A data transmission system for transmitting an electrical data to a nerve cell. A data receiving system for receiving an electrical data from a nerve cell has at least two phototransistor crystals that is stimulated by light to form an electrical signal; an image source that allows the light to be sent to the phototransistor crystals and allows controlling the amount of light transmitted to each phototransistor crystal independently of each other, and at least one control unit that is connected to the image source that controls the amount of light transmitted from the image source to each of the phototransistor crystals.

A data transmission system for transmitting an electrical data to a nerve cell. A data receiving system for receiving an electrical data from a nerve cell has at least two phototransistor crystals that is stimulated by light to form an electrical signal; an image source that allows the light to be sent to the phototransistor crystals and allows controlling the amount of light transmitted to each phototransistor crystal independently of each other, and at least one control unit that is connected to the image source that controls the amount of light transmitted from the image source to each of the phototransistor crystals.

A device includes a sensor signal input node and a high-pass filter stage. The high-pass filter stage includes an operational amplifier and a feedback integrator. The operational amplifier includes an input node coupled to the sensor signal input node. The feedback integrator is coupled between an output node of the operational amplifier and the input node of the operational amplifier to set a high-pass pole frequency of the high-pass filter stage.

A method enables analysis of (e.g. bioelectric) signals acquired by measurement. The method provides N signals U for an observation space and each has a time- and space-dependent signal characteristic U. Digitized signals for a time period T have M time points and define an M×N matrix with M tuples of N signal values each. Signal values acquired at time t form an N-tuple Ū.sub.t=(U.sub.1, . . . , U.sub.N).sub.t in a signal space. The method acquires all combinations of k tuples from the M tuples, and calculates distances between all tuples. Distance values are calculated and define edge lengths of a (k−1) simplex (SIM) with one simplex assigned to each combination of k time points. Quantity characteristics of the simplex (SIM) are encoded into color values (COL), and displays the colors in a combinatorial time lattice (CTL). Each lattice point (GP) is displayed with the color encoded for the assigned simplex.

A method enables analysis of (e.g. bioelectric) signals acquired by measurement. The method provides N signals U for an observation space and each has a time- and space-dependent signal characteristic U. Digitized signals for a time period T have M time points and define an M×N matrix with M tuples of N signal values each. Signal values acquired at time t form an N-tuple Ū.sub.t=(U.sub.1, . . . , U.sub.N).sub.t in a signal space. The method acquires all combinations of k tuples from the M tuples, and calculates distances between all tuples. Distance values are calculated and define edge lengths of a (k−1) simplex (SIM) with one simplex assigned to each combination of k time points. Quantity characteristics of the simplex (SIM) are encoded into color values (COL), and displays the colors in a combinatorial time lattice (CTL). Each lattice point (GP) is displayed with the color encoded for the assigned simplex.

Provided herein are systems and methods for calculating patient information. The method includes determining a transfer matrix, recording electric potentials via a first set of recording electrodes located at a first set of recording locations to create a first set of recorded signals, and calculating patient information for a set of target locations by applying the transfer matrix to the first set of recorded signals. The transfer matrix is a characterization of electrical properties of tissue between the first set of recording locations and the set of target locations.

A pulse transit time measurement device according to an aspect includes: a belt unit; a plurality of first electrodes and second electrodes provided on the belt unit; a third electrode provided on the belt unit; a first electrocardiographic signal acquisition unit that acquires a first electrocardiographic signal of a user using the plurality of first electrodes; a second electrocardiographic signal acquisition unit that acquires a second electrocardiographic signal of the user with the second electrode and the third electrode; a feature amount parameter calculation unit that calculates a feature amount parameter related to a waveform feature point of the first electrocardiographic signal on the basis of a waveform feature point of the second electrocardiographic signal; a pulse wave signal acquisition unit that acquires a pulse wave signal representing a pulse wave of the user; and a pulse transit time calculation unit that detects a waveform feature point.

The present application discloses a PPG circuit, a biological characteristics detection device and a biological characteristics detection method. The PPG circuit is configured to control a light source and N photoelectric converters to sense biological characteristics of an object under test; the PPG circuit includes: a transmitting channel, K receiving channels, wherein the N photoelectric converters are divided into K sets of photoelectric converter sets, and the K receiving channels respectively correspond to K sets of photoelectric converter sets; and a controller, configured to control the PPG circuit to operate in a partial sampling phase or an full sampling phase, so as to generates J or K biological characteristics sampling results during each of the pulse repetition cycles.

The present application discloses a PPG circuit, a biological characteristics detection device and a biological characteristics detection method. The PPG circuit is configured to control a light source and N photoelectric converters to sense biological characteristics of an object under test; the PPG circuit includes: a transmitting channel, K receiving channels, wherein the N photoelectric converters are divided into K sets of photoelectric converter sets, and the K receiving channels respectively correspond to K sets of photoelectric converter sets; and a controller, configured to control the PPG circuit to operate in a partial sampling phase or an full sampling phase, so as to generates J or K biological characteristics sampling results during each of the pulse repetition cycles.

Example devices are disclosed herein that include a first elongated band coupled to a first housing to be located on a first side of a head of a subject and a second housing to be located near a second side of the head of the subject, the first elongated band comprising a first set of electrodes. The example device also includes a second elongated band coupled to the first housing and to the second housing, the second elongated band comprising a second set of electrodes. In addition, the device includes a third elongated band coupled to the first housing and to the second housing, the third elongated band comprising a third set of electrodes.