Abstract: The snag-resistant fishing lure is designed to minimize the chances of the lure becoming ensnared. The lure has a jig and a blade attached to the blade in a configuration that limits the side-to-side movement of the blade, thereby preventing the jig from rolling to a hook-downward position prone to snagging. A centrally aligned hole is positioned close to the front edge of the blade member. An eyelet extending from the jig body is attached through an aperture in the blade. The blade is limited in its side-to-side movement by contact between the blade edge and either the jig body or the eyelet. The limited side-to-side movement of the blade creates a quick, controlled, oscillating blade action that imparts a natural swimming motion to the lure, emulating prey species movements.

Abstract: The snag-resistant fishing lure is a snag-free fishing lure designed to minimize the chances of the lure becoming ensnared. The lure has a jig and a blade attached to the blade in a configuration that limits the side-to-side movement of the blade, thereby preventing the jig from rolling to a hook-downward position prone to snagging. A centrally aligned hole is positioned close to the front edge of the blade member. An eyelet extending from the jig body is attached through an aperture in the blade. The blade is limited in its side-to-side movement by contact between the blade edge and either the jig body or the eyelet. The limited side-to-side movement of the blade creates a quick, controlled, oscillating blade action that imparts a natural swimming motion to the lure, emulating prey species movements.

Abstract: The snag-resistant fishing lure is a snag-free fishing lure designed to minimize the chances of the lure becoming ensnared. The lure has a jig and a blade attached to the blade in a configuration that limits the side-to-side movement of the blade, thereby preventing the jig from rolling to a hook-downward position prone to snagging. A centrally aligned hole is positioned close to the front edge of the blade member. An eyelet extending from the jig body is attached through an aperture in the blade. The blade is limited in its side-to-side movement by contact between the blade edge and either the jig body or the eyelet. The limited side-to-side movement of the blade creates a quick, controlled, oscillating blade action that imparts a natural swimming motion to the lure, emulating prey species movements.

Abstract: Methods and systems are provided for capturing and saving motor drive information in a non-volatile memory to facilitate troubleshooting and motor fault analysis. The motor drive includes a power conversion system that provides electrical power to an electric motor and a control system providing a control input to the power conversion system, and an information capture system is provided with an information capture component to capture motor drive information and a non-volatile memory component to store the captured information.

Abstract: The present invention relates to a biomechanical monitoring apparatus (1) which includes a mounting means adapted to allow the apparatus to be worn by a user and a motion a detection means (2) adapted to detect the motion of a user when the apparatus is worn. The apparatus also includes an accumulation means (4) adapted to indicate the extent of motion activity completed by a user since a specific time. The invention also relates to a method of using such apparatus where the extent of motion activity completed is compared against at least one movement activity threshold level to potentially activate an alarm indicator when such thresholds are exceeded.

Abstract: Methods and systems are provided for capturing and saving motor drive information in a non-volatile memory to facilitate troubleshooting and motor fault analysis. The motor drive includes a power conversion system that provides electrical power to an electric motor and a control system providing a control input to the power conversion system, and an information capture system is provided with an information capture component to capture motor drive information and a non-volatile memory component to store the captured information.

Abstract: A method for producing a single stranded DNA (ssDNA) molecule of a defined length and sequence is disclosed. This method enables the preparation of, inter alia, probes of greater length than can be chemically synthesized. The method starts with a double stranded molecule, such as genomic, double stranded DNA (dsDNA) from any organism. A fragment of the starting molecule (dsDNA) is amplified by specific primers engineered to introduce cleavage sites on either side of the desired sequence. Cleavage steps on the amplified, engineered fragment are combined with a phosphate removal step, thereby creating a construct that can be digested with an exonuclease without damage to the desired ssDNA. Probes, which hybridize with large gaps between the ends of the probes, are also disclosed.

Abstract: An air flow state determining system that determines a mass air flow into a cylinder of an engine having a cam phaser includes a first module that determines whether an air flow state is one of steady-state and transient based on a cam phaser position. A second module determines the mass air flow using one of a mass air flow sensor signal and a speed density relationship based on whether the mass air flow state is one of steady-state and transient.

Abstract: A method of determining the length of a polynucleotide target is provided. With this method, a target is first hybridized to an array of first probes having different, determined lengths, resulting in the formation of duplexes between the polynucleotide target and the first probes. These duplexes have a single stranded section of target if the target is longer than the first probe it is in a duplex with, and a single stranded section of probe if the target is shorter than the first probe it is in a duplex with. Next, a series of probes is hybridized to the duplexes, breaking apart duplexes in which the target and probe have unequal lengths through the process of branch migration. Thus, the target only remains bound in the duplex if the target and probe are of equal lengths. The length of the polynucleotide target can thereby be determined.

