Semiautomated DNA probe mapping using digital imaging microscopy: I. System development

Laura N. Mascio, Piet W. Verbeek, Damir Sudar, Wen‐Lin ‐L Kuo, Joe W. Gray

Research output: Contribution to journalArticle

9 Scopus citations

Abstract

Algorithms have been developed to help automate the mapping of DNA sequences along metaphase chromosomes using fluorescence in situ hybridization (FISH). Custom algorithm computationally define chromosome boundaries and compute chromosomal medial axes. A dynamic regional thresholding (DRT) algorithm is described that allows reliable detection of hybridization domains, even when they differ substantially in size and intensity. Chromosomal locations are calculated by determining the fractional location of each hybridization probe along the medial axis of a metaphase chromosome relative to the short arm (FLpter). These algorithms were tested on simulated data and by analysis of the location of probes that had been previously mapped by other techniques. These algorithms allow probes to be mapped rapidly along human chromosomes with a precision of 2–3 Mb. © 1995 Wiley‐Liss, Inc.

Original languageEnglish (US)
Pages (from-to)51-59
Number of pages9
JournalCytometry
Volume19
Issue number1
DOIs
StatePublished - Jan 1 1995

Keywords

  • Segmentation
  • dynamic thresholding
  • feature extraction
  • fluorescence in situ hybridization
  • physical mapping

ASJC Scopus subject areas

  • Pathology and Forensic Medicine
  • Biophysics
  • Hematology
  • Endocrinology
  • Cell Biology

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