Literature DB >> 23410911

A motion correction framework for time series sequences in microscopy images.

Ankur N Kumar1, Kurt W Short, David W Piston.   

Abstract

With the advent of in vivo laser scanning fluorescence microscopy techniques, time-series and three-dimensional volumes of living tissue and vessels at micron scales can be acquired to firmly analyze vessel architecture and blood flow. Analysis of a large number of image stacks to extract architecture and track blood flow manually is cumbersome and prone to observer bias. Thus, an automated framework to accomplish these analytical tasks is imperative. The first initiative toward such a framework is to compensate for motion artifacts manifest in these microscopy images. Motion artifacts in in vivo microscopy images are caused by respiratory motion, heart beats, and other motions from the specimen. Consequently, the amount of motion present in these images can be large and hinders further analysis of these images. In this article, an algorithmic framework for the correction of time-series images is presented. The automated algorithm is comprised of a rigid and a nonrigid registration step based on shape contexts. The framework performs considerably well on time-series image sequences of the islets of Langerhans and provides for the pivotal step of motion correction in the further automatic analysis of microscopy images.

Entities:  

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Year:  2013        PMID: 23410911      PMCID: PMC4135398          DOI: 10.1017/S1431927612014250

Source DB:  PubMed          Journal:  Microsc Microanal        ISSN: 1431-9276            Impact factor:   4.127


  19 in total

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2.  Background rejection and signal-to-noise optimization in confocal and alternative fluorescence microscopes.

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Journal:  Appl Opt       Date:  1994-02-01       Impact factor: 1.980

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Authors:  Greg Mori; Serge Belongie; Jitendra Malik
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Authors:  E Dusch; T Dorval; N Vincent; M Wachsmuth; A Genovesio
Journal:  J Microsc       Date:  2007-11       Impact factor: 1.758

Review 6.  Pancreas islets in metabolic signaling--focus on the beta-cell.

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Journal:  Front Biosci       Date:  2008-05-01

7.  Nonrigid registration of 3-d multichannel microscopy images of cell nuclei.

Authors:  S Yang; D Kohler; K Teller; T Cremer; P Le Baccon; E Heard; R Eils; K Rohr
Journal:  IEEE Trans Image Process       Date:  2008-04       Impact factor: 10.856

8.  Contrast limited adaptive histogram equalization image processing to improve the detection of simulated spiculations in dense mammograms.

Authors:  E D Pisano; S Zong; B M Hemminger; M DeLuca; R E Johnston; K Muller; M P Braeuning; S M Pizer
Journal:  J Digit Imaging       Date:  1998-11       Impact factor: 4.056

9.  The GluCre-ROSA26EYFP mouse: a new model for easy identification of living pancreatic alpha-cells.

Authors:  Nicolas Quoix; Rui Cheng-Xue; Yves Guiot; Pedro L Herrera; Jean-Claude Henquin; Patrick Gilon
Journal:  FEBS Lett       Date:  2007-08-07       Impact factor: 4.124

10.  Motion correction for phase-resolved dynamic optical coherence tomography imaging of rodent cerebral cortex.

Authors:  Jonghwan Lee; Vivek Srinivasan; Harsha Radhakrishnan; David A Boas
Journal:  Opt Express       Date:  2011-10-24       Impact factor: 3.894

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  3 in total

1.  Connexin 36 mediates blood cell flow in mouse pancreatic islets.

Authors:  Kurt W Short; W Steve Head; David W Piston
Journal:  Am J Physiol Endocrinol Metab       Date:  2013-12-10       Impact factor: 4.310

2.  IMART software for correction of motion artifacts in images collected in intravital microscopy.

Authors:  Kenneth W Dunn; Kevin S Lorenz; Paul Salama; Edward J Delp
Journal:  Intravital       Date:  2014

Review 3.  Multiphoton intravital microscopy in small animals: motion artefact challenges and technical solutions.

Authors:  D Soulet; J Lamontagne-Proulx; B Aubé; D Davalos
Journal:  J Microsc       Date:  2020-03-05       Impact factor: 1.758

  3 in total

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