期刊文献+
共找到206篇文章
< 1 2 11 >
每页显示 20 50 100
Analysis on the Influence of Automatic Station Temperature Data on the Sequence Continuity of Historical Meteorological Data 被引量:1
1
作者 CHEN Ming1, GAI Xiao-bo2, FAN Xin-yu1, SONG Min1 1. Jinzhou Meteorology Bureau in Liaoning Province, Jinzhou 121001, China 2. Dalian Meteorological Bureau in Liaoning Province, Dalian 116001, China 《Meteorological and Environmental Research》 CAS 2011年第4期12-14,17,共4页
[Objective] The research aimed to study the influence of automatic station data on the sequence continuity of historical meteorological data. [Method] Based on the temperature data which were measured by the automatic... [Objective] The research aimed to study the influence of automatic station data on the sequence continuity of historical meteorological data. [Method] Based on the temperature data which were measured by the automatic meteorological station and the corresponding artificial observation data during January-December in 2001, the monthly average, maximum and minimum temperatures in the automatic station were compared with the corresponding artificial observation temperature data in the parallel observation period by using the contrast difference and the standard deviation of difference value. The difference between the automatic station and the artificial data, the variation characteristics were understood. Meanwhile, the significance test and analysis of annual average value were carried out by the data sequence during 1990-2009. The influence of automatic station replacing the artificial observation on the sequence continuity of historical temperature data was discussed. [Result] Although the two temperature data in the parallel observation period had the certain difference, the difference was in the permitted range of automatic station difference value on average. The difference of individual month surpassed the permitted range of automatic station difference value. The significance test showed that the annual average temperature and the annual average minimum temperature which were observed in the automatic station had the difference with the historical data. It had the certain influence on the annual temperature sequence, but the difference wasn’t significant as a whole. When the automatic observation combined with the artificial observation to use, the sequence needed carry out the homogeneous test and correction. [Conclusion] The research played the important role on guaranteeing the monorail running of automatic station, optimizing the meteorological surface observation system, improving the climate sequence continuity of meteorological element and the reliability of climate statistics. 展开更多
关键词 Automatic observation Artificial observation data sequence analysis China
在线阅读 下载PDF
High-throughput Sequencing Technology and Its Application 被引量:11
2
作者 Zhu Qiang-long Liu Shi +1 位作者 Gao Peng Luan Fei-shi 《Journal of Northeast Agricultural University(English Edition)》 CAS 2014年第3期84-96,共13页
