Abstract: A compressor and an additional oil injection system with the compressor are disclosed. The compressor (1) has a compression chamber (11) and an exhaust port (12), wherein, the compression chamber (11) is communicated with the exhaust port (12), the compression chamber (11) has an oil inlet of the compression chamber (18), and an oil injection port of exhaust port (13) is provided at the exhaust port (12).

Abstract: A system and a method for an integrated test circuit are described. The test circuit includes an interface circuit and a test controller. The interface circuit is configured to communicate with a device under test to obtain a test scandump from a scandump storage corresponding to an internal circuit of the device. The test controller is configured to generate a test sequence to the interface to control the device and enable a simulation performed by a simulator having a design associated with the device. The test sequence includes identifying a mismatch pattern between a final scan pattern from a final scandump and a simulation pattern from the simulation. The mismatch pattern corresponds to a fault.

Abstract: A system and a method for implementing an application-specific cluster are disclosed. A first processor has a first architecture for a first functionality and is configured to perform a first sub-task of a task. A second processor has a second architecture for a second functionality and is configured to perform a second sub-task of the task. The second sub-task is different from the first sub-task. A power management circuit is configured to manage power consumption of the first and second processors according to the first and second sub-tasks, respectively. A driver is configured to perform task management for the first and second sub-tasks and control the power management circuit based on the first and the second sub-tasks.

Abstract: The present disclosure relates to compositions and methods for detection, identification, sequence analysis and quantification of biological organisms in a single amplification reaction. The disclosed method utilizes next-generation sequencing (NGS) to sequence amplified products. The present disclosure is also directed to kits containing primers specific to microbial and viral organisms, cancer, genetic disorders and forensics.

Abstract: A compressor and an additional oil injection system with the compressor are disclosed. The compressor (1) has a compression chamber (11) and an exhaust port (12), wherein, the compression chamber (11) is communicated with the exhaust port (12), the compression chamber (11) has an oil inlet of the compression chamber (18), and an oil injection port of exhaust port (13) is provided at the exhaust port (12).

Abstract: An electromagnetic coil, a mold, and an electromagnetic coil manufacturing method are provided. The electromagnetic coil includes an annular main body, and an inner peripheral wall of the annular main body comprises multiple claw poles arranged at intervals in a circumferential direction. The electromagnetic coil further includes an encapsulation layer, and the encapsulation layer is capable of encapsulating an upper annular wall, a lower annular wall, and an outer peripheral wall of the annular main body. The encapsulation layer is not disposed between the claw poles, and is formed by injection molding of a resin material. In the electromagnetic coil provided in the present invention, the encapsulation layer is not disposed between the claw poles of the inner peripheral wall of the annular main body, such that after moisture having entered the interior of the coil can be discharged therefrom within a short time.

Abstract: A gas compression system includes: a first-stage compressor head and a second-stage compressor head; an oil-gas separation vessel; and a sprayer disposed between the first-stage compressor head and the second-stage compressor head and configured to cool inter-stage compressed gas. The sprayer includes: a gas inlet configured to introduce compressed gas; an oil inlet configured to introduce compressor oil; and at least one oil-spraying opening configured to spray oil, which cools the inter-stage compressed gas. With the gas compression system, the sprayer can spray a mixture of oil and gas into the inter-stage compressed gas between the first-stage compressor head and the second-stage compressor head. Accordingly, by intelligently employing a characteristic of containing oil and gas in the scavenge line, an inter-stage heat exchange effect of the sprayer can be enhanced, thereby improving the performance of two-stage compression.

Abstract: An eletromagnetic coil, a mold, and an electromagnetic coil manufacturing method are provided. The eletromagnetic coil includes an annular main body, and an inner peripheral wall of the annular main body comprises multiple claw poles arranged at intervals in a circumferential direction. The electromagnetic coil further includes an encapsulation layer, and the encapsulation layer is capable of encapsulating an upper annular wall, a lower annular wall, and an outer peripheral wall of the annular main body. The encapsulation layer is not disposed between the claw poles, and is formed by injection molding of a resin material. In the electromagnetic coil, the encapsulation layer is not disposed between the claw poles of the inner peripheral wall of the annular main body, such that after moisture having entered the interior of the coil can be discharged therefrom within a short time.

Abstract: The present disclosure relates to methods of enzymatic treatment of double-stranded PCR amplified products for eliminating or minimizing primer-dimers in multiplex PCR reactions and for the efficient ligation of adapters. The present disclosure relates to methods and compositions that allow more efficient highly multiplex target amplification compared to conventional methods, compositions and kits by minimizing laboratory steps, eliminating primer-dimers and increasing the efficiency of adapter ligation. The disclosed methods use multiple target-specific primers for specific and selective amplification of targets in a subject's genome. The disclosed methods can be used for numerous downstream procedures and analysis, including DNA sequencing.

