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Development of Altera NIOS II soft-core system to predict total Hemoglobin using multivariate analysis

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dc.contributor.author Pinto, C.F.
dc.contributor.author Parab, J.S.
dc.contributor.author Sequeira, M.
dc.contributor.author Naik, G.M.
dc.date.accessioned 2021-07-05T04:46:14Z
dc.date.available 2021-07-05T04:46:14Z
dc.date.issued 2021
dc.identifier.citation Journal of Physics: Conference Series. 1921; 2021; ArticleID_012039. en_US
dc.identifier.uri https://doi.org/10.1088/1742-6596/1921/1/012039
dc.identifier.uri http://irgu.unigoa.ac.in/drs/handle/unigoa/6487
dc.description.abstract In Today's world, Hemoglobin is measured using an invasive method. This method leads to delayed diagnosis, painful experiences for patients, and a lot of biomedical waste. To overcome these problems, an Altera NIOS II soft-core based system was built to monitor hemoglobin non-invasively. The heart of the system is NIOS II soft-core processor which was configured on the DE0 Nano FPGA board having Cyclone IV EP4CE22F17C6N. This system also has a finger probe which consists of five LED sources (670 nm, 770 nm, 810nm, 850nm and 950nm) and a photodetector (OPT101) to acquire the signal using photoplethysmography (PPG). The incoming real-time PPG signal is recorded at five different wavelengths for fifteen individual subjects. Before applying Multivariate Partial Least Square Regression (PLSR), mathematical empirical formulas was used to predict hemoglobin which gave Root Mean Square Error (RMSE) of 0.442 g/dL and the prediction accuracy of 97.05 percent. To further improve the system accuracy, the PLSR model was implemented on the NIOS II soft-core system. With this, the hemoglobin was predicted with an accuracy of 98.98 percent and a RMSE of 0.179 g/dL. The designed system was validated with Bland-Altman analysis which shows good agreement between predicted and reference hemoglobin en_US
dc.publisher IOP Publishing en_US
dc.subject Electronics en_US
dc.title Development of Altera NIOS II soft-core system to predict total Hemoglobin using multivariate analysis en_US
dc.type Conference article en_US
dc.identifier.impf cs


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