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To tackle the challenge of low accuracy in stock prediction within high-noise environments, this paper innovatively introduces the CED-PSO-StockNet time series model. Initially, the model decomposes raw stock data using the Complete Ensemble Empirical Mode Decomposition with Adaptive Noise (CEEMDAN) technique and reconstructs the components by estimating their frequencies via the extreme point method. This process enhances component stability and mitigates noise interference. Subsequently, an Encoder-Decoder framework equipped with an attention mechanism is employed for precise prediction of the reconstructed components, facilitating more effective extraction and utilization of data features. Furthermore, this paper utilizes an Improved Particle Swarm Optimization (IPSO) algorithm to optimize the model parameters. On the Pudong Bank dataset, through ablation experiments and comparisons with baseline models, various optimization strategies incorporated into the proposed CED-PSO-StockNet model were effectively validated. Compared to the standalone LSTM model, CED-PSO-StockNet achieved a remarkable 45.59% improvement in the R2 metric. To further assess the model's generalization capability, this paper also conducted comparative experiments on the Ping An Bank dataset, and the results underscored the significant advantages of CED-PSO-StockNet in the domain of stock prediction. [ABSTRACT FROM AUTHOR]

This study investigates the syntactic complexity of various text-types in the Czech language by analysing the mean dependency distance (MDD), a measure that quantifies the average distance between syntactic heads and their dependents within a sentence, and average sentence length (ASL). Using data from the SYN2020 corpus, a large and balanced collection of contemporary written Czech, we calculate the MDD and ASL for different text-types. Our findings reveal distinct patterns in the MDD and ASL values across genres, suggesting that syntactic complexity varies among different types of texts. We observe a clear distinction between fiction and non-fiction genres, with fiction exhibiting lower MDD and ASL values, indicating a more compact syntactic structure. Non-fiction genres, particularly scientific literature, display higher MDD and ASL values, reflecting more complex syntactic constructions. Journalistic texts, such as newspapers and magazines, fall between fiction and non-fiction in terms of MDD and ASL values. These results demonstrate the potential of MDD and ASL as quantitative measures for characterizing and differentiating text-types based on their syntactic complexity. Furthermore, our analysis contributes to a deeper understanding of the syntactic variations across diverse genres in the Czech language. [ABSTRACT FROM AUTHOR]

Background: Pathogenic copy number variants (pCNVs) are associated with fetal ultrasound anomalies, which can be efficiently identified through chromosomal microarray analysis (CMA). The primary objective of the present study was to enhance understanding of the genotype–phenotype correlation in fetuses exhibiting absent or hypoplastic nasal bones using CMA. Methods: Enrolled in the present study were 94 cases of fetuses with absent/hypoplastic nasal bone, which were divided into an isolated absent/hypoplastic nasal bone group (n = 49) and a non‐isolated group (n = 45). All pregnant women enrolled in the study underwent karyotype analysis and CMA to assess chromosomal abnormalities in the fetuses. Results: Karyotype analysis and CMA detection were successfully performed in all cases. The results of karyotype and CMA indicate the presence of 11 cases of chromosome aneuploidy, with trisomy 21 being the most prevalent among them. A small supernumerary marker chromosome (sSMC) detected by karyotype analysis was further interpreted as a pCNV by CMA. Additionally, CMA detection elicited three cases of pCNVs, despite normal findings in their karyotype analysis results. Among them, one case of Roche translocation was identified to be a UPD in chromosome 15 with a low proportion of trisomy 15. Further, a significant difference in the detection rate of pCNVs was observed between non‐isolated and isolated absent/hypoplastic nasal bone (24.44% vs. 8.16%, p <.05). Conclusion: The present study enhances the utility of CMA in diagnosing the etiology of absent or hypoplastic nasal bone in fetuses. Further, isolated cases of absent or hypoplastic nasal bone strongly suggest the presence of chromosomal abnormalities, necessitating genetic evaluation through CMA. [ABSTRACT FROM AUTHOR]

In order to obtain the quality information of Taishan black tea and provide data support for the establishment of assessment criteria for quality control of Taishan black tea, in this study, 45 samples of Taishan black tea were collected during the summer to investigate their quality characteristics. The results showed that the Taishan black tea typically exhibited a dark-brown, curly appearance and a uniform texture. The tea soup displayed a bright orange-red color. The tea was mainly described as having a fruity aroma, followed by a caramel flavor, sweet aroma, flowery flavor, and clean aroma, with a strong and enduring fragrance. The taste profile was mostly heavy and mellow or heavy and strong, with fewer samples exhibiting slight bitterness and astringency. The tea leaves were characterized by a reddish-auburn color, a soft texture, and an even appearance. The main biochemical components of the Taishan black tea fell within the following ranges: water extracts (38.65–43.35%), free amino acids (1.41–3.45%), tea polyphenols (9.80–15.05%), catechins (6.11–9.03%), and caffeine (1.65–3.05%). The phenolic acid/amino acid ratio was 2.31–6.65%. Catechins and tea polyphenols emerged as critical indicators influencing taste quality, followed by amino acids, water extracts, and caffeine. The aroma analysis identified common compounds, such as 3-methyl-butanal, 2-methyl-butanal, decanal, 2-methyl-propanal, 1-octen-3-ol, and β-ionone, in most samples. These compounds exhibited relatively high contents and high odor activity values, making them the primary contributors to the tea's aroma. This investigation into the quality of Taishan black tea offers valuable scientific insights, providing a foundation for the standardization of Taishan black tea's quality. [ABSTRACT FROM AUTHOR]

