With the rapid development of we-media information dissemination, WeChat official accounts platform has become an important way for people to obtain health related knowledge. However, the platform information is redundant, miscellaneous, and overloaded. In order to meet the increasingly accurate and efficient knowledge service needs of users, reorganizing and aggregating document knowledge resources is effective. If we use the way of artificial recognition to filter information, it will inevitably cause huge labor and time cost, and the effect is very little in front of massive articles. This paper proposes a text summarization method for the WeChat platform based on improved TextRank that takes into account both user demands and sentence features during the summarization process. The data source crawled from the Sogou WeChat platform. The results show that the TextRank algorithm has obvious hints on the accuracy of text summarization extraction after fusing the Word2vec model. The improved TextRank method, integrating user demands and sentence features into the model, makes the results of text summarization closer to the theme of the article and more able to meet the user demand. According to the complexity of the algorithm, this method is not suitable for the automatic summarization of long or multiple documents.
Total fertilization failure (TFF), which refers to fertilization failure in all mature oocytes, accounting for 5%-10% of in vitro fertilization (IVF) cycles and 1%-3% of intracytoplasmic sperm injection (ICSI) cycles in human. In this study, we recruited three unrelated primary infertile men with repeated cycles of TFF and performed whole-exome sequencing to identify the potential pathogenic variants. We identified homozygous or compound-heterozygous variants of paternal-effect genes ACTL7A and PLCZ1 that followed a Mendelian recessive inheritance pattern. Novel homozygous nonsense variant in ACTL7A [c.C146G: p.S49*] was identified in case 1, who came from a consanguineous family. Ultrastructural observation of ACTL7A-mutated
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