Abstract: In a method for statistical analysis of aggregate encrypted data with key-leakage resilience for smart grids, every user area is managed by a fog node which plays the role of data aggregation gateway and data relay. All the users' electricity consumption data sent by smart meters in the same user area are firstly aggregated by the fog node to generate a fog-level aggregate ciphertext. Then the fog node further generates a digital signature for the fog-level aggregate ciphertext and sends these data to a cloud server for long-time storage. The cloud server stores all the aggregate ciphertexts and digital signatures received from different user areas in its database, and provides data query and statistical analysis services for the control center of smart grids. On the premise of without violating users' privacy, the cloud server could provide enough information for the control center, enabling it to compute the sum, arithmetic mean and variance of all users' data in specified areas in a privacy-preserving way.

Abstract: Methods of detecting cancer or a particular type or subtype thereof in a subject and treating the cancer or particular type or subtype thereof. The detection can comprise determining fragmentation patterns of classifier cell-free deoxyribonucleic acid (cfDNA) from the subject and classifying the fragmentation patterns to identify the subject as being negative or positive for the cancer or the particular type or subtype thereof. The classifier cfDNA can comprise cfDNA corresponding to at least a portion of at least one exon of one or more classifier genes. The exon can comprise the first exons of the classifier genes. The treating can comprise the specific type of subtype of cancer that is detected.

Abstract: Involved is an isolated antigen binding protein, being capable of binding CCR8 derived from a primate animal. Further involved are a pharmaceutical composition comprising the antigen binding protein, and an application of the antigen binding protein and/or the pharmaceutical composition in the prevention and/or treatment of a tumor or a cancer.

Abstract: Provided are a blockchain data processing method and apparatus, a device, and a readable storage medium. By storing a data type information table in a relational database in advance, the data type information table is used for storing storage information of all the data types, and the storage information includes a table corresponding to the data type, a mapping relationship between the service field of the Value of the data type and a table field in the corresponding table, and a data format of the Value of the data type. A data type of the Value is determined when the Key-Value data needs to be stored; and a target table corresponding to the data type of the Value is determined and the Key-Value data is written into the target table according to the data type information table.

Abstract: The present application discloses an optical imaging lens, comprising, in order from an object side to an image side along an optical axis: a first lens having a positive refractive power; a second lens having a positive refractive power; a third lens having a negative refractive power; a fourth lens; a fifth lens having a negative refractive power; and a sixth lens having a positive refractive power, wherein a distance TTL from an object side surface of the first lens to an imaging plane of the optical imaging lens on the optical axis and an entrance pupil diameter EPD of the optical imaging lens satisfy TTL/EPD<1.9; and a total effective focal length f of the optical imaging lens satisfies 6.0 mm<f<7.5 mm.

Abstract: A gamma tuning method, apparatus, device, and storage medium and belongs to the field of display technology. The method includes: selecting a plurality of different target dimming values, and correspondingly setting, for each of the target dimming values, a same voltage gamma max power and a same voltage gamma small power; for each of the target dimming values, obtaining a gamma register value for 0 gray scale under the target dimming value according to the voltage gamma max power, the voltage gamma small power, a maximum gamma register value, and a target voltage for 0 gray scale under the target dimming value; and writing the gamma register value for 0 gray scale under the target dimming value into a gamma register of the display panel.

Abstract: A concentration gradient fluorescence calibration sheet has a glass substrate and an inorganic nano fluorescent liquid lattice disposed on a surface of the glass substrate. The inorganic nano fluorescent liquid lattice has a plurality of inorganic nano fluorescent liquid sub-lattices. Inorganic fluorescent mixed liquid droplets of each inorganic nano fluorescent liquid sub-lattice are arranged in A rows×B columns. The solution concentration of the same row of inorganic nano fluorescent liquid droplets in the inorganic nano fluorescent liquid sub-lattices is the same, and the solution concentrations of two adjacent rows of inorganic nano fluorescent liquid droplets change in multiples. The concentration gradient fluorescence calibration sheet for the laser microarray chip scanner is utilized to calibrate a scanner under test and a first row of inorganic nano fluorescent liquid droplets in the inorganic nano fluorescent liquid sub-lattices are taken as index marks.

Abstract: Methods of generating phenocopy signatures and uses thereof. The methods of generating phenocopy signatures can include determining gene expression signatures that predict the presence of mutations in training cells. Uses of the phenocopy signatures include identifying cells exhibiting the phenocopy signatures, identifying subjects comprising cells that exhibit the phenocopy signatures, methods of using the phenocopy signatures to predict cells sensitive to treatment with drugs, methods of treating cells with phenocopy signatures predicted to be sensitive to treatment with drugs, methods of using phenocopy signatures to predict subjects sensitive to treatment with drugs, and methods of treating subjects with phenocopy signatures predicted to be sensitive to treatment with drugs.

Abstract: Methods of generating linear regression predictor models capable of predicting responses of patients afflicted with diseases to treatments, methods of using the linear regression predictor models to predict the responses of the patients to the treatments, and methods of administering the treatments to the patients.

Abstract: The present disclosure provides a display assembly and a display device, the display assembly includes: a flexible display panel including a first display area, a second display area and a bending area formed between the first display area and the second display area, a metal resilient member fixedly attached to one side of the flexible display panel, a metal support located on a side, away from the flexible display panel, of the metal resilient member, a first conductive adhesive structure located at the edge of the bending area and connecting the first support part and the metal resilient member, and a second conductive adhesive structure located at the edge of the bending area and connecting the second support part with the metal resilient member, wherein the metal support is fixedly attached to the metal resilient member by an adhesive layer.

