TY - JOUR
T1 - Statistical design of position-encoded microsphere arrays
AU - Sarder, Pinaki
AU - Nehorai, Arye
N1 - Funding Information:
Manuscript received February 19, 2010; revised September 11, 2010; accepted December 19, 2010. Date of publication February 22, 2011; date of current version April 27, 2011. This work was supported by the Department of Defense under the Air Force Office of Scientific Research MURI Grant FA9550-05-1-0443, and NSF Grants CCF-1014908 and CCF-0963742. Asterisk indicates corresponding author. *P. Sarder is with the Department of Biostatistics, Harvard School of Public Health, Boston, MA 02115, USA (e-mail: [email protected]).
PY - 2011/3
Y1 - 2011/3
N2 - We propose a microsphere array device with microspheres having controllable positions for error-free target identification. We conduct a statistical design analysis to select the optimal distance between the microspheres as well as the optimal temperature. Our design simplifies the imaging and ensures a desired statistical performance for a given sensor cost. Specifically, we compute the posterior Cramér-Rao bound on the errors in estimating the unknown target concentrations. We use this performance bound to compute the optimal design variables. We discuss both uniform and sparse concentration levels of targets, and replace the unknown imaging parameters with their maximum likelihood estimates. We illustrate our design concept using numerical examples. The proposed microarray has high sensitivity, efficient packing, and guaranteed imaging performance. It simplifies the imaging analysis significantly by identifying targets based on the known positions of the microspheres. Potential applications include molecular recognition, specificity of targeting molecules, proteinprotein dimerization, high throughput screening assays for enzyme inhibitors, drug discovery, and gene sequencing.
AB - We propose a microsphere array device with microspheres having controllable positions for error-free target identification. We conduct a statistical design analysis to select the optimal distance between the microspheres as well as the optimal temperature. Our design simplifies the imaging and ensures a desired statistical performance for a given sensor cost. Specifically, we compute the posterior Cramér-Rao bound on the errors in estimating the unknown target concentrations. We use this performance bound to compute the optimal design variables. We discuss both uniform and sparse concentration levels of targets, and replace the unknown imaging parameters with their maximum likelihood estimates. We illustrate our design concept using numerical examples. The proposed microarray has high sensitivity, efficient packing, and guaranteed imaging performance. It simplifies the imaging analysis significantly by identifying targets based on the known positions of the microspheres. Potential applications include molecular recognition, specificity of targeting molecules, proteinprotein dimerization, high throughput screening assays for enzyme inhibitors, drug discovery, and gene sequencing.
KW - Maximum likelihood estimation
KW - microsphere array
KW - optimal statistical design
KW - position-encoding
KW - posterior Cramér-Rao bound
UR - https://www.scopus.com/pages/publications/79955632274
U2 - 10.1109/TNB.2010.2103570
DO - 10.1109/TNB.2010.2103570
M3 - Article
C2 - 21342857
AN - SCOPUS:79955632274
SN - 1536-1241
VL - 10
SP - 16
EP - 29
JO - IEEE Transactions on Nanobioscience
JF - IEEE Transactions on Nanobioscience
IS - 1
M1 - 5716677
ER -