Few existing reports have investigated the copy number variants (CNVs) in fetuses with central nervous system (CNS) anomalies. To gain further insights into the genotype–phenotype relationship, we conducted chromosomal microarray analysis (CMA) to reveal the pathogenic CNVs (pCNVs) that were associated with fetal CNS anomalies. We enrolled 5,460 pregnant women with different high-risk factors who had undergone CMA. Among them, 57 subjects with fetal CNS anomalies were recruited. Of the subjects with fetal CNS anomalies, 23 were given amniocentesis, which involved karyotype analysis and CMA to detect chromosomal abnormalities. The other 34 cases only underwent CMA detection using fetal abortive tissue. In this study, we identified five cases of chromosome aneuploid and nine cases of pCNVs in the fetuses, with a chromosomal aberration detection rate of 24.56% (14/57). In the 23 cases that were given both karyotype and CMA analysis, one case with trisomy 18 was detected by karyotyping. Moreover, CMA revealed a further three cases of pCNVs, including the 1p36.33p36.31, 7q11.23, and 1q21.1q21.2 microdeletions, with a 13.04% (3/23) increase in CMA yield over the karyotype analysis. Additionally, three cases of trisomy 13, one case of trisomy 21, and six cases of pCNVs were detected in the other 34 fetuses where only CMA was performed. Furthermore, a higher chromosomal aberration detection rate was observed in the extra CNS anomaly group than in the isolated CNS anomaly group (40.91% vs 14.29%). In conclude, several pathogenic CNVs were identified in the fetuses with CNS anomalies using CMA. Among the detected CNVs, ZIC2, GNB1, and NSUN5 may be the candidate genes that responsible for fetal CNS anomalies. Our findings provides an additional reference for genetic counseling regarding fetal CNS anomalies and offers further insight into the genotype–phenotype relationship. [ABSTRACT FROM AUTHOR]

Background: The causal association between thyroid dysfunction (including hyperthyroidism and hypothyroidism) and sepsis is controversial in previous studies. Therefore, we used Mendelian randomization (MR) to explore the causal association between hyperthyroidism or hypothyroidism and the susceptibility to four distinct subtypes of sepsis (streptococcal sepsis, puerperal sepsis, asthma-associated pneumonia or sepsis, and other sepsis)., Methods: In our research, we conducted two-sample Mendelian randomization (MR) analyses utilizing publicly available genome-wide association studies (GWAS) data from Sakaue et al. and the Finnish database to investigate the potential causal associations between hyperthyroidism, hypothyroidism, and each of the four distinct subtypes of sepsis, in addition to reverse MR analyses of the positive results to examine the existence of reverse causality., Results: Genetic hypothyroidism was causally related to the development of asthma-associated pneumonia or sepsis (OR IVW : 1.097, 95% CI: 1.024 to 1.174, P = 0.008); hypothyroidism was significantly associated with the development of other sepsis (OR IVW : 1.070, 95% CI: 1.028 to 1.115, P < 0.001). In addition, sensitivity analysis substantiated the robustness of these two MR findings, with no evidence of horizontal pleiotropy observed ( P > 0.05). MR Egger regression analysis demonstrated no heterogeneity between instrumental variables (IVs). Inverse MR results confirmed no reverse causality between hypothyroidism and asthma-associated pneumonia or sepsis, or between hypothyroidism and other sepsis. The findings of this study also unveiled that there is no evidence of a causal link between hypothyroidism and the development of streptococcal sepsis or puerperal sepsis. Additionally, the research provided evidence indicating the absence of a causal relationship between hyperthyroidism and streptococcal sepsis, puerperal sepsis, asthma-associated pneumonia or sepsis, and other sepsis., Conclusions: This study identified a causal link between hypothyroidism and the occurrence of asthma-associated pneumonia or sepsis, and other sepsis, but not with the development of streptococcal sepsis and puerperal sepsis. Moreover, our findings did not reveal any causal association between hyperthyroidism and streptococcal sepsis, puerperal sepsis, asthma-associated pneumonia or sepsis, and other sepsis., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2024 Hong, Zhang, Lai, Chen, Chen and Yang.)