Abstract: The invention is directed to novel methods of multiplexing nucleic acid reactions, including amplification, detection and genotyping. The invention relies on the use of precircle probes that are circularized in the presence of the corresponding target nucleic acids, cleaved, and then amplified.

Abstract: The invention encompasses methods for enriching for and identifying a polymorphism within a nucleic acid sample either by separating a subset of a nucleic acid sample or by selectively replicating a subset of a nucleic acid sample such that the polymorphism is contained within a nucleic acid population with reduced complexity, and then identifying the polymorphism within the enriched nucleic acid sample.

Abstract: An inlet air dynamics (IAD) characterization control system for an internal combustion engine includes a first module that estimates a future firing event manifold absolute pressure (MAP) and a second module that determines a MAP cycle difference based on the future firing event MAP and a previous cycle MAP. A third module characterizes an IAD state based on the MAP cycle difference.

Abstract: The invention encompasses methods for enriching for and identifying a polymorphism within a nucleic acid sample either by separating a subset of a nucleic acid sample or by selectively replicating a subset of a nucleic acid sample such that the polymorphism is contained within a nucleic acid population with reduced complexity, and then identifying the polymorphism within the enriched nucleic acid sample.

Abstract: The invention encompasses methods for enriching for and identifying a polymorphism within a nucleic acid sample either by separating a subset of a nucleic acid sample or by selectively replicating a subset of a nucleic acid sample such that the polymorphism is contained within a nucleic acid population with reduced complexity, and then identifying the polymorphism within the enriched nucleic acid sample.

Abstract: A DNA microarray, preferably in the form of a chip, contains probes which hybridize to generate primers capable of amplifying approximately 89 HPV types. These target the E1 region of the gene. The design of the chip allows for the detection of any known HPV type, based on a unique probe sequence derived from the HPV E1 region. The present assay utilizes a number of primers that can amplify from about one to six different types of HPV. A large number of primers can be used together. After amplification, the amplicons are contacted with specific probes that are unique for each HPV type. The array further employs a control sequence, which normalizes variability due to sample size.

Abstract: The invention is directed to novel methods of multiplexing nucleic acid reactions, including amplification, detection and genotyping. The invention relies on the use of precircle probes that are circularized in the presence of the corresponding target nucleic acids, cleaved, and then amplified.

Abstract: A fuel control system delivers fuel to an engine cylinder and compensates for lost fuel. The fuel control system comprises a fuel dynamics module that determines a fuel dynamics model that is indicative of fuel behavior. The fuel dynamic module determines an inverse of the fuel dynamics model, receives a fuel command, and generates an adjusted fuel command based on the fuel command and the inverse of the fuel dynamics model. A lost fuel compensation module receives the adjusted fuel command and generates a final fuel command based on the adjusted fuel command and a lost fuel factor. A control module controls fuel delivery according to the final fuel command.

Abstract: A method for monitoring a chemical component in an industrial water system comprises irradiating a liquid sample from an industrial water system, containing at least one chemical component to be monitored, with light from an excitation light source. Room temperature phosphorescence emitted from the sample is detected after irradiation. The concentration of the chemical component to be monitored is then calculated from the detected room temperature phosphorescence. The liquid sample includes at least one room temperature phosphorescent material (RTPM) and at least one heavy atom perturber (HAP) dissolved therein. The HAP is present in the sample at a concentration sufficient to induce phosphorescence activity in the RTPM. The liquid sample is irradiated in a manner sufficient to induce the RTPM within the sample to emit room temperature phosphorescence, and the calculated concentration of the chemical component to be monitored is a function of the room temperature phosphorescence intensity or temporal metric.

Abstract: An illumination system includes a plurality of radiation generating sources, such as LED dies. A corresponding plurality of optical waveguides is also provided, with each waveguide having a first and a second end, with each first end being in optical communication with the corresponding LED die. An array of corresponding passive optical elements is interposed between the plurality of LED dies and the corresponding first ends of the plurality of optical waveguides. The illumination system provides for substantially high light coupling efficiency and an incoherent light output that can appear to the human observer as arising from a single point of light. In addition, the light can be output remotely at one or more locations and in one or more directions.

Abstract: The present invention features methods and compositions for the renaturation, hybridization, association, or reassociation of nucleic acids that combines both acceleration of the reaction rate and improved specificity.