Abstract: A display substrate, includes: a display region. The display region includes a plurality of sub-pixels disposed on a substrate, a plurality of first signal lines extending in a first direction, and a plurality of data lines extending in a second direction. At least one sub-pixel includes a driving circuit, and the driving circuit includes a plurality of transistors and at least one storage capacitor. The transistor at least includes a first conductive layer and a second conductive layer. The plurality of first signal lines is located in a third conductive layer. The third conductive layer is located on a side of a control electrode of a transistor of the driving circuit away from the substrate.

Abstract: A display substrate and a display device. The display substrate includes a base substrate and a plurality of sub-pixels on the base substrate, each sub-pixel includes a pixel circuit, and the pixel circuit includes a drive sub-circuit and a first reset sub-pixel. The first reset sub-pixel is configured to apply a first reset voltage to a control terminal of the drive sub-circuit in response to a first reset control voltage; the display substrate further comprises a first reset signal line electrically connected with the first terminal of the first reset sub-circuit to provide the first reset voltage, and the first reset signal line is in a semiconductor layer and comprises a doped semiconductor material.

Abstract: The present invention provides a fractional order sliding mode synchronous control method for a teleoperation system based on an event trigger mechanism. The method comprises: establishing a dynamics model for the teleoperation system by considering external disturbance and parameter uncertainty, selecting a master robot and a slave robot, interactively establishing the teleoperation system through a communication network, determining system parameters of the dynamics model, designing a fractional order nonsingular rapid terminal sliding mode surface equation by utilizing a position tracking error and a fractional order calculus, setting a trigger event condition of information interaction between the master robot and the slave robot, designing a self-adaptive fractional order nonsingular rapid terminal sliding mode controller based on the sliding mode, designing a Lyapunov function to carry out stability analysis, proving the boundedness of a closed-loop state signal of the system.

Abstract: A die steel with a high thermal diffusion coefficient includes 0.30-0.40 wt. % of C, 0.05-0.10 wt. % of Si, 2.50-3.40 wt. % of Mo, 0.01-0.05 wt. % of Nb, 0.30-0.50 wt. % of Co, 0.01-0.05 wt. % of RE, the rest is Fe and unavoidable impurities, wherein in the die steel, P?0.15 wt. %, S?0.025 wt. %. A preparation method of the die steel includes steps of melting, electroslag remelting, electroslag ingot annealing, forging, spheroidizing annealing, quenching and tempering.

Abstract: A display substrate and a drive method thereof and a display device. The display substrate includes a base substrate and a plurality of sub-pixels on the base substrate, each sub-pixel includes a pixel circuit, and the pixel circuit includes a first reset sub-pixel. The first reset sub-pixel is configured to apply a first reset voltage to a light-emitting element in response to a first reset control voltage to reversely bias the light-emitting element.

Abstract: The embodiments of the present disclosure provide an array substrate and a related display panel and a related display device. An array substrate includes a plurality of pairs of scan signal lines. A first scan signal line of the m-th pair of scan signal lines is configured to provide a first scan signal to a sub-pixel in a (2n?1)-th column from sub-pixels in the m-th. And a plurality of pairs of driving reset control signal lines. A second driving reset control signal line of the m-th pair of driving reset control signal lines is configured to provide a second driving reset control signal to the sub-pixel in the 2n-th column from the sub-pixels in the m-th row. The m and n are integers greater than or equal to 1. In the embodiments of the present disclosure, the first scan signal line of the m-th pair of scan signal lines and the second driving reset control signal line of the m-th pair of driving reset control signal lines are the same signal line.

Abstract: Various embodiments of the teachings herein include a method for optimizing a gasifier model. Some examples include: virtually partitioning the gasifier by temperature; enabling the gasifier model to input feed split from total feed based on a respective proportion coefficient in each virtual partition to perform gasification reactions independently by each virtual partition; enabling the gasifier model to determine a virtual value of a gasifier parameter after mixing the virtual partitions, quenching and shifting when gasification reactions reach an equilibrium in each virtual partition; determining a measured value of the gasifier parameter when the total feed is input; and adjusting the proportion coefficients based on a comparison result between the measured value and the virtual value of the gasifier parameter.

Abstract: The present disclosure provides antibodies that bind to OX40 and antigen binding fragments thereof, and use of the antibodies and the antigen binding fragments in the treatment of diseases for example cancers. The antibodies or the antigen binding fragments include a heavy chain variable region including one or more CDRs having an amino acid sequence selected from amino acid sequences as set forth in SEQ ID NOs: 1-12.

Abstract: A display substrate, including: a display region and a peripheral region located on the periphery of the display region. A scan driver circuit is disposed in the peripheral region. A plurality of sub-pixels, and a plurality of first signal lines that are connected to the scan driver circuit and extend in a first direction, are disposed in the display region. The display region includes: a substrate, and a semiconductor layer, a first conductive layer, a second conductive layer and a third conductive layer that are sequentially disposed on the substrate. The third conductive layer comprises: a plurality of first signal lines, and first electrodes and second electrodes of a plurality of transistors. An insulating layer between the third conductive layer and the first conductive layer is provided with first via holes.

Abstract: Methods of generating phenocopy signatures and uses thereof. The methods of generating phenocopy signatures can include determining gene expression signatures that predict the presence of mutations in training cells. Uses of the phenocopy signatures include identifying cells exhibiting the phenocopy signatures, identifying subjects comprising cells that exhibit the phenocopy signatures, methods of using the phenocopy signatures to predict cells sensitive to treatment with drugs, methods of treating cells with phenocopy signatures predicted to be sensitive to treatment with drugs, methods of using phenocopy signatures to predict subjects sensitive to treatment with drugs, and methods of treating subjects with phenocopy signatures predicted to be sensitive to treatment with drugs.