Gene sequencing is a great way to interpret life, and high-throughput sequencing technology is a revolutionary technological innovation in gene sequencing researches. This technology is characterized by low cost and h... Gene sequencing is a great way to interpret life, and high-throughput sequencing technology is a revolutionary technological innovation in gene sequencing researches. This technology is characterized by low cost and high-throughput data. Currently, high-throughput sequencing technology has been widely applied in multi-level researches on genomics, transcriptomics and epigenomics. And it has fundamentally changed the way we approach problems in basic and translational researches and created many new possibilities. This paper presented a general description of high-throughput sequencing technology and a comprehensive review of its application with plain, concisely and precisely. In order to help researchers finish their work faster and better, promote science amateurs and understand it easier and better. 展开更多
关键词 high-throughput sequencing data analysis genome sequence transcriptome sequence BIOINFORMATICS
在线阅读 下载PDF
A Comprehensive Review on RNA-seq Data Analysis 被引量:1
3
作者 Zhang Li Liu Xuejun 《Transactions of Nanjing University of Aeronautics and Astronautics》 EI CSCD 2016年第3期339-361,共23页
RNA-sequencing(RNA-seq),based on next-generation sequencing technologies,has rapidly become a standard and popular technology for transcriptome analysis.However,serious challenges still exist in analyzing and interpre... RNA-sequencing(RNA-seq),based on next-generation sequencing technologies,has rapidly become a standard and popular technology for transcriptome analysis.However,serious challenges still exist in analyzing and interpreting the RNA-seq data.With the development of high-throughput sequencing technology,the sequencing depth of RNA-seq data increases explosively.The intricate biological process of transcriptome is more complicated and diversified beyond our imagination.Moreover,most of the remaining organisms still have no available reference genome or have only incomplete genome annotations.Therefore,a large number of bioinformatics methods for various transcriptomics studies are proposed to effectively settle these challenges.This review comprehensively summarizes the various studies in RNA-seq data analysis and their corresponding analysis methods,including genome annotation,quality control and pre-processing of reads,read alignment,transcriptome assembly,gene and isoform expression quantification,differential expression analysis,data visualization and other analyses. 展开更多
关键词 transcriptome analysis high-throughput sequencing RNA-seq data analysis analysis pipeline
在线阅读 下载PDF
Identification of distant co-evolving residues in antigen 85C from Mycobacterium tuberculosis using statistical coupling analysis of the esterase family proteins 被引量:2
4
作者 Veeky Baths Utpal Roy 《The Journal of Biomedical Research》 CAS 2011年第3期165-169,共5页
A fundamental goal in cellular signaling is to understand allosteric communication, the process by which sig-nals originating at one site in a protein propagate reliably to affect distant functional sites. The general... A fundamental goal in cellular signaling is to understand allosteric communication, the process by which sig-nals originating at one site in a protein propagate reliably to affect distant functional sites. The general principles of protein structure that underlie this process remain unknown. Statistical coupling analysis (SCA) is a statistical technique that uses evolutionary data of a protein family to measure correlation between distant functional sites and suggests allosteric communication. In