Abstract: A plurality of UV patches of a three-dimensional model is divided into a primary set of the UV patches and a secondary set of the UV patches based on a patch size threshold. The UV patches of the primary set are grouped into a plurality of super-patches. Each of the plurality of super-patches includes different UV patches in the primary set that are packed together in a predefined shape. The plurality of super-patches is assembled together into a first bounding box. Poses of the plurality of super-patches are adjusted to reduce spacing between the plurality of super-patches. Gaps between the UV patches in the primary set are filled with the UV patches in the secondary set.

Abstract: Embodiments of the present disclosure provide a method, an apparatus, an electronic device, and a storage medium for data processing. The method comprises: in response to a copy trigger operation, obtaining an object to be copied, and determining a target component corresponding to the object to be copied; for each of the target component, obtaining a component object and an engine object of the target component, and determining target storage data corresponding to the target component based on the component object and the engine object, wherein the target storage data comprises a component object type field, an engine object type field, component object serialized data, and engine object serialized data; and storing the target storage data corresponding to the target component into a clipboard.

Abstract: Embodiments of the disclosure provides a method, an apparatus, an electronic device and a storage medium for object processing. The method includes: in response to a deletion triggering operation, obtaining a target object to be deleted; determining object attribute data and a data association relationship corresponding to the target object, where the data association relationship is a reference relationship between the target object and a superior object containing the target object; obtaining serialized object data by serializing the object attribute data, and storing the serialized object data; and dissolving the data association relationship, and deleting the target object.

Abstract: Aspects of the disclosure provide methods and apparatuses for mesh processing. In some examples, a method for mesh processing includes receiving an input mesh that is bounded in a bounding box. The input mesh is formed of a first plurality of vertices and a first plurality of faces that connects the first plurality of vertices. The method further includes calculating at least a first visual measure for one or more faces in the first plurality of faces. At least the first visual measure for a face is calculated according to a number of valid rays respectively at a plurality of sampling positions of the face, a valid ray at a sampling position is a ray that is traced from the sampling position to the bounding box. The method also includes performing adjustments to the input mesh to generate a repaired mesh according to at least the first visual measure.

Abstract: A method and a device for encoding or decoding based on an inter-frame prediction. The method includes steps of: determining a temporal motion vector prediction value of a to-be-processed coding unit, where the temporal motion vector prediction value is a temporal motion vector prediction value of a sub-block, a temporal motion vector of which is obtainable through prediction, in sub-blocks adjacent to the to-be-processed coding unit and/or sub-blocks in the to-be-processed coding unit; determining a motion vector residual prediction value of the to-be-processed coding unit according to the temporal motion vector prediction value; determining a motion vector of a sub-block in the to-be-processed coding unit according to the temporal motion vector prediction value and the motion vector residual prediction value and performing a motion compensation according to the motion vector of the sub-block in the to-be-processed coding unit to determine a prediction block of the to-be-processed coding unit.

Abstract: Disclosed herein are lysis reagents for lysing red blood cells, thereby releasing an analyte, such as RNA from a host or pathogen, in a form suitable for analysis. The reagent includes at least a buffer, a detergent and one or both of a chloride containing salt and an anti-coagulant. The reagent serves to lyse blood cells, protect the released analyte from degradation in the lysate, and is compatible with subsequent steps for analysis of the analyte such as target capture, amplification, detection, or sequencing.

Abstract: Disclosed herein are lysis reagents for lysing red blood cells, thereby releasing an analyte, such as RNA from a host or pathogen, in a form suitable for analysis. The reagent includes at least a buffer, a detergent and one or both of a chloride containing salt and an anti-coagulant. The reagent serves to lyse blood cells, protect the released analyte from degradation in the lysate, and is compatible with subsequent steps for analysis of the analyte such as target capture, amplification, detection, or sequencing.

Abstract: Disclosed are nucleic acid oligomers, including amplification oligomers, capture probes, and detection probes, for detection of Zika virus nucleic acid. Also disclosed are methods of specific nucleic acid amplification and detection using the disclosed oligomers, as well as corresponding reaction mixtures and kits.

