Abstract: Automated generation of schema and interface methods is described. The system receives a schema definition file, which in one aspect of the system is an XML file. The system parses the schema definition file into an internal representation comprising collection classes. A SQL generator traverses the collection classes and generates SQL statements that define tables, views and stored procedures. A component generator traverses the collection classes and generates computer program source code implementing components that access properties defined in the schema definition data, and methods that provide for persistent storage of the objects in a database.

Abstract: A fireplace fire starting device for efficiently starting campfires and fireplace fires. The fireplace fire starting device includes a housing. The housing comprises a shaft, which is elongate and has a first end and a second end. A peripheral wall extends between and is integrally coupled to the first and second ends. The shaft has a lumen therein. The peripheral wall has a plurality of openings therein. Each of the openings extends into the lumen, and each of the openings is generally aligned. Burning oil is placed in the lumen. The shaft is placed in a fireplace under the wood grill, and the burning oil in the lumen is lit such that flames escape upwards and ignite wood on the wood supporting grill.

Abstract: The present invention provides methods and apparatus for detecting and discriminating multiple analytes within a test sample which are rapid, accurate, and convenient enough for routine use in a clinical laboratory. In particular, the present invention provides methods and apparatus for permitting multiple PCR-amplified target nucleic acid sequence hybrids within a single sample, labeled with different fluorescent dyes, to be spectrally distinguished using the read-out data directly from a fluorescence reader instrument.

Abstract: The present invention provides methods and apparatus for detecting and discriminating multiple analytes within a test sample which are simple, user-friendly, cost-effective and fast. In particular, it is preferred that the overall time for sample preparation, nucleic acid sequence amplification, and nucleic acid sequence differentiation be about 5 hours or less.

Abstract: The present invention provides methods and apparatus for detecting and discriminating multiple analytes within a test sample which are simple, user-friendly, cost-effective and fast. In particular, it is preferred that the overall time for sample preparation, nucleic acid sequence amplification, and nucleic acid sequence differentiation be about 5 hours or less.

Abstract: The present invention provides methods and apparatus for detecting and discriminating multiple analytes within a test sample which are simple, user-friendly, cost-effective and fast. In particular, it is preferred that the overall time for sample preparation, nucleic acid sequence amplification, and nucleic acid sequence differentiation be about 5 hours or less.

Abstract: The present invention provides methods and apparatus for detecting and discriminating multiple analytes within a test sample which are simple, user-friendly, cost-effective and fast. In particular, it is preferred that the overall time for sample preparation, nucleic acid sequence amplification, and nucleic acid sequence differentiation be about 5 hours or less.

Abstract: The present invention provides methods and apparatus for detecting and discriminating multiple analytes within a test sample which are rapid, accurate, and convenient enough for routine use in a clinical laboratory. In particular, the present invention provides methods and apparatus for permitting multiple PCR-amplified target nucleic acid sequence hybrids within a single sample, labeled with different fluorescent dyes, to be spectrally distinguished using the read-out data directly from a fluorescence reader instrument.

Abstract: The present invention provides methods and apparatus for detecting and discriminating multiple analytes within a test sample which are simple, user-friendly, cost-effective and fast. In particular, it is preferred that the overall time for sample preparation, nucleic acid sequence amplification, and nucleic acid sequence differentiation be about 5 hours or less.