TY - GEN
T1 - Biomathematics oriented machine learning system for reconstructing temporal profiles of biological or clinical markers
AU - Tal-Botzer, Ronen
AU - Hadaya, Nir
AU - Levy-Drummer, Rachel S.
AU - Feiglin, Ariel
AU - Shalom, David H.
AU - Neumann, Avidan U.
PY - 2006
Y1 - 2006
N2 - Time series reconstruction algorithms are widely used to create temporal profiles from data series. However, in many clinical fields, e.g., viral kinetics, the data is noisy and sparse, making it difficult to use standard algorithms. We developed PROFILASE, which combines advanced multi-objective genetic algorithm search with machine learning architecture to harvest experts' decision-making considerations. Furthermore, PROFILASE implements additional scoring considerations, more biological in nature, thus further exploits domain expertise. We tested our system against a standard bottom-up algorithm by reconstruction of time series sparsely sampled with noise from simulated profiles. PROFILASE obtained RMS distance 2.5 fold lower (P<0.0001) than the standard algorithm, 93% correct identification rate of segment number and 88% correct profile classification rate (versus 68%). The additional considerations were found to have a significant effect on the success of reconstruction. Finally, PROFILASE was generalized to evaluate additional considerations from different fields, thus allowing better understanding of other diseases.
AB - Time series reconstruction algorithms are widely used to create temporal profiles from data series. However, in many clinical fields, e.g., viral kinetics, the data is noisy and sparse, making it difficult to use standard algorithms. We developed PROFILASE, which combines advanced multi-objective genetic algorithm search with machine learning architecture to harvest experts' decision-making considerations. Furthermore, PROFILASE implements additional scoring considerations, more biological in nature, thus further exploits domain expertise. We tested our system against a standard bottom-up algorithm by reconstruction of time series sparsely sampled with noise from simulated profiles. PROFILASE obtained RMS distance 2.5 fold lower (P<0.0001) than the standard algorithm, 93% correct identification rate of segment number and 88% correct profile classification rate (versus 68%). The additional considerations were found to have a significant effect on the success of reconstruction. Finally, PROFILASE was generalized to evaluate additional considerations from different fields, thus allowing better understanding of other diseases.
UR - https://www.scopus.com/pages/publications/33845584508
U2 - 10.1109/cbms.2006.61
DO - 10.1109/cbms.2006.61
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AN - SCOPUS:33845584508
SN - 0769525172
SN - 9780769525174
T3 - Proceedings - IEEE Symposium on Computer-Based Medical Systems
SP - 563
EP - 568
BT - Proceedings - 19th IEEE International Symposium on Computer-Based Medical Systems, CBMS 2006
T2 - 19th IEEE International Symposium on Computer-Based Medical Systems, CBMS 2006
Y2 - 22 June 2006 through 23 June 2006
ER -