Quantitative estimation of the workload in the brain is an important factor for helping to predict the behavior of humans. The reaction time when performing a difficult task is longer than that when performing an easy task. Thus, the reaction time reflects the workload in the brain. In this study, we employed an N-back task in order to regulate the degree of difficulty of the tasks, and then estimated the reaction times from the brain activity. The brain activity that we used to estimate the reaction time was the auditory steady-state response (ASSR) evoked by a 40-Hz click sound. Fifteen healthy participants participated in the present study and magnetoencephalogram (MEG) responses were recorded using a 148-channel magnetometer system. The least absolute shrinkage and selection operator (LASSO), which is a type of sparse modeling, was employed to estimate the reaction times from the ASSR recorded by MEG. The LASSO showed higher estimation accuracy than the least squares method. This result indicates that LASSO overcame the over-fitting to the learning data. Furthermore, the LASSO selected channels in not only the parietal region, but also in the frontal and occipital regions. Since the ASSR is evoked by auditory stimuli, it is usually large in the parietal region. However, since LASSO also selected channels in regions outside the parietal region, this suggests that workload-related neural activity occurs in many brain regions. In the real world, it is more practical to use a wearable electroencephalography device with a limited number of channels than to use MEG. Therefore, determining which brain areas should be measured is essential. The channels selected by the sparse modeling method are informative for determining which brain areas to measure.
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http://dx.doi.org/10.1109/EMBC.2015.7319921 | DOI Listing |
Pol J Vet Sci
December 2024
Anhui Province Key Laboratory of Veterinary Pathobiology and Disease Control, College of Animal Science and Technology, Anhui Agricultural University, Hefei, Anhui 230036, PR China. Email:
The aim of this study was to develop a rapid, sensitive and highly specific TaqMan quantitative real-time polymerase chain reaction PCR (qPCR) assay for porcine circovirus-like virus (PCLV). The primers and probe were designed based on the conserved regions of the PCLV ORF4 gene. The assay has a good detection performance (y=-3.
View Article and Find Full Text PDFPol J Vet Sci
December 2024
School of Biotechnology and Food Engineering, Anyang Institute of Technology, Anyang, China.
Pseudorabies virus (PRV) is one of the most important infectious diseases which leads to significant economic losses in the global swine industry. The gE-deleted vaccine is widely used to prevent susceptible pigs from PRV infection. There is no report of the differentiation of PRV wild strain and vaccine strain by recombinase polymerase amplification (RPA) coupled with a lateral flow dipstick (LFD) method.
View Article and Find Full Text PDFNano Lett
December 2024
Department of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.
Single-walled carbon nanotubes (SWCNTs) are fluorescent materials that have been developed as sensors for measuring the activities of enzymes. However, most sensors to date rely on end-point measurement and empirical functions to correlate enzyme concentrations with fluorescence responses. Less emphasis is put on analyzing time-dependent fluorescence responses and their connections with enzymatic kinetics.
View Article and Find Full Text PDFFront Biosci (Schol Ed)
December 2024
Laboratory of Intracellular Membranes Dynamics, Institute of Cytology of the Russian Academy of Sciences, 194064 Saint Petersburg, Russia.
Background: Real-time reverse transcription quantitative polymerase chain reaction (RT-qPCR) is a powerful tool for analysing target gene expression in biological samples. To achieve reliable results by RT-qPCR, the most stable reference genes must be selected for proper data normalisation, particularly when comparing cells of different types. We aimed to choose the least variable candidate reference genes among eight housekeeping genes tested within a set of human cancer cell lines (HeLa, MCF-7, SK-UT-1B, A549, A431, SK-BR-3), as well as four lines of normal, non-malignant mesenchymal stromal cells (MSCs) of different origins.
View Article and Find Full Text PDFFront Biosci (Elite Ed)
October 2024
Department of Medical Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, 1983969411 Tehran, Iran.
Background: Regenerative endodontics requires an innovative delivery system to release antibiotics/growth factors in a sequential trend. This study focuses on developing/characterizing a thermoresponsive core-shell hydrogel designed for targeted drug delivery in endodontics.
Methods: The core-shell chitosan-alginate microparticles were prepared by electrospraying to deliver bone morphogenic protein-2 for 14 days and transforming growth factor-beta 1 (TGF-β1) for 7-14 days.
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