Title :
Estimating Locations of Quantum-Dot-Encoded Microparticles From Ultra-High Density 3-D Microarrays
Author :
Sarder, Pinaki ; Nehorai, Arye
Author_Institution :
Dept. of Electr. & Syst. Eng., Washington Univ. in St. Louis, St. Louis, MO, USA
Abstract :
We develop a maximum likelihood (ML)-based parametric image deconvolution technique to locate quantum-dot (q-dot) encoded microparticles from three-dimensional (3-D) images of an ultra-high density 3-D microarray. A potential application of the proposed microarray imaging is assay analysis of gene, protein, antigen, and antibody targets. This imaging is performed using a wide-field fluorescence microscope. We first describe our problem of interest and the pertinent measurement model by assuming additive Gaussian noise. We use a 3-D Gaussian point-spread-function (PSF) model to represent the blurring of the widefield microscope system. We employ parametric spheres to represent the light intensity profiles of the q-dot-encoded microparticles. We then develop the estimation algorithm for the single-sphere-object image assuming that the microscope PSF is totally unknown. The algorithm is tested numerically and compared with the analytical Cramer-Rao bounds (CRB). To apply our analysis to real data, we first segment a section of the blurred 3-D image of the multiple microparticles using a k-means clustering algorithm, obtaining 3-D images of single-sphere-objects. Then, we process each of these images using our proposed estimation technique. In the numerical examples, our method outperforms the blind deconvolution (BD) algorithms in high signal-to-noise ratio (SNR) images. For the case of real data, our method and the BD-based methods perform similarly for the well-separated microparticle images.
Keywords :
biological techniques; deconvolution; fluorescence; image denoising; image restoration; maximum likelihood estimation; optical microscopy; optical transfer function; quantum dots; 3D Gaussian PSF model; Cramer-Rao bounds; additive Gaussian noise; antibody assay analysis; antigen assay analysis; gene assay analysis; k-means clustering algorithm; maximum likelihood method; microarray imaging; parametric image deconvolution technique; parametric spheres; point spread function; protein assay analysis; q-dot encoded microparticle localisation; quantum dot encoded microparticles; single sphere object image; ultrahigh density 3D microarrays; wide field fluorescence microscope; widefield microscope system blurring; Algorithm design and analysis; Clustering algorithms; Deconvolution; Fluorescence; Image analysis; Maximum likelihood estimation; Microscopy; Noise measurement; Proteins; Quantum dots; 3-D microarray; Fluorescence microscope; maximum likelihood estimation; microparticle; q-dot; Algorithms; Equipment Design; Equipment Failure Analysis; Image Interpretation, Computer-Assisted; Imaging, Three-Dimensional; Microarray Analysis; Microscopy, Fluorescence; Microspheres; Quantum Dots;
Journal_Title :
NanoBioscience, IEEE Transactions on
DOI :
10.1109/TNB.2008.2011861