present an algorithm which combines budding index and gene expression data to deconvolve expression profiles. Using the budding index data we first fit a synchronization loss model for the cell cycle system. Our deconvolution algorithm uses this loss model and can also use information from co-expressed genes, making it more robust against noise and missing values. Using expression and budding data for yeast we show that our algorithm is able to reconstruct a more accurate representation when compared with the observed values. In addition, using the deconvolved profiles we are able to correctly identify 15% more cycling genes when compared to a set identified using the observed values.

Availability: Matlab implementation can be downloaded from the supporting website http://www.cs.cmu.edu/~zivbj/decon/decon.html

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Biological Clocks / physiology*
  • Cell Communication / physiology
  • Cell Cycle / physiology*
  • Cell Cycle Proteins / metabolism*
  • Computer Simulation
  • Databases, Protein
  • Gene Expression Profiling / methods
  • Gene Expression Regulation / physiology
  • Models, Biological*
  • Saccharomycetales / cytology*
  • Saccharomycetales / physiology*

Substances

  • Cell Cycle Proteins