Abstract: Systems and methods (e.g., utilities) for use in providing automated data quality detection that can be used multiple times across various domains and across multiple data quality spheres. A data structure or schema of an incoming data set is initially mapped to a desired data or knowledge state in a domain ontology made up of a number of TBox statements. Data quality issues in the incoming data set can then be detected as instances of the incoming data set are attempted to be inferenced against or otherwise matched to anticipated TBox statements of the domain ontology.

Abstract: A biosensor includes a microfluidics layer, a transduction layer and a transceiver layer. The transduction layer further includes a functionalized layer that reacts with a biomarker, and a plurality of carbon nanotubes adjacent the functionalized layer. The conductivity of the carbon nanotubes changes in response to a biomarker reacting with at least a portion of the functionalized layer. The functionalized layer can include dendrimers, such as a tadpole dendrimer scaffolding that includes a plurality of sites for receiving receptors for biomarkers.

Abstract: Aspects of the disclosure include a threat detecting apparatus. The threat detecting apparatus can include an interface circuit, an opcode detector, and a pattern analyzer. The interface circuit is configured to receive a data stream. The opcode detector can be configured to identify an opcode sequence embedded in the data stream based on a first model graph that includes a plurality of interconnected token nodes. Each token node is representative of an occurrence or a non-occurrence of a token. The pattern analyzer may be configured to identify an opcode signature embedded in the identified opcode sequence based on a second model graph, and to output a signal indicative of the successful identification of the opcode signature. The second model graph can include a plurality of interconnected opcode nodes, and each opcode node can be representative of an occurrence or a non-occurrence of a predetermined combination of one or more opcodes.

Abstract: Aspects of the disclosure include a threat detecting apparatus. The threat detecting apparatus can include an interface circuit, an opcode detector, and a pattern analyzer. The interface circuit is configured to receive a data stream. The opcode detector can be configured to identify an opcode sequence embedded in the data stream based on a first model graph that includes a plurality of interconnected token nodes. Each token node is representative of an occurrence or a non-occurrence of a token. The pattern analyzer may be configured to identify an opcode signature embedded in the identified opcode sequence based on a second model graph, and to output a signal indicative of the successful identification of the opcode signature. The second model graph can include a plurality of interconnected opcode nodes, and each opcode node can be representative of an occurrence or a non-occurrence of a predetermined combination of one or more opcodes.

Abstract: Aspects of the disclosure provide a system for signal processing. The system includes a selection circuitry and a coordination detection circuitry. The selection circuitry is configured to receive data sets sampled at different time for a subject and select a plurality of data units from each data set that corresponds to regions of interests in the data set. The coordination detection circuitry is configured to receive the selected data units corresponding to the regions of interests over time, and detect a coordination of the regions of interests over time.

Abstract: A microfluidic cartridge can include at least one nucleic acid analysis portion. Each nucleic acid analysis portion can include a fluidic network being configured for micro-liter volumes or less, a sample input at the beginning of the fluidic network, a plurality of vent ports and fluidic channels in the fluidic network configured to effectuate hydrodynamic movement within the fluidic network, an extraction mixture reservoir in the fluidic network, a mixing chamber in the fluidic network, an amplification chamber in the fluidic network, and a separation channel in the fluidic network. A nucleic acid analyzer can be capable of performing nucleic acid analysis using the microfluidic cartridge. A nucleic acid analysis method can be performed using the microfluidic cartridge.

Abstract: Aspects of the disclosure provide an iris recognition system. The iris recognition system can include a three-dimensional (3D) sensor that is configured to capture a 3D image of an iris, an iris feature extractor that is configured to generate an iris template based on the 3D image of the iris, and a memory that is configured to store the iris template.

Abstract: A system is disclosed including a cylindrical device, having at least one transparent path therethrough, configured to support a thermal dye printer film, the film comprising at least one color panel, a light source configured to illuminate through the cylindrical device at an absorption wavelength of the at least one color panel of the film, and an imaging device configured to capture an image of the film with light emitted at the absorption wavelength of the at least one color panel of the film at a target location on the cylindrical device. Another system and a method are also disclosed.

Abstract: This document relates to systems and method for latent fingerprint detection using specular reflection (glare). An exemplary system may include a light source alignment portion configured to align a light source at an illumination angle relative to a sample surface such that the light source illuminates a sample surface so that the surface produces specular reflection. The system may also include a specular reflection discriminator that directs the produced specular reflection to an optical detector aligned relative to said sample surface at an alignment angle that is substantially equal to an angle of reflection of the produced specular reflection. Preferably, the directed specular reflection does not saturate the optical detector; and the optical detector captures the specular reflection from the sample surface and generates image data using essentially only the specular reflection.

Abstract: Systems and methods for image processing are disclosed. For example, a system for processing images includes voxel-ranking circuitry that ranks individual voxels using voxel data derived from physiological responses resulting from exposure to a plurality of corresponding baseline stimulus images, and voxel selection circuitry that selects a portion of the set of ranked voxels based on their rank.

Abstract: Aspects of the disclosure provide a microfluidic chip to facilitate DNA analysis. The microfluidic chip includes a first domain configured for polymerase chain reaction (PCR) amplification of DNA fragments, a dilution domain coupled to the first domain to dilute a PCR mixture received from the first domain, and a second domain that is coupled to the dilution domain so as to receive the amplified DNA fragments. The second domain includes a separation channel that is configured to perform electrophoretic separation of the amplified DNA fragments. In addition, the disclosure provides a DNA analyzer to act on the microfluidic chip to perform an integrated single chip DNA analysis.

Abstract: Aspects of the disclosure provide a microfluidic chip. The microfluidic chip includes a first domain configured for polymerase chain reaction (PCR) amplification of DNA fragments, and a second domain for electrophoretic separation. The first domain includes at least a first reaction reservoir designated for PCR amplification based on a first sample, and a second reaction reservoir designated for PCR amplification based on a second sample. The second domain includes at least a first separation unit coupled to the first reaction reservoir to received first amplified DNA fragments based on the first sample, and a second separation unit coupled to the second reaction reservoir to received second amplified DNA fragments based on the second sample. The first separation unit is configured to perform electrophoretic separation for the first amplified DNA fragments, and the second separation unit is configured to perform electrophoretic separation for the second amplified DNA fragments.