A system comprising a plurality of neuromuscular sensors, each of which is configured to record a time-series of neuromuscular signals from a surface of a user's body; and at least one computer hardware processor programmed to perform: applying a source separation technique to the time series of neuromuscular signals recorded by the plurality of neuromuscular sensors to obtain a plurality of neuromuscular source signals and corresponding mixing information; providing features, obtained from the plurality of neuromuscular source signals and/or the corresponding mixing information, as input to a trained statistical classifier and obtaining corresponding output; and identifying, based on the output of the trained statistical classifier, and for each of one or more of the plurality of neuromuscular source signals, an associated set of one or more biological structures.

A diagnosis report generation method and terminal device are provided. The method includes obtaining electrocardiography ECG data, determining that the ECG data includes abnormal heartbeat data, obtaining, based on the ECG data, an abnormal heartbeat waveform corresponding to the abnormal heartbeat data, combining a normal heartbeat waveform and the abnormal heartbeat waveform to obtain an abnormality comparison image, and generating a diagnosis report based on the abnormality comparison image. The abnormal heartbeat waveform is obtained by extracting and analyzing the ECG data, so that the abnormal heartbeat waveform can be combined and compared with the normal heartbeat waveform, to obtain the abnormality comparison image for generating the diagnosis report.

According to one embodiment, a data processing device includes an acquisition part, and a processor. The acquisition part is configured to acquire first data including time-series image data. The processor is configured to derive first feature information based on a multidimensional array of n dimensions based on the first data acquired by the acquisition part. n is an integer not less than 3. A first axis of the multidimensional array is related to time.

A system comprising a plurality of neuromuscular sensors, each of which is configured to record a time-series of neuromuscular signals from a surface of a user's body; and at least one computer hardware processor programmed to perform: applying a source separation technique to the time series of neuromuscular signals recorded by the plurality of neuromuscular sensors to obtain a plurality of neuromuscular source signals and corresponding mixing information; providing features, obtained from the plurality of neuromuscular source signals and/or the corresponding mixing information, as input to a trained statistical classifier and obtaining corresponding output; and identifying, based on the output of the trained statistical classifier, and for each of one or more of the plurality of neuromuscular source signals, an associated set of one or more biological structures.

Detecting a counterfeit status of a target device by: selecting a set of frequencies that best reflect load dynamics or other information content of a reference device while undergoing a power test sequence; obtaining target electromagnetic interference (EMI) signals emitted by the target device while undergoing the same power test sequence; creating a sequence of target kiviat plots from the amplitude of the target EMI signals at each of the set of frequencies at observations over the power test sequence to form a target kiviat tube EMI fingerprint; comparing the target kiviat tube EMI fingerprint to a reference kiviat tube EMI fingerprint for the reference device undergoing the power test sequence to determine whether the target device and the reference device are of the same type; and generating a signal to indicate a counterfeit status based at least in part on the results of the comparison.

Similarities between events that include a plurality of dimensions are computed, the similarities computed based on binary comparisons between the events and based on user-specified weights for the dimensions. Multidimensional scaling (MDS) values are calculated based on the computed similarities between the events. A graphical visualization is generated of a temporal plot of the events, the temporal plot comprising a first axis corresponding to time, and a second axis corresponding to the MDS values, and the temporal plot representing overlapping time slices each containing pixels representing a respective subset of the events.

An information processing terminal capable of communicating with a sensor terminal including a first biological sensor which measures a first type of biological information includes: a reception unit receiving a measurement result of the first biological sensor from the sensor terminal; a second biological sensor measuring the first type of biological information; and a control unit authenticating the sensor terminal and establishing connection with the sensor terminal when the measurement result of the first biological sensor satisfies a predetermined condition on a measurement result of the second biological sensor.

A method and system for determining a patient's risk of ventricular tachycardia are disclosed. The method includes receiving ECG signals from a patient and filtering the collected ECG signals to generate filtered ECG signals. The method further includes identifying a heart vector from the filtered ECG signals, and measuring a velocity of the heart vector movement. A change in curvature of the identified heart vector movement is quantified and a risk of ventricular tachycardia is determined based at least on the measured velocity and the quantified change in curvature of the identified heart vector movement.

A data processing method for detecting the conversion from mild cognitive impairment (MCI) to Alzheimer disease (AD), allowing objectively quantifying the effects that this has on the patient's electroencephalogram (EEG). The method of the invention provides an objective criterion for monitoring the brain health status of MCI subjects, which goes alongside the other criteria of neurological, psychological, clinical and cognitive assessment normally provided by the evaluation protocols of these patients.

Detecting a counterfeit status of a target utility device by: selecting a set of frequencies that best reflect load dynamics or other information content of a reference utility device while undergoing a power test sequence; obtaining target electromagnetic interference (EMI) signals emitted by the target utility device while undergoing the same power test sequence; creating a sequence of target kiviat plots from the amplitude of the target EMI signals at each of the set of frequencies at observations over the power test sequence to form a target kiviat tube EMI fingerprint; comparing the target kiviat tube EMI fingerprint to a reference kiviat tube EMI fingerprint for the reference utility device undergoing the power test sequence to determine whether the target utility device and the reference utility device are of the same type; and generating a signal to indicate a counterfeit status based at least in part on the results of the comparison.