Abstract: An image processing method, apparatus, and an electronic device. The method includes: adjusting an original luminance parameter of a pixel point in an image based on a luminance adjustment strategy to obtain an adjusted luminance parameter; determining a luminance change parameter of the pixel point according to the original luminance parameter and the adjusted luminance parameter, where the luminance change parameter is configured to represent a changing degree of the adjusted luminance parameter relative to the original luminance parameter; and adjusting an original saturation parameter of the pixel point based on the luminance change parameter to obtain an adjusted saturation parameter, so as to compensate for a saturation of the pixel point.

Abstract: The present disclosure belongs to the technical field of board manufacturing, and relates to a method for preparing a weather-resistant printing board. It specifically includes the following steps: S-1, printing on at least one decorative surface of a core material layer of the board or on an overlay surface of a prefabricated wear-resistant layer to form a printed pattern layer; S-2, forming an adhesive layer between the printed pattern layer and the prefabricated wear-resistant layer or between the printed pattern layer and the core material layer; S-3, bonding the prefabricated wear-resistant layer and the core material layer to obtain the board. The peeling force of the wear-resistant layer of the outer layer of the board obtained by the present disclosure can reach at least 3 MPa, and at the same time, the prefabricated wear-resistant layer is adopted to reduce the requirements on device and production sites.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present disclosure belongs to the technical field of board manufacturing, and relates to a method for preparing a weather-resistant printing board. It specifically includes the following steps: S-1, printing on at least one decorative surface of a core material layer of the board or on an overlay surface of a prefabricated wear-resistant layer to form a printed pattern layer; S-2, forming an adhesive layer between the printed pattern layer and the prefabricated wear-resistant layer or between the printed pattern layer and the core material layer; S-3, bonding the prefabricated wear-resistant layer and the core material layer to obtain the board. The peeling force of the wear-resistant layer of the outer layer of the board obtained by the present disclosure can reach at least 3 MPa, and at the same time, the prefabricated wear-resistant layer is adopted to reduce the requirements on device and production sites.

Abstract: The disclosure relates to a foamed floor with wood texture. It belongs to the technical field of co-extruded foam plate. It includes a foam matrix and a hard surface layer including (a) and (b); (a): a first exposed surface, a connecting substrate and a base layer formed by the first color resin; (b): a second exposed surface and a connecting substrate formed by the second color resin. The first exposed surface is composed of a plurality of exposed units, and the second exposed surface is composed of a plurality of sunken units. The exposed units and the sunken units are arranged alternately. A connecting unit is arranged between the adjacent exposed unit and the sunken unit, and it's composed of the connecting substrate and a connecting profile. The disclosure uses resin as a material, is based on two surface layers, and realizes the realistic effect of wood texture through some levels of expressions such as three-dimensional (depth of texture), color difference, brightness etc.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present invention provides methods of determining the size of a particular nucleic acid segment of interest in a sample of nucleic acids through fragmentation of DNA, size fractionation, an optional second fragmentation, and identification using a marker sequence. In particular aspects, an expansion or reduction of tandem repeat sequences can be detected. In further aspects, carriers and individuals afflicted with fragile X syndrome or other diseases associated with tandem repeats can be distinguished from normal individuals.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present invention provides methods of determining the size of a particular nucleic acid segment of interest in a sample of nucleic acids through fragmentation of DNA, size fractionation, an optional second fragmentation, and identification using a marker sequence. In particular aspects, an expansion or reduction of tandem repeat sequences can be detected. In further aspects, carriers and individuals afflicted with fragile X syndrome or other diseases associated with tandem repeats can be distinguished from normal individuals.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.

Abstract: The present invention provides novel mutations of the CFTR gene related to cystic fibrosis or to conditions associated with cystic fibrosis. Also provided are probes for detecting the mutant sequences. Methods of identifying if an individual has a genotype containing one or more mutations in the CFTR gene are further provided.