Abstract:The physical (microtomy), optical (microscopy), and radiologic (tomography) sectioning of biological objects and their digitization lead to stacks of images. Due to the sectioning process and disturbances, movement of objects during imaging for example, adjacent images of the image stack are not optimally aligned to each other. Such mismatches have to be corrected automatically by suitable registration methods.Here, a whole brain of a Sprague Dawley rat was serially sectioned and stained followed by digitizing… Show more
“…Such techniques have for instance been applied to the evaluation of bone loss in ovariectomized animal models (Waarsing et al, 2006;Klinck et al, 2008). At the present, there are a number of different kinds of registration techniques (Brown 1992;van den Elsen et al, 1993;Modersitzki, 2004;Schmitt et al, 2007) for different registration problems, in particular for the alignment of images of serial sections. This includes e.g., rigid, affine and elastic registration.…”
Section: Biodegradation Of Porous Calcium Phosphate Scaffolds In An Ementioning
Three types of ceramic scaffolds with different composition and structure [namely synthetic 100% hydroxyapatite (HA; Engipore), synthetic calcium phosphate multiphase biomaterial containing 67% silicon stabilized tricalcium phosphate (Si-TCP; Skelite™) and natural bone mineral derived scaffolds (Bio-oss®)] were seeded with mesenchymal stem cells (MSC) and ectopically implanted for 8 and 16 weeks in immunodeficient mice. X-ray synchrotron radiation microtomography was used to derive 3D structural information on the same scaffolds both before and after implantation. Meaningful images and morphometric parameters such as scaffold and bone volume fraction, mean thickness and thickness distribution of the different phases as a function of the implantation time, were obtained. The used imaging algorithms allowed a direct comparison and registration of the 3D structure before and after implantation of the same sub-volume of a given scaffold. In this way it was possible to directly monitor the tissue engineered bone growth and the complete or partial degradation of the scaffold. Further, the detailed kinetics studies on Skelite™ scaffolds implanted for different length of times from 3 days to 24 weeks, revealed in the X-ray absorption histograms two separate peaks associated to HA and TCP. It was therefore possible to observe that the progressive degradation of the Skelite™ scaffolds was mainly due to the resorption of TCP. The different saturation times in the tissue engineered bone growth and in the TCP resorption confirmed that the bone growth was not limited the scaffold regions that were resorbed but continued in the inward direction with respect to the pore surface.
“…Such techniques have for instance been applied to the evaluation of bone loss in ovariectomized animal models (Waarsing et al, 2006;Klinck et al, 2008). At the present, there are a number of different kinds of registration techniques (Brown 1992;van den Elsen et al, 1993;Modersitzki, 2004;Schmitt et al, 2007) for different registration problems, in particular for the alignment of images of serial sections. This includes e.g., rigid, affine and elastic registration.…”
Section: Biodegradation Of Porous Calcium Phosphate Scaffolds In An Ementioning
Three types of ceramic scaffolds with different composition and structure [namely synthetic 100% hydroxyapatite (HA; Engipore), synthetic calcium phosphate multiphase biomaterial containing 67% silicon stabilized tricalcium phosphate (Si-TCP; Skelite™) and natural bone mineral derived scaffolds (Bio-oss®)] were seeded with mesenchymal stem cells (MSC) and ectopically implanted for 8 and 16 weeks in immunodeficient mice. X-ray synchrotron radiation microtomography was used to derive 3D structural information on the same scaffolds both before and after implantation. Meaningful images and morphometric parameters such as scaffold and bone volume fraction, mean thickness and thickness distribution of the different phases as a function of the implantation time, were obtained. The used imaging algorithms allowed a direct comparison and registration of the 3D structure before and after implantation of the same sub-volume of a given scaffold. In this way it was possible to directly monitor the tissue engineered bone growth and the complete or partial degradation of the scaffold. Further, the detailed kinetics studies on Skelite™ scaffolds implanted for different length of times from 3 days to 24 weeks, revealed in the X-ray absorption histograms two separate peaks associated to HA and TCP. It was therefore possible to observe that the progressive degradation of the Skelite™ scaffolds was mainly due to the resorption of TCP. The different saturation times in the tissue engineered bone growth and in the TCP resorption confirmed that the bone growth was not limited the scaffold regions that were resorbed but continued in the inward direction with respect to the pore surface.
