TY - GEN
T1 - Forward error correcting biosensors
T2 - 2008 IEEE-BIOCAS Biomedical Circuits and Systems Conference, BIOCAS 2008
AU - Liu, Yang
AU - Alocilja, Evangelyn
AU - Chakrabartty, Shantanu
PY - 2008
Y1 - 2008
N2 - Advances in micro-nano-biosensor fabrication are enabling the integration of a large number of biological recognition elements within a single package. As a result, hundreds to millions of tests can be performed simultaneously and can facilitate rapid detection of multiple pathogens in a given sample. However, it is an open question as to how to exploit the highdimensional nature of the multi-pathogen testing for improving the detection reliability of typical biosensor systems. Our research over the past few years has addressed this question and in this paper we briefly summarize our approach. Our underlying principle is based on a forward error correcting (FEC) biosensor where redundant patterns are synthetically encoded on the biosensor. A decoding algorithm then exploits this redundancy to compensate for systematic errors due to experimental variations and for random errors due to stochastic biomolecular interactions. The key milestones in this research are : (a) fabrication and modeling of biomolecular circuit elements used for constructing the FEC biosensor; (b) development of a simulation environment for rapid evaluation of encoding/decoding algorithms and (c) development of a "co-detection" protocol that exploits non-linear interaction between different biomolecular circuit elements. As a proof-of-concept our study and experimental results have been based on a conductimetric lateral flow immunosensor that uses antigen-antibody interaction in conjunction with a polyaniline transducer to detect the presence or absence of pathogens in a given sample.
AB - Advances in micro-nano-biosensor fabrication are enabling the integration of a large number of biological recognition elements within a single package. As a result, hundreds to millions of tests can be performed simultaneously and can facilitate rapid detection of multiple pathogens in a given sample. However, it is an open question as to how to exploit the highdimensional nature of the multi-pathogen testing for improving the detection reliability of typical biosensor systems. Our research over the past few years has addressed this question and in this paper we briefly summarize our approach. Our underlying principle is based on a forward error correcting (FEC) biosensor where redundant patterns are synthetically encoded on the biosensor. A decoding algorithm then exploits this redundancy to compensate for systematic errors due to experimental variations and for random errors due to stochastic biomolecular interactions. The key milestones in this research are : (a) fabrication and modeling of biomolecular circuit elements used for constructing the FEC biosensor; (b) development of a simulation environment for rapid evaluation of encoding/decoding algorithms and (c) development of a "co-detection" protocol that exploits non-linear interaction between different biomolecular circuit elements. As a proof-of-concept our study and experimental results have been based on a conductimetric lateral flow immunosensor that uses antigen-antibody interaction in conjunction with a polyaniline transducer to detect the presence or absence of pathogens in a given sample.
KW - Co-detection
KW - Factor graph
KW - Forward error correcting biosensors
KW - Sum-product algorithm
UR - https://www.scopus.com/pages/publications/63649125676
U2 - 10.1109/BIOCAS.2008.4696921
DO - 10.1109/BIOCAS.2008.4696921
M3 - Conference contribution
AN - SCOPUS:63649125676
SN - 9781424428793
T3 - 2008 IEEE-BIOCAS Biomedical Circuits and Systems Conference, BIOCAS 2008
SP - 249
EP - 252
BT - 2008 IEEE-BIOCAS Biomedical Circuits and Systems Conference, BIOCAS 2008
Y2 - 20 November 2008 through 22 November 2008
ER -