Abstract: The present disclosure includes, but is not limited to, methods and systems for pooling or combining multiple samples together. Particularly, this disclosure relates to pooling and combining samples in a process and system that combines samples in a way that allows targets in the pooled sample to be analyzed/detected with a similar sensitivity and specificity as for analysis/detection of targets from the individual samples of the pool. Specifically, in some embodiments, methods herein avoid a dilution effect found in commonly used sample pooling methods that can reduce their sensitivity and limit the number of samples that can be pooled. In some embodiments, methods herein include processes to de-convolute the pool down to individual samples. Methods herein may be applicable to creating and testing pooled/combined samples for target molecules and de-convoluting pooled samples to identify an individual sample in a pool containing the target.

Abstract: Disclosed are nucleic acid oligomers, including amplification oligomers, capture probes, and detection probes, for detection of Zika virus nucleic acid. Also disclosed are methods of specific nucleic acid amplification and detection using the disclosed oligomers, as well as corresponding reaction mixtures and kits.

Abstract: Disclosed are nucleic acid oligomers, including amplification oligomers, capture probes, and detection probes, for detection of Hepatitis E Virus (HEV) nucleic acid. Also disclosed are methods of specific nucleic acid amplification and detection using the disclosed oligomers, as well as corresponding reaction mixtures and kits.

Abstract: The medical field of COVID-19 diagnosis relates to methods for detecting SARS-CoV-2 nucleic acids in a sample as well as combinations of oligomers for determining the presence or absence of SARS-CoV-2 in a Sample.

Abstract: Disclosed are nucleic acid oligomers, including amplification oligomers, capture probes, and detection probes, for detection of Hepatitis E Virus (HEV) nucleic acid. Also disclosed are methods of specific nucleic acid amplification and detection using the disclosed oligomers, as well as corresponding reaction mixtures and kits.

Abstract: Disclosed are nucleic acid oligomers, including amplification oligomers, capture probes, and detection probes, for detection of Zika virus nucleic acid. Also disclosed are methods of specific nucleic acid amplification and detection using the disclosed oligomers, as well as corresponding reaction mixtures and kits.

Abstract: Nucleic acid oligomers specific for human parvovirus genomic DNA. An assay for amplifying and detecting human parvovirus genotypes 1, 2 and 3 nucleic acid in biological specimens. Compositions for amplifying and detecting the presence of human parvovirus genotypes 1, 2 and 3 genomic DNA in human biological specimens.

Abstract: This disclosure provides oligomers, compositions, and kits for detecting and quantifying Hepatitis B virus (HBV), including different genotypes and variants thereof, and related methods and uses. In some embodiments, oligomers target the P and/or S open reading frames of HBV and are configured to provide substantially equivalent quantification of different genotypes and variants of HBV.

Abstract: Nucleic acid oligomers specific for human parvovirus genomic DNA are disclosed. An assay for amplifying and detecting human parvovirus genotypes 1, 2 and 3 nucleic acid in biological specimens is disclosed. Compositions for amplifying and detecting the presence of human parvovirus genotypes 1, 2 and 3 genomic DNA in human biological specimens are disclosed.

Abstract: Various aspects of the invention relate to compositions and methods of analyzing blood plasma, blood serum, and manufacturing pools of plasma-derived products wherein an anionic surfactant is added to an aliquot of the blood plasma, blood serum, or manufacturing pool prior to analysis, and the counterion of the anionic surfactant is not sodium ion. The anionic surfactant may be, for example, lauryl sulfate. The counterion of the anionic surfactant may be, for example, lithium ion.

Abstract: This disclosure provides oligomers, compositions, and kits for detecting and quantifying Hepatitis B virus (HBV), including different genotypes and variants thereof, and related methods and uses. In some embodiments, oligomers target the P and/or S open reading frames of HBV and are configured to provide substantially equivalent quantification of different genotypes and variants of HBV.