TY - JOUR
T1 - Estimating gene signals from noisy microarray images
AU - Sarder, Pinaki
AU - Nehorai, Arye
AU - Davis, Paul H.
AU - Stanley, Samuel L.
N1 - Funding Information:
Manuscript received November 5, 2007; revised January 31, 2008. 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]). A. Nehorai is with the Department of Electrical and Systems Engineering, Washington University in St. Louis, St. Louis, MO 63130, USA (fax: (314) 935-7500, e-mail: [email protected]). P. H. Davis is with the Department of Biology, University of Pennsylvania, Philadelpha, PA 19104 USA (e-mail: [email protected]). S. L. Stanley, Jr. is with the Departments of Medicine and Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110 USA (e-mail: [email protected]). This work was supported by the National Science Foundation Grant CCR-0330342 and the Imaging Sciences Pathway program of Washington University in St. Louis. Color versions of one or more of the figures in this paper are available online at http://ieeexplore.ieee.org. Digital Object Identifier 10.1109/TNB.2008.2000745 Fig. 1. (a) RGB image of a oligonucleotide-based microarray. (b) Intensity image of a single spot where the circular outer periphery and the elliptical center hole are shown using dashed lines.
PY - 2008/6
Y1 - 2008/6
N2 - In oligonucleotide microarray experiments, noise is a challenging problem, as biologists now are studying their organisms not in isolation but in the context of a natural environment. In low photomultiplier tube (PMT) voltage images, weak gene signals and their interactions with the background fluorescence noise are most problematic. In addition, nonspecific sequences bind to array spots intermittently causing inaccurate measurements. Conventional techniques cannot precisely separate the foreground and the background signals. In this paper, we propose analytically based estimation technique. We assume a priori spot-shape information using a circular outer periphery with an elliptical center hole. We assume Gaussian statistics for modeling both the foreground and background signals. The mean of the foreground signal quantifies the weak gene signal corresponding to the spot, and the variance gives the measure of the undesired binding that causes fluctuation in the measurement. We propose a foreground-signal and shape-estimation algorithm using the Gibbs sampling method. We compare our developed algorithm with the existing Mann-Whitney (MW)- and expectation maximization (EM)/iterated conditional modes (ICM)-based methods. Our method outperforms the existing methods with considerably smaller mean-square error (MSE) for all signal-to-noise ratios (SNRs) in computer-generated images and gives better qualitative results in low-SNR real-data images. Our method is computationally relatively slow because of its inherent sampling operation and hence only applicable to very noisy-spot images. In a realistic example using our method, we show that the gene-signal fluctuations on the estimated foreground are better observed for the input noisy images with relatively higher undesired bindings.
AB - In oligonucleotide microarray experiments, noise is a challenging problem, as biologists now are studying their organisms not in isolation but in the context of a natural environment. In low photomultiplier tube (PMT) voltage images, weak gene signals and their interactions with the background fluorescence noise are most problematic. In addition, nonspecific sequences bind to array spots intermittently causing inaccurate measurements. Conventional techniques cannot precisely separate the foreground and the background signals. In this paper, we propose analytically based estimation technique. We assume a priori spot-shape information using a circular outer periphery with an elliptical center hole. We assume Gaussian statistics for modeling both the foreground and background signals. The mean of the foreground signal quantifies the weak gene signal corresponding to the spot, and the variance gives the measure of the undesired binding that causes fluctuation in the measurement. We propose a foreground-signal and shape-estimation algorithm using the Gibbs sampling method. We compare our developed algorithm with the existing Mann-Whitney (MW)- and expectation maximization (EM)/iterated conditional modes (ICM)-based methods. Our method outperforms the existing methods with considerably smaller mean-square error (MSE) for all signal-to-noise ratios (SNRs) in computer-generated images and gives better qualitative results in low-SNR real-data images. Our method is computationally relatively slow because of its inherent sampling operation and hence only applicable to very noisy-spot images. In a realistic example using our method, we show that the gene-signal fluctuations on the estimated foreground are better observed for the input noisy images with relatively higher undesired bindings.
KW - Gibbs sampling
KW - Low PMT voltage image
KW - Spot segmentation
KW - cDNA microarray
UR - https://www.scopus.com/pages/publications/45249095811
U2 - 10.1109/TNB.2008.2000745
DO - 10.1109/TNB.2008.2000745
M3 - Article
C2 - 18556262
AN - SCOPUS:45249095811
SN - 1536-1241
VL - 7
SP - 142
EP - 153
JO - IEEE Transactions on Nanobioscience
JF - IEEE Transactions on Nanobioscience
IS - 2
M1 - 7
ER -