proteins, very distant and small interactions between collections of amino acids provide the communication which can be important for signaling process. In this paper, we present the SCA of protein alignment of the esterase family (pfam ID: PF00756) containing the sequence of antigen 85C secreted by Mycobacterium tuberculosis to identify a subset of interacting residues. Clustering analysis of the pairwise correlation highlighted seven important residue positions in the esterase family alignments. These resi-dues were then mapped on the crystal structure of antigen 85C (PDB ID: 1DQZ). The mapping revealed corre-lation between 3 distant residues (Asp38, Leu123 and Met125) and suggests allosteric communication between them. This information can be used for a new drug against this fatal disease. 展开更多
关键词 antigen 85C Mycobacterium tuberculosis clustering analysis COVARIANCE statistical coupling analy-sis esterase family multiple sequence alignments PFAM Protein data Bank.
暂未订购
Surveillance of emerging SARS-CoV-2 variants by nanopore technology-based genome sequencing 被引量:1
5
作者 J.I.Abeynayake G.P.Chathuranga +1 位作者 M.A.Y.Fernando M.K.Sahoo 《Asian Pacific Journal of Tropical Medicine》 SCIE CAS 2023年第7期313-320,共8页
Objective:To surveill emerging variants by nanopore technology-based genome sequencing in different COVID-19 waves in Sri Lanka and to examine the association with the sample characteristics,and vaccination status.Met... Objective:To surveill emerging variants by nanopore technology-based genome sequencing in different COVID-19 waves in Sri Lanka and to examine the association with the sample characteristics,and vaccination status.Methods:The study analyzed 207 RNA positive swab samples received to sequence laboratory during different waves.The N gene cut-off threshold of less than 30 was considered as the major inclusion criteria.Viral RNA was extracted,and elutes were subjected to nanopore sequencing.All the sequencing data were uploaded in the publicly accessible database,GISAID.Results:The Omicron,Delta and Alpha variants accounted for 58%,22%and 4%of the variants throughout the period.Less than 1%were Kappa variant and 16%of the study samples remained unassigned.Omicron variant was circulated among all age groups and in all the provinces.Ct value and variants assigned percentage was 100%in Ct values of 10-15 while only 45%assigned Ct value over 25.Conclusions:The present study examined the emergence,prevalence,and distribution of SARS-CoV-2 variants locally and has shown that nanopore technology-based genome sequencing enables whole genome sequencing in a low resource setting country. 展开更多
关键词 Emerging SARS-CoV-2 variants Laboratory surveillance Nanopore technology Genome sequencing Bioinformatics analysis and phylogeny Sociodemographic and sample cutoff(Ct)threshold Global sharing of genomic data/GISAID
暂未订购
Next generation sequencing for profiling expression of miRNAs: technical progress and applications in drug development
6
作者 Jie Liu Steven F. Jennings +1 位作者 Weida Tong Huixiao Hong 《Journal of Biomedical Science and Engineering》 2011年第10期666-676,共11页
