Abstract: This disclosure describes a mounting platform comprising a retainer plate opening that includes a first opening profile at a top platform surface of the mounting platform and a second opening profile at a bottom platform surface of the mounting platform. the top platform surface first receives a retainer plate when nested within the mounting platform, and the bottom platform surface abuts the retainer plate when the retainer plate is nested within the mounting platform. The first opening profile matches a planform profile of the retainer plate and is etched into the top platform surface through to the bottom platform surface, and the second opening profile is etched from midway between the top platform surface and the bottom platform surface through to the bottom platform surface. The second opening profile corresponding to a rotational offset of the first opening profile by a predetermined angle.

Abstract: Compositions and methods for making a plurality of probes for analyzing a plurality of nucleic acid samples are provided. Compositions and methods for analyzing a plurality of nucleic acid samples to obtain sequence information in each nucleic acid sample are also provided.

Abstract: Compositions and methods for making a plurality of probes for analyzing a plurality of nucleic acid samples are provided. Compositions and methods for analyzing a plurality of nucleic acid samples to obtain sequence information in each nucleic acid sample are also provided.

Abstract: Compositions and methods for making a plurality of probes for analyzing a plurality of nucleic acid samples are provided. Compositions and methods for analyzing a plurality of nucleic acid samples to obtain sequence information in each nucleic acid sample are also provided.

Abstract: Compositions and methods for making a plurality of probes for analyzing a plurality of nucleic acid samples are provided. Compositions and methods for analyzing a plurality of nucleic acid samples to obtain sequence information in each nucleic acid sample are also provided.

Abstract: A switch-scanning circuit includes a chip and switching units. The chip includes pins having an output operation mode and an input operation mode, and a processing unit. The processing unit sets one of the pins as an input pin and the rest of the pins as output pins sequentially according to a clock signal, uses a scan signal to provide different voltages to the output pins, and then determines states of button switches according to a voltage of the input pin. The switching unit includes a power source resistance, switches and resistors. A first terminal and a second terminal of the power source resistance are electrically connected to a power source and a first pin respectively. The resistors have terminals electrically connected the first pin and terminals of the switches. The other terminals of the switches are connected to the pins other than the first pin.

Abstract: In one embodiment, a method comprising receiving a logical signal; driving a source voltage at a first circuit node using a driver circuit; generating an impulsive edge signal by detecting a transition of the logical signal; converting the impulsive edge signal into an impulsive charge pump current using a charge pump circuit; injecting the impulsive charge pump current into the first circuit node; transmitting the source voltage to a second circuit node via a transmission line; and terminating the second circuit node with a load.

Abstract: In one embodiment, a method comprising receiving a logical signal; driving a source voltage at a first circuit node using a driver circuit in accordance with the logical signal; controlling an output impedance of the driver circuit using a finite state machine (FSM); transmitting the source voltage to a second circuit node via a transmission line; and terminating the second circuit node with a load circuit comprising a data detector.

Abstract: A logical transmission system includes a driver configured to receive a source data and output a first voltage at a first node; a transmission line of a characteristic impedance configured to couple the first node to a second node; a three-point three-level slicer configured to receive a second voltage at the second node and output a first ternary signal, a second ternary signal, and a third ternary in accordance with a first reference voltage, a second reference voltage, a first clock, a second clock, and a third clock; and a CDR (clock-data recovery) unit configured to receive a reference clock, the first ternary signal, the second ternary signal, and the third ternary signal and output a recovered data, the first reference voltage, the second reference voltage, the first clock, the second clock, and the third clock.

Abstract: Compositions and methods for making a plurality of probes for analyzing a plurality of nucleic acid samples are provided. Compositions and methods for analyzing a plurality of nucleic acid samples to obtain sequence information in each nucleic acid sample are also provided.

Abstract: Compositions and methods for making a plurality of probes for analyzing a plurality of nucleic acid samples are provided. Compositions and methods for analyzing a plurality of nucleic acid samples to obtain sequence information in each nucleic acid sample are also provided.

