Literature DB >> 3941268

High-resolution image analysis.

K Preston.   

Abstract

In many departments of cytology, cytogenetics, hematology, and pathology, research projects using high-resolution computerized microscopy are now being mounted for computation of morphometric measurements on various structural components, as well as for determination of cellular DNA content. The majority of these measurements are made in a partially automated, computer-assisted mode, wherein there is strong interaction between the user and the computerized microscope. At the same time, full automation has been accomplished for both sample preparation and sample examination for clinical determination of the white blood cell differential count. At the time of writing, approximately 1,000 robot differential counting microscopes are in the field, analyzing images of human white blood cells, red blood cells, and platelets at the overall rate of about 100,000 slides per day. This mammoth through-put represents a major accomplishment in the application of machine vision to automated microscopy for hematology. In other areas of automated high-resolution microscopy, such as cytology and cytogenetics, no commercial instruments are available (although a few metaphase-finding machines are available and other new machines have been announced during the past year). This is a disappointing product, considering the nearly half century of research effort in these areas. This paper provides examples of the state of the art in automation of cell analysis for blood smears, cervical smears, and chromosome preparations. Also treated are new developments in multi-resolution automated microscopy, where images are now being generated and analyzed by a single machine over a range of 64:1 magnification and from 10,000 X 20,000 to 500 X 500 in total picture elements (pixels). Examples of images of human lymph node and liver tissue are presented. Semi-automated systems are not treated, although there is mention of recent research in the automation of tissue analysis.

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Year:  1986        PMID: 3941268     DOI: 10.1177/34.1.3941268

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  2 in total

1.  An automatic analysis method for in situ hybridization using high-resolution image analysis.

Authors:  W Stolz; K Scharffetter; W Abmayr; W Köditz; T Krieg
Journal:  Arch Dermatol Res       Date:  1989       Impact factor: 3.017

2.  Bright field microscopic cells counting method for BEVS using nonlinear convergence index sliding band filter.

Authors:  Dong Sui; Kuanquan Wang; Heemin Park; Jinseok Chae
Journal:  Biomed Eng Online       Date:  2014-10-24       Impact factor: 2.819

  2 in total

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