Abstract: Embodiments of the present disclosure provide a data buffering method, electronic device and computer-readable medium. The method includes receiving, at a first node of a network, time window information from a second node of the network, the time window information defining a time window when data is transmitted from the first node to the second node. The method further includes enabling a first clock circuit of the first node at least partly based on the time window information to provide a first clock signal for data transmission from the first node to the second node. Therefore, the power consumption at the first node can be effectively reduced.

Abstract: The present disclosure relates to a method of target enrichment and amplification of selective target regions of genomes or nucleic acid samples and further analysis by systems such as NGS. The disclosure provides methods and kits that can be used in numerous downstream procedures including DNA sequencing. The disclosed methods can be utilized to sequence the target nucleic acid sequences such as to detect the presence of genetic variations for biological assays, assessment of disease, to count copies of target regions, and to allow such target enrichment prior to sequencing.

Abstract: A method for identifying the genetic sex of Portunus trituberculatus is provided. The SNP markers provided by the present invention presents biallelic heterozygosity in male individuals, but presents homozygous allele type in female individuals, and can be detected by PCR amplification and sequencing method, HRM method or KASP method. The detection method is flexible and the results are stable. Among them, the KASP and HRM detection methods have high throughput, fast detection speed, and simple application. It provides an important tool for the breeding of all-female population of P. trituberculatus.

Abstract: The present disclosure relates to compositions and methods for detection, identification and quantification of human papillomaviruses (HPV) and clinically significant sexually transmitted infections (STI) in a single amplification reaction. The disclosed method utilizes next-generation sequencing (NGS) to sequence amplified products. The present disclosure is also directed to kits containing primers specific to multiple HPV and STI targets.

Abstract: The present invention discloses a wide angle backlight lens which consists of lens mounting plate and lens body. Further, the upper outer surface of lens body is fixedly connected with the central position of the lower outer surface of lens mounting plate. Four sets of lens stands are installed near four corners of the upper outer surface of said lens mounting plate. Each set of said lens stands consists of two assembling stands. The luminous slot (4) is installed in the central position of the lower outer surface of said lens body (2) and lamp mounting slot (5) and reflective aperture (6) are installed in the central position of the upper outer surface of said lens mounting plate (1). A wide angle backlight lens described in the present invention is available for convergence and divergence of light rays according to actual needs, to improve the range of light diffusion and luminous intensity, hence realizing a higher uniformity of flares.

Abstract: The present disclosure relates to a method for the computation of the coverage of unexplained reads in the assignment of alleles for genetic analysis.

Abstract: The present disclosure relates to methods of enzymatic treatment of double-stranded PCR amplified products for eliminating or minimizing primer-dimers in multiplex PCR reactions and for the efficient ligation of adapters. The present disclosure relates to methods and compositions that allow more efficient highly multiplex target amplification compared to conventional methods, compositions and kits by minimizing laboratory steps, eliminating primer-dimers and increasing the efficiency of adapter ligation. The disclosed methods use multiple target-specific primers for specific and selective amplification of targets in a subject's genome. The disclosed methods can be used for numerous downstream procedures and analysis, including DNA sequencing.

Abstract: The present disclosure relates to compositions and methods for detection, identification and quantification of human papillomaviruses (HPV) and clinically significant sexually transmitted infections (STI) in a single amplification reaction. The disclosed method utilizes next-generation sequencing (NGS) to sequence amplified products. The present disclosure is also directed to kits containing primers specific to multiple HPV and STI targets.

Abstract: The present invention discloses a wide angle backlight lens which consists of lens mounting plate and lens body. Further, the upper outer surface of lens body is fixedly connected with the central position of the lower outer surface of lens mounting plate. Four sets of lens stands are installed near four corners of the upper outer surface of said lens mounting plate. Each set of said lens stands consists of two assembling stands. The luminous slot (4) is installed in the central position of the lower outer surface of said lens body (2) and lamp mounting slot (5) and reflective aperture (6) are installed in the central position of the upper outer surface of said lens mounting plate (1). A wide angle backlight lens described in the present invention is available for convergence and divergence of light rays according to actual needs, to improve the range of light diffusion and luminous intensity, hence realizing a higher uniformity of flares.

Abstract: Embodiments of the present disclosure provide a data buffering method, electronic device and computer-readable medium. The method includes receiving, at a first node of a network, time window information from a second node of the network, the time window information defining a time window when data is transmitted from the first node to the second node. The method further includes enabling a first clock circuit of the first node at least partly based on the time window information to provide a first clock signal for data transmission from the first node to the second node. Therefore, the power consumption at the first node can be effectively reduced.

Abstract: The present disclosure relates to a method of target enrichment and amplification of selective target regions of genomes or nucleic acid samples and further analysis by systems such as NGS. The disclosure provides methods and kits that can be used in numerous downstream procedures including DNA sequencing. The disclosed methods can be utilized to sequence the target nucleic acid sequences such as to detect the presence of genetic variations for biological assays, assessment of disease, to count copies of target regions, and to allow such target enrichment prior to sequencing.