miRNAs are non-coding RNAs that play a regulatory role in expression of genes and are associated with diseases. Quantitatively measuring expression levels of miRNAs can help understanding the mechanisms of human disea... miRNAs are non-coding RNAs that play a regulatory role in expression of genes and are associated with diseases. Quantitatively measuring expression levels of miRNAs can help understanding the mechanisms of human diseases and discovering new drug targets. There are three major methods that have been used to measure the expression levels of miRNAs: real-time reverse transcription PCR (qRT-PCR), microarray, and the newly introduced next-generation sequencing (NGS). NGS is not only suitable for profiling of known miRNAs that qRT-PCR and microarray can do too but also able to detect unknown miRNAs that the other two methods are incapable. Profiling of miRNAs by NGS has been progressed rapidly and is a promising field for applications in drug development. This paper will review the technical advancement of NGS for profiling miRNAs, including comparative analyses between different platforms and software packages for analyzing NGS data. Examples and future perspectives of applications of NGS profiling miRNAs in drug development will be discussed. 展开更多
关键词 MIRNAS Next-Generation sequencing EXPRESSION data analysis Drug Development
暂未订购
Next-generation sequencing for clinical HLA typing
7
作者 Chengyu Wu Qiang Shi +1 位作者 Dinh Pham Afzal Nikaein 《实用器官移植电子杂志》 2018年第4期275-285,共11页
下一代测序(NGS)已经被证明可有效的减少人类白细胞抗原(HLA)分型的不准确性和检测成本,同时还可以检测出之前未测序的HLA基因的详细信息。本研究介绍了在Illumina公司的Mi Seq平台上使用NGS开发的HLA分型测定的性能要求。共纳入288个样... 下一代测序(NGS)已经被证明可有效的减少人类白细胞抗原(HLA)分型的不准确性和检测成本,同时还可以检测出之前未测序的HLA基因的详细信息。本研究介绍了在Illumina公司的Mi Seq平台上使用NGS开发的HLA分型测定的性能要求。共纳入288个样品,其之前以HLA-A,HLA-B,HLA-C,HLA-DRB1,HLA-DQA/B和HLA-DPA/B为特征,其使用Sanger测序、序列特异性引物和序列特异性寡核苷酸技术进行高分辨率的分型。这些样本携带高比例HLA特异性的等位基因。测序数据使用Omixon的HLA TwinTM进行分析。评估等位基因平衡、敏感性、特异性、精确性、准确性和不准确性。这些结果证明了NGS对HLA分型的可行性和获益处,因为这项技术非常准确,几乎排除了所有的不确定性,为HLA基因长度提供了完整的测序信息,并形成了利用单一方法进行HLA分型的基础免疫遗传学实验室。 展开更多
关键词 HLA分型 下一代测序 全基因组Illumina数据分析 临床应用
暂未订购
Cytokine storm promoting T cell exhaustion in severe COVID-19 revealed by single cell sequencing data analysis
8
作者 Minglei Yang Chenghao Lin +4 位作者 Yanni Wang Kang Chen Yutong Han Haiyue Zhang Weizhong Li 《Precision Clinical Medicine》 2022年第2期87-99,共13页
Background:Evidence has suggested that cytokine storms may be associated with T cell exhaustion(TEX)in COVID-19.However,the interaction mechanism between cytokine storms and TEX remains unclear.Methods:With the aim of... Background:Evidence has suggested that cytokine storms may be associated with T cell exhaustion(TEX)in COVID-19.However,the interaction mechanism between cytokine storms and TEX remains unclear.Methods:With the aim of dissecting the molecular relationship of cytokine storms and TEX through single-cell RNA sequencing data analysis,we identified 14 cell types from bronchoalveolar lavage fluid of COVID-19 patients and healthy people.We observed a novel subset of severely exhausted CD8 T cells(Exh T_CD8)that co-expressed multiple inhibitory receptors,and two macrophage subclasses that were the main source of cytokine storms in bronchoalveolar.Results:Correlation analysis between cytokine storm level and TEX level suggested that cytokine storms likely promoted TEX in severe COVID-19.Cell–cell communication analysis indicated that cytokines(e.g.CXCL10,CXCL11,CXCL2,CCL2,and CCL3)released by macrophages acted as ligands and significantly interacted with inhibitory receptors(e.g.CXCR3,DPP4,CCR1,CCR2,and CCR5)expressed by Exh T_CD8.These interactions formed the cytokine–receptor axes,which were also verified to be significantly correlated with cytokine storms and TEX in lung squamous cell carcinoma.Conclusions:Cytokine storms may promote TEX through cytokine-receptor axes and be associated with poor prognosis in COVID19.Blocking cytokine-receptor axes may reverse TEX.Our finding provides novel insights into TEX in COVID-19 and new clues for cytokine-targeted immunotherapy development. 展开更多