Abstract: Controlled release oral solid dosage form for the reduction of serum cholesterol levels in humans include a drug comprising an alkyl ester of hydroxy substituted naphthalenes (e.g., lovastatin) and a controlled release carrier, such that the dosage form provides a mean time to maximum plasma concentration (Tmax) of the drug which occurs at about 10 to about 32 hours after oral administration on a once-a-day basis to human patients. The dosage form provides a therapeutically effective reduction in serum cholesterol levels. Methods of reducing serum cholesterol levels in humans are also disclosed.

Abstract: Apparatus and methods are provided for an extraction circuit. In one configuration, an apparatus includes: an edge extraction circuit for receiving a first clock signal and outputting a second clock signal, wherein a duty cycle of the second clock is substantially smaller than a duty cycle of the first clock; a transistor for receiving the second clock signal and outputting a current signal; a transmission line for receiving the current signal on a first end and transmitting the current signal to a second end; a termination circuit for receiving the current signal at the second end and converting the current signal into a voltage signal; and an edge detection circuit for outputting a third clock by detecting an edge of the voltage signal. In one embodiment, the edge detection circuit comprises an inverter. In another embodiment, the edge detection circuit comprises a comparator.

Abstract: Sustained release pharmaceutical formulations comprising an antihyperglycemic drug or a pharmaceutically acceptable salt thereof are disclosed. The formulations provide therapeutic plasma levels of the antihyperglycemic drug to a human patient over a 24 hour period after administration.

Abstract: Sustained release pharmaceutical formulations comprising an antihyperglycemic drug or a pharmaceutically acceptable salt thereof are disclosed. The formulations provide therapeutic plasma levels of the antihyperglycemic drug to a human patient over a 24 hour period after administration.

Abstract: A LED light apparatus includes a conical reflection housing and a LED light source. The reflection housing has a vertex, a light opening aligning with the vertex, an inner flat reflection surface. The LED light source includes a light head alignedly pointing towards the vertex, wherein when the light head generates light a first portion of the light is accumulatively reflected by the reflection surface towards the light opening while a second portion of the light is projected towards the non-reflection arrangement to prevent the second portion of the light being reflected back to the light source for minimizing a black spot occurring at the light opening. Accordingly, the wide light pattern is refocused into a narrow beam pattern to improve the lighting efficiency. The distribution of the light output is regulated, and the heat generation is reduced.

Abstract: Sustained release pharmaceutical formulations comprising an antihyperglycemic drug or a pharmaceutically acceptable salt thereof are disclosed. The formulations provide therapeutic plasma levels of the antihyperglycemic drug to a human patient over a 24 hour period after administration.

Abstract: A LED lighting includes an illuminator and a reflection housing. The illuminator provides the light. The reflection housing receives and holds the illuminator, and patterns the light illuminated by the illuminator. The reflection housing includes an illuminator end, a linear reflection surface, and a light opening. The illuminator end, the linear reflection surface, and the light opening define a conical cavity which has a shape of right circular cone. The illuminator end is at the apex of the conical cavity, the lighting opening is at the bottom of the conical cavity with a circular shape, and the conical linear reflection surface is the lateral surface of the conical cavity.

Abstract: A LED light apparatus includes a conical reflection housing and a LED light source. The reflection housing has a vertex, a light opening aligning with the vertex, an inner flat reflection surface. The LED light source includes a light head alignedly pointing towards the vertex, wherein when the light head generates light a first portion of the light is accumulatively reflected by the reflection surface towards the light opening while a second portion of the light is projected towards the non-reflection arrangement to prevent the second portion of the light being reflected back to the light source for minimizing a black spot occurring at the light opening. Accordingly, the wide light pattern is refocused into a narrow beam pattern to improve the lighting efficiency. The distribution of the light output is regulated, and the heat generation is reduced.

Abstract: Compositions and methods for making a plurality of probes for analyzing a plurality of nucleic acid samples are provided. Compositions and methods for analyzing a plurality of nucleic acid samples to obtain sequence information in each nucleic acid sample are also provided.