Showing 921 - 940 results of 8,512 for search 'sequence evaluation', query time: 0.17s Refine Results
  1. 921
  2. 922

    Potential protective role of Bifidobacteria in myopia prevention: evidence from full-length 16S rRNA sequencing and bidirectional Mendelian randomization analysis by Guodong Tang, Yibo Han, Xiaoqi Gong, Xuejing Wang, Jing Li, Jun Zhang, Junru Wang, Jike Song, Jike Song, Hongsheng Bi, Hongsheng Bi

    Published 2025-08-01
    “…Subsequently, MR estimates were calculated using the inverse variance weighted, MR-Egger regression, and weighted median approaches, along with supplementary sensitivity evaluations. Concurrently, FDM was experimentally induced in guinea pigs, and fecal samples were subjected to comprehensive full-length 16S rRNA gene sequencing analysis.ResultsMR analysis identified five bacterial taxa linked to the risk of myopia. …”
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  3. 923
  4. 924

    Transcriptome sequencing revealed that lymph node metastasis of papillary thyroid microcarcinoma is associated with high THBS4 expression and PDGFRA+ cancer-associated fibroblasts by LeYin Hu, Yi Lin, JingYu Zheng, Li Wan, Rui Zhao, Yi Ma, JianMin Li

    Published 2025-04-01
    “…The study defined two groups of PTMC patients: LNM(n=50) and NLNM(n=50). 10 samples from each group were used for transcriptome sequencing. The expression of THBS4 was evaluated in both groups. …”
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  5. 925

    Next-generation diagnostics of bloodstream infections enabled by rapid whole-genome sequencing of bacterial cells purified from blood culturesResearch in context by Vincenzo Di Pilato, Chiara Bonaiuto, Fabio Morecchiato, Alberto Antonelli, Tommaso Giani, Gian Maria Rossolini

    Published 2025-04-01
    “…We developed a analytical workflow named LC-WGS (Whole-Genome Sequencing of Liquid Colony) for rapid whole-genome sequencing-based diagnosis of BSI, evaluating its accuracy performance over standard of care (SoC) diagnostic procedures. …”
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  6. 926

    Sequence and protein three-dimensional structure analysis of a novel inter-allelic recombination allele B*35∶186 of HLA-B locus by ZHANG Xu, LIN Fengqiu, LI Xiaofeng, LI Jianping

    Published 2025-03-01
    “…Sequence-based typing (SBT) and gene clone were used to analyze exons 1-4 sequences of HLA-B allele. …”
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    Article
  7. 927

    ANALYSIS OF DIFFERENTIAL ExPRESSION OF MATRIx METALLOPROTEASES IN STABLE AND UNSTABLE ATHEROSCLEROTIC LESIONS BY A METHOD OF FULL GENOME SEQUENCING OF RNA: PILOT STUDY by D. Е. Ivanoschuk, Yu. I. Ragino, E. V. Shakhtshneider, S. V. Mikhailova, V. S. Fishman, Ya. V. Polonskaya, E. V. Kashtanova, A. M. Chernyavsky, I. S. Murashov, М. I. Voevoda

    Published 2018-09-01
    “…To analyze differential expression of metalloproteases genes, involved into the processes of stabilization/destabilization of atherosclerotic plaque, with the method of full genome sequencing of RNA, and to evaluate the level of metalloproteases in homogenates of plaques of various types by immune enzyme assay method (IEA).Material  and  methods.  …”
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  8. 928

    Dynamic relationship between gut microbiota and post-necrotizing pancreatitis: insights from a multi-stage 16S rRNA sequencing study by Jiongdi Lu, Jiongdi Lu, Zhe Wang, Zhe Wang, Feng Cao, Feng Cao, Jia Li, Guofeng Ji, Guofeng Ji, Fei Li, Fei Li

    Published 2025-05-01
    “…Clinical data were correlated with GM profiles to evaluate associations.Results29.5% and 19.1% of NP patients progressed to pancreatic endocrine and exocrine insufficiency, respectively. …”
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    Article
  9. 929

    Phosphate transporter gene families in rye (Secale cereale L.) – genome-wide identification, characterization and sequence diversity assessment via DArTreseq by David Chan-Rodriguez, Brian Wakimwayi Koboyi, Sirine Werghi, Bradley J. Till, Julia Maksymiuk, Fatemeh Shoormij, Abuya Hilderlith, Anna Hawliczek, Maksymilian Królik, Hanna Bolibok-Brągoszewska

    Published 2025-06-01
    “…The aim of this study was to: (i) identify and characterize putative members of different phosphate transporter families in rye, (ii) assess their sequence diversity in a collection of 94 diverse rye accessions via low-coverage resequencing (DArTreseq), and (iii) evaluate the expression of putative rye Pht genes under phosphate-deficient conditions. …”
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  10. 930
  11. 931