关键词 COVID-19 immune exhaustion cytokine storm single-cell sequencing data analysis T cell immune checkpoint
原文传递
High-throughput phenotyping: Breaking through the bottleneck in future crop breeding 被引量:15
9
作者 Peng Song Jinglu Wang +2 位作者 Xinyu Guo Wanneng Yang Chunjiang Zhao 《The Crop Journal》 SCIE CSCD 2021年第3期633-645,共13页
With the rapid development of genetic analysis techniques and crop population size,phenotyping has become the bottleneck restricting crop breeding.Breaking through this bottleneck will require phenomics,defined as the... With the rapid development of genetic analysis techniques and crop population size,phenotyping has become the bottleneck restricting crop breeding.Breaking through this bottleneck will require phenomics,defined as the accurate,high-throughput acquisition and analysis of multi-dimensional phenotypes during crop growth at organism-wide levels,ranging from cells to organs,individual plants,plots,and fields.Here we offer an overview of crop phenomics research from technological and platform viewpoints at various scales,including microscopic,ground-based,and aerial phenotyping and phenotypic data analysis.We describe recent applications of high-throughput phenotyping platforms for abiotic/biotic stress and yield assessment.Finally,we discuss current challenges and offer perspectives on future phenomics research. 展开更多
关键词 high-throughput phenotyping Crop breeding Crop phenomics Phenotyping platform data analysis
在线阅读 下载PDF
Integrating artificial intelligence and high-throughput phenotyping for crop improvement 被引量:1
10
作者 Mansoor Sheikh Farooq Iqra +3 位作者 Hamadani Ambreen Kumar A Pravin Manzoor Ikra Yong Suk Chung 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2024年第6期1787-1802,共16页
Crop improvement is crucial for addressing the global challenges of food security and sustainable agriculture.Recent advancements in high-throughput phenotyping(HTP)technologies and artificial intelligence(AI)have rev... Crop improvement is crucial for addressing the global challenges of food security and sustainable agriculture.Recent advancements in high-throughput phenotyping(HTP)technologies and artificial intelligence(AI)have revolutionized the field,enabling rapid and accurate assessment of crop traits on a large scale.The integration of AI and machine learning algorithms with HTP data has unlocked new opportunities for crop improvement.AI algorithms can analyze and interpret large datasets,and extract meaningful patterns and correlations between phenotypic traits and genetic factors.These technologies have the potential to revolutionize plant breeding programs by providing breeders with efficient and accurate tools for trait selection,thereby reducing the time and cost required for variety development.However,further research and collaboration are needed to overcome the existing challenges and