Optimization of probe coverage for high-resolution oligonucleotide aCGH

Bioinformatics. 2007 Jan 15;23(2):e77-83. doi: 10.1093/bioinformatics/btl316.

Abstract

Motivation: The resolution at which genomic alterations can be mapped by means of oligonucleotide aCGH (array-based comparative genomic hybridization) is limited by two factors: the availability of high-quality probes for the target genomic sequence and the array real-estate. Optimization of the probe selection process is required for arrays that are designed to probe specific genomic regions in very high resolution without compromising probe quality constraints.

Results: In this paper we describe a well-defined optimization problem associated with the problem of probe selection for high-resolution aCGH arrays. We propose the whenever possible in-cover as a formulation that faithfully captures the requirement of probe selection problem, and provide a fast randomized algorithm that solves the optimization problem in O(n logn) time, as well as a deterministic algorithm with the same asymptotic performance. We apply the method in a typical high-definition array design scenario and demonstrate its superiority with respect to alternative approaches.

Availability: Address requests to the authors.

MeSH terms

  • Base Sequence
  • Chromosome Mapping / methods*
  • DNA Probes / genetics*
  • Gene Dosage / genetics*
  • In Situ Hybridization, Fluorescence / methods*
  • Molecular Sequence Data
  • Oligonucleotide Array Sequence Analysis / methods*
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Sequence Alignment / methods*
  • Sequence Analysis, DNA / methods*

Substances

  • DNA Probes