    Comparison of pathogen detection performance between metagenomic next-generation sequencing and conventional culture in organ preservation fluids and recipient wound drainage fluid... by Jiyuan Li, Wenjia Yuan, Chen Gao, Lei Liu, Lei Song, Wei Cao, Xuejing Zhu, Yachun Han, Ruobing Liang, Gongbin Lan, Shaojie Yu, Yu Wang, Liang Tan, Helong Dai, Xubiao Xie, Longkai Peng, Fenghua Peng

    Published 2025-08-01
    “…This study aims to assess the effectiveness of metagenomic next-generation sequencing (mNGS) in detecting pathogens within donor organ preservation fluids and recipient wound drainage fluids, with a comparison made against conventional culture methods.MethodsThis study involved 141 kidney transplant patients (May 1st, 2020 to Jan 31st, 2024). …”
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  12. 932

    Highly multiplexed molecular inversion probe panel in Plasmodium falciparum targeting common SNPs approximates whole-genome sequencing assessments for selection and relatedness by Karamoko Niaré, Karamoko Niaré, Rebecca Crudale, Abebe A. Fola, Abebe A. Fola, Neeva Wernsman Young, Victor Asua, Victor Asua, Melissa D. Conrad, Pierre Gashema, Anita Ghansah, Stan Hangi, Deus S. Ishengoma, Deus S. Ishengoma, Jean-Baptiste Mazarati, Ayalew Jejaw Zeleke, Philip J. Rosenthal, Abdoulaye A. Djimdé, Abdoulaye A. Djimdé, Jonathan J. Juliano, Jonathan J. Juliano, Jonathan J. Juliano, Jeffrey A. Bailey, Jeffrey A. Bailey

    Published 2025-06-01
    “…We optimized the panel alone and in combination with antimalarial drug resistance MIPs in laboratory P. falciparum strains at different parasitemias and validated it by sequencing field isolates from the Democratic Republic of Congo, Ethiopia, Ghana, Mali, Rwanda, Tanzania, and Uganda and evaluating the population structure, identity-by-descent (IBD), signals of selection, and complexity of infection (COI).ResultsThe new panel IBC2FULL consisted of 2,128 MIPs (containing 4,264 common SNPs) spaced by 5.1–18.4 kb across the entire genome. …”
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  13. 933

    Optimisation and clinical validation of a metagenomic third-generation sequencing approach for aetiological diagnosis in bronchoalveolar lavage fluid of patients with pneumoniaRese... by Shanshan Zhang, Xi Li, Xia Li, Ying Fu, Long Chen, Wei Wang, Qinqing Lin, Hui Lou, Yake Yao, Wenyu Chen, Cheng Zhong, Jian Ye, Yinan Yao, Huimin Guo, Yunsong Yu, Hua Zhou

    Published 2025-06-01
    “…Summary: Background: Metagenomic Third Generation Sequencing (mTGS), based on nanopore technology, has emerged as a promising tool for the rapid diagnosis of pneumonia pathogens. …”
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    Article
  14. 934

    Genetic Diversity of Peach (<i>Prunus persica</i>) Accessions Collected in Northern Vietnam Using ISSR Markers by Dinh Ha Tran, Thanh Huyen Dao, Xuan Binh Ngo, Van Hong Nguyen, Thanh Van Dao, Tien Dung Nguyen

    Published 2025-02-01
    “…This study investigated the genetic diversity of 59 peach accessions collected from northern mountainous provinces in Vietnam using ISSR (inter-simple sequence repeat) markers. The obtained results enabled the evaluation of genetic variation and relationships among peach varieties, which supports breeding programs and germplasm conservation. …”
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  15. 935

    A Spatial Decision Support Model for Fire Station Construction Prioritization Under Resource Constraints by Yuan Zeng, Dingli Liu, Diping Yuan, Weijun Liu, Guohua Wu, Xiao Lei

    Published 2025-06-01
    “…The construction urgency of the proposed fire stations was assessed using the construction sequence scoring equation. To validate the model, a case study of Shaoyang City, China, was conducted. …”
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  16. 936
  17. 937

    Rare urogenital malformation with prune belly syndrome in a newborn female: A case report by Melanie Elhafid, Kristopher Milbrandt

    Published 2025-04-01
    “…Urorectal septum malformation sequence (URSMS) is an even more rare congenital anomaly defined by the presence of ambiguous genitalia, absent perineal openings, and lumbosacral abnormalities. …”
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  20. 940

    A novel evaluation of genetic polymorphism in BCG adenitis by Maryam Hassanzad, Poupak Farnia, Sepideh Darougar, Ali Akbar Velayati

    Published 2019-06-01
    “…Then genotyping for known mutations was performed using restriction fragments length polymorphism (PCR-RFLP) assays. Sequencing was performed for IL-12 Rβ1, IFN-ϒ receptor 1, IL-10, TNF-α and P2X7. …”
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