fully unlock the power of HTP and AI in crop improvement.By leveraging AI algorithms,researchers can efficiently analyze phenotypic data,uncover complex patterns,and establish predictive models that enable precise trait selection and crop breeding.The aim of this review is to explore the transformative potential of integrating HTP and AI in crop improvement.This review will encompass an in-depth analysis of recent advances and applications,highlighting the numerous benefits and challenges associated with HTP and AI. 展开更多
关键词 artificial intelligence crop improvement data analysis high-throughput phenotyping machine learning precision agriculture trait selection
在线阅读 下载PDF
Long-term V(RI) CCD photometry of pre-main-sequence stars in the association Cepheus OB3
11
作者 Sunay Ibryamov Gabriela Zidarova +1 位作者 Evgeni Semkov Stoyanka Peneva 《Research in Astronomy and Astrophysics》 SCIE CAS CSCD 2021年第8期91-98,共8页
Results from optical CCD photometric observations of 13 pre-main-sequence stars collected during the period from February 2007 to November 2020 are presented.These stars are located in the association Cepheus OB3,in t... Results from optical CCD photometric observations of 13 pre-main-sequence stars collected during the period from February 2007 to November 2020 are presented.These stars are located in the association Cepheus OB3,in the field of the young star V733 Cephei.Photometric observations,especially concerning the long-term variability of the stars,are missing in the literature.We present the first longterm V(RI)c monitoring for them,that cover 13 years.Results from our study indicate that all of the investigated stars manifest strong photometric variability.The presented paper is a part of our program for the photometric study of pre-main-sequence stars located in active star-forming regions. 展开更多
关键词 stars:pre-main sequence stars:variables:T Tauri Herbig Ae/Be techniques:photometric methods:observational data analysis stars:individual
在线阅读 下载PDF
临床基因组测序解读与报告专家共识
12
作者 卢宇蓝 李国壮 +31 位作者 王雅琼 徐可欣 董欣然 蔡继昊 吴冰冰 王慧君 方萍 王剑 王华 孙路明 叶勇裕 李晴 刘雅萍 刘丽 刘宁 刘嘉琦 宋昉 杨琳 邱正庆 陈泽夫 罗华夏 郭丹 郝婵娟 赵森 黄尚志 彭镜 蔡小强 睢瑞芳 李林康 吴南 周文浩 张抒扬 《遗传》 北大核心 2025年第3期314-328,共15页
基因组测序(genome sequencing,GS)是一种全面且系统地检测个体核基因组和线粒体基因组DNA序列的技术,旨在识别遗传变异并研究这些变异在人类健康和疾病发生发展中的作用。作为一种应用越来越广泛的检测技术,GS凭借高通量、高准确性和... 基因组测序(genome sequencing,GS)是一种全面且系统地检测个体核基因组和线粒体基因组DNA序列的技术,旨在识别遗传变异并研究这些变异在人类健康和疾病发生发展中的作用。作为一种应用越来越广泛的检测技术,GS凭借高通量、高准确性和全面性的优势,为临床诊断提供了重要支持。然而,其复杂的数据分析与解读对专业知识和经验提出了较高要求,也带来了诸多挑战。运用GS技术进行遗传病分子诊断会涉及临床应用的伦理与技术问题,包括知情同意、诊断性数据解读、报告范围和内容等。本专家共识总结了临床基因组测序(clinical GS,c GS)的核心流程,明确了检测范围与技术局限性,提供了数据质控、分析、注释及变异解读的关键步骤,并对报告内容和知情同意的争议性问题展开讨论。本共识旨在帮助相关从业人员正确理解和规范使用临床基因组测序技术,提升遗传病诊断的准确性,优化技术的临床效用,推动医学科学研究的进步。 展开更多
关键词 遗传罕见病 基因组测序 高通量测序数据分析 变异解读 遗传检测报告
暂未订购
Dissecting the cell microenvironment of ovarian endometrioma through single-cell RNA sequencing 被引量:2
13
作者 Jiangpeng Wu Siyu Xia +12 位作者 Wenting Ye Yan Sun Jing Cai Fubing Yu Haiping Wen Xiuwei Yi Taikang Li Mingwei Chen Jiayun Chen Ge Song Chuanbin Yang Yali Song Jigang Wang 《Science China(Life Sciences)》 2025年第1期116-129,共14页