“…Similar elastic constraints have been proposed earlier 9,10 , combining search for an elastic alignment and a pixel-based pairwise similarity estimate between adjacent sections in an iterative solution. They propose initial linear pre-alignment of the section series based on variants of principal component analysis.…”
Section: Supplementary Video 1 and Online Methods)mentioning
Anatomy of large biological specimens is often reconstructed from serially sectioned volumes imaged by high-resolution microscopy. We developed a method to reassemble a continuous volume from such large section series that explicitly minimizes artificial deformation by applying a global elastic constraint. We demonstrate our method on a series of transmission electron microscopy sections covering the entire 558-cell Caenorhabditis elegans embryo and a segment of the Drosophila melanogaster larval ventral nerve cord. DOI: https://doi.org/10. 1038/nmeth.2072 Posted at the Zurich Open Repository and Archive, University of Zurich ZORA URL: https://doi.org/10.5167/uzh-127852 Accepted Version Originally published at: Saalfeld, Stephan; Fetter, Richard; Cardona, Albert; Tomancak, Pavel (2012). Elastic volume reconstruction from series of ultra-thin microscopy sections. Nature Methods, 9(7):717-720. DOI: https://doi.org/10.1038/nmeth.2072
Elastic Volume Reconstruction from Series of Ultra-thin Microscopy SectionsStephan The downside of the method is that by physically cutting a block into sections the continuity between sections is lost and individual sections are deformed. To recover the imaged volume and extract biologically interesting information such as the reconstruction of neuronal circuits 2,3,5 , sections need to be aligned and distortion must be removed.Alignment can be achieved by maximizing the overlap of similar image content between adjacent sections. However, there are two unknowns that change image content across the section series: specimen's shape and independent section distortion introduced during preparation. Naively warping one section into another would compensate for the shape of the specimen and by that introduce artificial deformation. Our method exploits the fact that the biological specimen's shape typically changes smoothly across sections whereas the independent distortion in each section is random and uncorrelated with neighboring sections. We align all sections not only to their direct neighbors in the series but to all sections in a local neighborhood by modelling sections as two-dimensional elastic sheets that penalize non-rigid deformation ( Fig. 1a and Supplementary Fig. 1).All sections are treated as moving targets in a template-free global alignment. The elastic constraint is implemented as a spring-connected particle system where each section is represented as a triangular spring-mesh ( Fig. 1b and Supplementary Video 1 and Online methods).For each vertex of the spring-mesh, we search for the corresponding location in other sections by pairwise block-matching using normalized cross-correlation (NCC). To that end, we explore all translation vectors in an immediate neighborhood which requires sections to be in approximate alignment (Fig. 1c,d). We estimate this approximate alignment using automatically extracted landmark correspondences from invariant local image features as described previously 7,8 . Originally proposed for robust object recognition under partial occlus...
“…Large scale image registration has many applications in both biomedical research [10,22,32] and geophysics [33]. However, there are currently few works addressing image registration algorithms intended to run efficiently on high performance computing environments.…”
Section: Related Workmentioning
confidence: 99%
“…The work on parallel image registration on multicomputers is limited [22] and is restricted to either large computer clusters [34][35][36] or IBM cell clusters [37]. Clusters of GPUs have been used to implement other heavy workload tasks [38], mostly within the simulation and visualization fields.…”
Microscopic imaging is an important tool for characterizing tissue morphology and pathology. 3D reconstruction and visualization of large sample tissue structure requires registration of large sets of high-resolution images. However, the scale of this problem presents a challenge for automatic registration methods. In this paper we present a novel method for efficient automatic registration using graphics processing units (GPUs) and parallel programming. Comparing a C++ CPU implementation with Compute Unified Device Architecture (CUDA) libraries and pthreads running on GPU we achieve a speed-up factor of up to 4.11× with a single GPU and 6.68× with a GPU pair. We present execution times for a benchmark composed of two sets of large-scale images: mouse placenta (16K × 16K pixels) and breast cancer tumors (23K × 62K pixels). It takes more than 12 hours for the genetic case in C++ to register a typical sample composed of 500 consecutive slides, which was reduced to less than 2 hours using two GPUs, in addition to a very promising scalability for extending those gains easily on a large number of GPUs in a distributed system.
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