TY - GEN
T1 - A new approach for 3D segmentation of cellular tomograms obtained using three-dimensional electron microscopy
AU - Bartesaghi, A.
AU - Sapiro, G.
AU - Lee, S.
AU - Lefman, J.
AU - Wahl, S.
AU - Orenstein, J.
AU - Subramaniam, S.
PY - 2004
Y1 - 2004
N2 - Electron tomography allows determination of the three-dimensional structures of cells and tissues at resolutions significantly higher than is possible with optical microscopy. Electron tomograms contain, in principle, vast amounts of information on the locations and architectures of large numbers of subcellular assemblies and organelles. The development of reliable quantitative approaches for interpretation of features in tomograms, is an important problem, but is a challenging prospect because of the low signal-to-noise ratios that are inherent to biological electron microscopic images. As a first step in this direction, we report methods for the automated statistical analysis of HIV particles and selected cellular compartments in electron tomograms recorded from fixed, plastic-embedded sections derived from HIV-infected human macrophages. Individual features in the tomogram are segmented using a novel, robust algorithm that finds their boundaries as global minimal surfaces in a metric space defined by image features. Our expectation is that such methods will provide tools for semi-automated detection and statistical evaluation of HIV particles at different stages of assembly in the cells, and present opportunities for correlation with biochemical markers of HIV infection.
AB - Electron tomography allows determination of the three-dimensional structures of cells and tissues at resolutions significantly higher than is possible with optical microscopy. Electron tomograms contain, in principle, vast amounts of information on the locations and architectures of large numbers of subcellular assemblies and organelles. The development of reliable quantitative approaches for interpretation of features in tomograms, is an important problem, but is a challenging prospect because of the low signal-to-noise ratios that are inherent to biological electron microscopic images. As a first step in this direction, we report methods for the automated statistical analysis of HIV particles and selected cellular compartments in electron tomograms recorded from fixed, plastic-embedded sections derived from HIV-infected human macrophages. Individual features in the tomogram are segmented using a novel, robust algorithm that finds their boundaries as global minimal surfaces in a metric space defined by image features. Our expectation is that such methods will provide tools for semi-automated detection and statistical evaluation of HIV particles at different stages of assembly in the cells, and present opportunities for correlation with biochemical markers of HIV infection.
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M3 - Conference contribution
AN - SCOPUS:17144383648
SN - 0780383885
SN - 9780780383883
T3 - 2004 2nd IEEE International Symposium on Biomedical Imaging: Macro to Nano
SP - 5
EP - 8
BT - 2004 2nd IEEE International Symposium on Biomedical Imaging
T2 - 2004 2nd IEEE International Symposium on Biomedical Imaging: Macro to Nano
Y2 - 15 April 2004 through 18 April 2004
ER -