Ovarian endometrioma(OE),also known as“chocolate cysts,”is a cystic mass that develops in the ovaries due to endometriosis and is a common gynecological condition characterized by the growth of endometrial tissue ou... Ovarian endometrioma(OE),also known as“chocolate cysts,”is a cystic mass that develops in the ovaries due to endometriosis and is a common gynecological condition characterized by the growth of endometrial tissue outside the uterus,leading to symptoms such as dysmenorrhea,pelvic pain,and infertility.However,the precise molecular and cellular mechanisms driving this pathophysiology remain largely unknown,posing challenges for diagnosis and treatment.Here,we employed integrated single-cell transcriptomic profiling of over 52,000 individual cells from endometrial tissues of OE patients and healthy donors and identified twelve major cell populations.We identified notable alterations in cell type-specific proportions and molecular signatures associated with OE.Notably,the activation of IGFBP5^(+) macrophages with pro-inflammatory properties,NK cell exhaustion,and aberrant proliferation of IQCG^(+) and KLF2^(+) epithelium are key features and may be the potential mechanisms underlying the pathogenesis of OE.Collectively,our data contribute to a better understanding of OE at the single cell level and may pave the way for the development of novel therapeutic strategies. 展开更多
关键词 OVARY high-throughput sequencing TRANSCRIPTOMICS gene expression analysis ligand-receptor analysis
暂未订购
Critical role of bioinformatics in translating huge amounts of next-generation sequencing data into personalized medicine 被引量:7
14
作者 HONG HuiXiao ZHANG WenQian +6 位作者 SHEN Jie SU ZhenQiang NING BaiTang HAN Tao PERKINS Roger SHI LeMing TONG WeiDa 《Science China(Life Sciences)》 SCIE CAS 2013年第2期110-118,共9页
Realizing personalized medicine requires integrating diverse data types with bioinformatics.The most vital data are genomic information for individuals that are from advanced next-generation sequencing(NGS) technologi... Realizing personalized medicine requires integrating diverse data types with bioinformatics.The most vital data are genomic information for individuals that are from advanced next-generation sequencing(NGS) technologies at present.The technologies continue to advance in terms of both decreasing cost and sequencing speed with concomitant increase in the amount and complexity of the data.The prodigious data together with the requisite computational pipelines for data analysis and interpretation are stressors to IT infrastructure and the scientists conducting the work alike.Bioinformatics is increasingly becoming the rate-limiting step with numerous challenges to be overcome for translating NGS data for personalized medicine.We review some key bioinformatics tasks,issues,and challenges in contexts of IT requirements,data quality,analysis tools and pipelines,and validation of biomarkers. 展开更多
关键词 personalized medicine next-generation sequencing BIOINFORMATICS short reads ALIGNMENT ASSEMBLE data analysis
暂未订购
基于单细胞测序数据探索阿尔茨海默病的发病机制
15
作者 任彦学 赵琳琳 +4 位作者 何敏 于倩 汪煜楠 黄山 张惊宇 《中国实验诊断学》 2025年第6期634-642,共9页
目的应用单细胞测序技术探索阿尔茨海默病的发病机制。方法从单细胞转录组数据库下载疾病组及对照组数据,下载后进行数据质控,利用Seurat软件进行数据整合、聚类,利用T-分布随机邻域嵌入和一致流形逼近与投影软件进行图的可视化。利用Si... 目的应用单细胞测序技术探索阿尔茨海默病的发病机制。方法从单细胞转录组数据库下载疾病组及对照组数据,下载后进行数据质控,利用Seurat软件进行数据整合、聚类,利用T-分布随机邻域嵌入和一致流形逼近与投影软件进行图的可视化。利用SingleR与人工检查的综合方式完成细胞注释,最后将进一步进行基因差异分析、拟时序分析、细胞间通讯分析。结果细胞图谱构建结果显示:疾病组细胞类型为中性粒细胞、小胶质细胞、神经元以及星形胶质细胞。对照组细胞类型为神经元与星形胶质细胞;基因表达差异结果显示:CD74、B2M、SPP1、NEAT等基因在两组数据中均差值较为显著;拟时序分析结果显示:疾病组中神经元分布不均,对照组中的神经元均匀分布,星形胶质细胞则是相反的结果。细胞间通讯分析显示:在疾病组中神经元与其他细胞类型的细胞间通讯较弱,而星形胶质细胞细胞与其他细胞通讯作用强,小胶质细胞与其他细胞也有着若干受体配体对以及信号转导通路。并且小胶质细胞与星形胶质细胞通过SPP1信号通路进行细胞间相互作用的数量多。结论本研究通过单细胞测序技术得知在疾病组CD74、B2M、SPP1、NEAT1等基因表达量较高,且SPP1通路间的细胞相互作用可能为阿尔茨海默病的潜在发病机制。 展开更多
