摘要：【中文】本发明实施例提供一种用于5G超密集网络的切换管理方法，该方法包括：对于没有上下行数据传输的处于连接状态的终端启动非活跃计时器，其中在检测到终端有上下行数据传输时停止计时；在非活跃计时器未超时的情况下，确定终端是否有切换需求；响应于终端有切换需求，判断非活跃计时器是否停止计时；在非活跃计时器未停止计时的情况下，根据终端在所述非活跃计时器超时前的数据到达概率、终端的切换代价以及状态转换代价对终端进行切换处理或者状态转换处理；在非活跃计时器停止计时的情况下，根据终端的切换代价以及状态转换代价对终端进行切换处理或者状态转换处理。本发明实施例避免了不必要的切换，减少了5G超密集网络中的切换次数及中断时延。 【EN】The embodiment of the invention provides a switching management method for a 5G ultra-dense network, which comprises the following steps: starting an inactive timer for a terminal in a connection state without uplink and downlink data transmission, wherein the time is stopped when the terminal is detected to have uplink and downlink data transmission; under the condition that the inactivity timer is not overtime, determining whether the terminal has a switching requirement; responding to a switching requirement of the terminal, and judging whether the non-active timer stops timing or not; under the condition that the inactive timer does not stop timing, carrying out switching processing or state conversion processing on the terminal according to the data arrival probability of the terminal before the inactive timer is overtime, the switching cost of the terminal and the state conversion cost; and under the condition that the inactive timer stops timing, performing switching processing or state conversion processing on the terminal according to the switching cost and the state conversion cost of the terminal. The embodiment of the invention avoids unnecessary switching and reduces the switching times and the interruption time delay in the 5G ultra-dense network.

摘要：【中文】本发明提出一种三元锂离子电池单体充电策略评价方法，基于恒流恒压充电法、阶梯充电法、脉冲充电法、间歇充电法(变电流充电&变电压充电)、线性充电法、带负脉冲充电法等多种充电策略的基础研究，对实验结果采用主成分分析法(Principal Component Analysis,PCA)进行降维统计分析，最终确定充电容量、充电时间、充电温升、能量效率四个指标作为充电策略关键影响指标的主成分。与此同时，采用归纳式学习中连续型数据的区间划分——类‑属性间的相关度极大值法进一步确定了四个指标的区间划分方法及评分细则，结果可以雷达图的形式清晰呈现，最后通过对全部指标加权平均得到该充电策略的最终评分结果。 【EN】The invention provides a ternary lithium ion battery monomer charging strategy evaluation method, which is based on the basic research of various charging strategies such as a constant-current constant-voltage charging method, a step charging method, a pulse charging method, an intermittent charging method (variable-current charging and variable-voltage charging), a linear charging method, a charging method with negative pulses and the like, and adopts a Principal Component Analysis (PCA) method to perform dimension reduction statistical Analysis on an experimental result, so that four indexes of charging capacity, charging time, charging temperature rise and energy efficiency are finally determined as Principal components of key influence indexes of the charging strategy. Meanwhile, the interval division method and the grading detailed rule of the four indexes are further determined by adopting the interval division of continuous data in inductive learning, namely a correlation degree maximum value method between class and attributes, the result can be clearly presented in a radar chart form, and finally the final grading result of the charging strategy is obtained by carrying out weighted average on all indexes.

摘要：【中文】本发明提供一种鉴定大豆RN型CMS恢复基因的CAPS标记及方法，该标记用于鉴定是否含有大豆RN型细胞质雄性不育恢复基因Rf‑rn的材料，也可应用于含Rf‑rn基因的恢复系的分子标记辅助选育。该方法包括如下步骤，提取待鉴别大豆材料基因组DNA作为扩增模板，选用二对CAPS标记的引物进行聚合酶链式反应（polymerase chain reaction，PCR）扩增。扩增的PCR产物利用限制性内切酶酶切，通过1%琼脂糖凝胶电泳对酶切产物的特定长度和数量进行观察，从而确定大豆材料是否含有恢复基因Rf‑rn及其基因型。 【EN】The invention provides a CAPS marker and a method for identifying a soybean RN type CMS restoring gene, wherein the marker is used for identifying whether the soybean RN type cytoplasmic male sterility restoring gene is containedRf‑rnThe material of (1) can also be applied to a material containingRf‑rnMolecular marker assisted breeding of gene restoring line. The method comprises the following steps of extracting the genomic DNA of the soybean material to be identified as an amplification template, and selecting two pairs of CAPS-marked primers to carry out Polymerase Chain Reaction (PCR) amplification. The amplified PCR product is cut by restriction endonuclease, and the specific length and quantity of the cut product are observed by 1% agarose gel electrophoresis, so as to determine whether the soybean material contains restoring geneRf‑rnAnd their genotype.