TY - JOUR
T1 - Estimating locations of quantum-dot-encoded microparticles from ultra-high density 3-D microarrays
AU - Sarder, Pinaki
AU - Nehorai, Arye
N1 - Funding Information:
Manuscript received March 10, 2008; revised June 05, 2008. Current version published February 06, 2009. This work was supported in part by the NSF under Grants CCR-0330342 and CCR-0630734, in part by the NIH under Grant 1T90 DA022871, and in part by the Mallinckrodt Institute of Radiology, Washington University. Asterisk indicates corresponding author. *P. Sarder is with the Department of Electrical and Systems Engineering, Washington University in St. Louis, St. Louis, MO 63130 USA (e-mail: [email protected]).
PY - 2008/12
Y1 - 2008/12
N2 - 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 Cramér-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.
AB - 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 Cramér-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.
KW - 3-D microarray
KW - Fluorescence microscope
KW - Maximum likelihood estimation
KW - Microparticle
KW - Q-dot
UR - https://www.scopus.com/pages/publications/60049090847
U2 - 10.1109/TNB.2008.2011861
DO - 10.1109/TNB.2008.2011861
M3 - Article
C2 - 19203872
AN - SCOPUS:60049090847
SN - 1536-1241
VL - 7
SP - 284
EP - 297
JO - IEEE Transactions on Nanobioscience
JF - IEEE Transactions on Nanobioscience
IS - 4
ER -