关键词 单细胞转录组测序 阿尔茨海默病 数据图谱 拟时序分析 细胞通讯
暂未订购
基于共线性长测序数据的单染色体组装方法
16
作者 李梦然 甘祥超 《南京农业大学学报》 北大核心 2025年第4期969-976,共8页
[目的]本文提出一种基于长测序数据的单染色体组装方法,旨在更加准确高效组装出完整的基因组。[方法]利用GALA中的染色体分离算法,将初步组装中的contigs按染色体进行聚类,然后提取测序数据中的reads进行单染色体组装。受到测序数据质... [目的]本文提出一种基于长测序数据的单染色体组装方法,旨在更加准确高效组装出完整的基因组。[方法]利用GALA中的染色体分离算法,将初步组装中的contigs按染色体进行聚类,然后提取测序数据中的reads进行单染色体组装。受到测序数据质量和预组装结果的影响,有时contigs的聚类结果不够完美,导致后续单染色体组装难度增加。为了克服这一问题,提出了一种基于共线性分析辅助聚类的方法。该方法利用同物种或亲缘关系较近物种的参考基因组与GALA聚类生成的scaffolding groups进行共线性分析,根据比对结果将属于同一条染色体的scaffolding groups进行合并,使scaffolding groups中的序列长度与整条染色体相当,再根据合并后的结果提取reads进行单染色体组装。[结果]这套方法被应用在水稻(Oryza sativa)和桃金娘(Rhodomyrtus tomentosa)基因组组装,利用ONT的水稻测序数据组装出了长度379.89 Mb,N50为30.54 Mb,包含12条完整端粒到端粒的染色体。基于HiFi测序数据组装出总长度485.54 Mb,包含11条染色体,N50为46.71 Mb,不存在任何gap的桃金娘基因组。[结论]本文提出的组装方法不仅组装出准确完整的基因组,而且对不同种类的测序数据具有很强的适用性,为后续开展基因组学相关研究提供了可靠数据资源。 展开更多
关键词 基因组组装 长测序数据 单染色体组装 无间隙 共线性分析
在线阅读 下载PDF
食品微生物宏基因组测序数据分析方法的优化
17
作者 曾文苑 《现代食品》 2025年第20期163-165,共3页
食品当中的细菌、真菌、病毒等微生物将大幅增加食品安全风险,对广大人民群众的身体健康构成直接威胁。而在高通量测序技术飞速发展的今天,宏基因组测序数据分析在食品微生物溯源领域得到广泛应用,这种分析方法通过对食品微生物群落的... 食品当中的细菌、真菌、病毒等微生物将大幅增加食品安全风险,对广大人民群众的身体健康构成直接威胁。而在高通量测序技术飞速发展的今天,宏基因组测序数据分析在食品微生物溯源领域得到广泛应用,这种分析方法通过对食品微生物群落的基因组的全面深度分析,可以准确地获得微生物群落的组成、功能及潜在代谢途径,这就为保障食品安全、优化食品加工工艺、开发新型食品提供了有力的科学依据。基于此,本文围绕食品微生物宏基因组测序数据分析方法的优化策略展开论述,并强调指出宏基因组测序数据分析方法的应用前景与潜在价值,以期为食品微生物检测领域提供理论参考。 展开更多
关键词 食品微生物 宏基因组测序 数据分析 优化策略
在线阅读 下载PDF
Signac.UIO:基于R-Shiny技术的单细胞ATAC-seq数据交互式分析平台构建与应用
18
作者 罗玉燕 罗晓敏 +1 位作者 黄洁茹 徐斯文 《中国生物化学与分子生物学报》 北大核心 2025年第11期1579-1589,共11页
单细胞染色质可及性测序(Single-cell assay for transposase-accessible chromatin sequencing,scATAC-seq)是解析细胞异质性与基因调控网络的重要技术,在表观遗传研究中应用广泛。但其数据分析流程复杂和编程门槛高,阻碍了在非程序员... 单细胞染色质可及性测序(Single-cell assay for transposase-accessible chromatin sequencing,scATAC-seq)是解析细胞异质性与基因调控网络的重要技术,在表观遗传研究中应用广泛。但其数据分析流程复杂和编程门槛高,阻碍了在非程序员科研群体中的推广应用。为此,本文基于R语言的Shiny框架,整合Signac与Seurat等主流分析工具,开发了模块化、可视化的scATAC-seq数据分析平台--Signac.UIO。平台包含数据质控、细胞过滤、降维聚类、差异分析、细胞注释、通路富集、模体识别与转录因子足迹等10个功能模块,覆盖分析流程各关键环节。用户可通过图形界面完成操作,获得交互式可视化结果。平台已在PBMC公开数据集上验证其稳定性与实用性,现部署于服务器(https://xulabgdpu.org.cn/Signac.UIO),为单细胞表观组学研究提供了高效和易用的技术支撑。 展开更多
关键词 单细胞染色质可及性 R语言可视化平台 交互式分析平台 数据可视化 生物信息学工具
原文传递
基于数据挖掘技术的供电量精准预测系统设计研究
19
作者 时光宇 《粘接》 2025年第11期276-279,共4页
为实现城市电网供电量精准预测,提出搭建一个基于大数据的供电量分析与预测系统;首先,深入挖掘电网负荷历史数据中的有用信息;然后基于电网负荷序列分析结果构建一个双向预测模型,通过该模型实现历史数据有效处理,由此获得供电目标的月... 为实现城市电网供电量精准预测,提出搭建一个基于大数据的供电量分析与预测系统;首先,深入挖掘电网负荷历史数据中的有用信息;然后基于电网负荷序列分析结果构建一个双向预测模型,通过该模型实现历史数据有效处理,由此获得供电目标的月度用电量预测值;最后将该模型应用到搭建的系统中进行测试分析。实验结果表明,构建的模型可实现目标区域的供电量准确预测,其预测精度明显高于现有的线性回归、指数平滑预测方法,本方法对2024年不同月份的供电量预测结果更接近于真实值。说明采用本方法可实现城市电网供电量数据准确分析和预测,满足实际应用需求,具备可靠性和有效性。 展开更多
关键词 城市电网 数据挖掘 供电量 序列分析 双向预测
在线阅读 下载PDF
多表查询转换算法下的多平台共享数据一致性检验
20
作者 薛婷婷 王静武 +2 位作者 戴欣彤 张静 呼鑫 《移动信息》 2025年第11期102-104,120,共4页
多平台共享数据处理主要依托于模糊集合理论完成数据一致性检验,其在定义模糊规则时具有一定的主观性,导致检验结果的F1值较低。因此,文中提出了一种基于多表查询转换算法的新型多平台共享数据一致性检验方法。依托于多表查询转换算法... 多平台共享数据处理主要依托于模糊集合理论完成数据一致性检验,其在定义模糊规则时具有一定的主观性,导致检验结果的F1值较低。因此,文中提出了一种基于多表查询转换算法的新型多平台共享数据一致性检验方法。依托于多表查询转换算法对每个平台的共享数据分别进行查询,获取数据格式统一的数据时间序列。借助可变滑动窗口算法,分割完整的数据时间序列,形成多个等长数据序列。通过灰色关联度计算,评估两个等长数据序列之间的形状相似程度、距离接近程度,最终得出全面且客观的一致性检验结果。实验结果表明,运用所提方法得出的检验结果的F1值超过了0.9,实现了对数据一致性的准确描述。 展开更多
关键词 多表查询转换算法 多平台共享数据 一致性检验 滑动窗口 灰色关联分析 数据序列
在线阅读 下载PDF
上一页 1 2 11 下一页 到第
使用帮助 返回顶部