Showing 2,881 - 2,900 results of 5,161 for search '"genomics"', query time: 0.06s Refine Results
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    Modeling compositional heterogeneity resolves deep phylogeny of flowering plants by Yongli Wang, Yan-Da Li, Shuo Wang, Erik Tihelka, Michael S. Engel, Chenyang Cai

    Published 2025-01-01
    “…Here we show that, although plastid and mitochondrial genomes lack sufficient phylogenetic signal for resolving deeper phylogeny, the relationships among five mesangiosperm lineages can be confidently resolved under better-fitting models using genome-scale data. …”
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    Unravelling single-cell DNA replication timing dynamics using machine learning reveals heterogeneity in cancer progression by Joseph M. Josephides, Chun-Long Chen

    Published 2025-02-01
    “…Abstract Genomic heterogeneity has largely been overlooked in single-cell replication timing (scRT) studies. …”
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  5. 2885
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    Phylogenomic analysis reveals exceptions to the co-evolution of ZAR1 and ZRK immune gene families in plants by Li Yang, Shengyi Liu, M. Eric Schranz, Klaas Bouwmeester

    Published 2025-01-01
    “…All analysed monocot genomes thus far examined, except for the aroid Colocasia esculenta, were previously reported to lack both ZAR1-A and ZRKs. …”
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    ANIONIC PEROXIDASE GENE POLYMORPHISM IN WHEAT by I. V. Maksimov, G. F. Burkhanova, O. I. Kuzmina, V. A. Vakhitov

    Published 2018-06-01
    “…., T. urartu Thum. ex Gandiljan and T. aestivum (media genomes Au) clustered to the subgenus Triticum. Species T. compactum, T. durum, T. macha, T. spelta, T. turgidum, T. urartu and T. aestivum (media genomes Ab) clustered together to the subgenus Boeoticum Migusch. et Dorof. …”
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  13. 2893

    Schistosoma Tegument Proteins in Vaccine and Diagnosis Development: An Update by Cristina Toscano Fonseca, Gardênia Braz Figueiredo Carvalho, Clarice Carvalho Alves, Tatiane Teixeira de Melo

    Published 2012-01-01
    “…Bioinformatics tools, together with the access to parasite genome, published recently, should help generate new knowledge on parasite biology and search for new vaccines or therapeutic targets and antigens to be used in the disease diagnosis. …”
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  14. 2894

    Gene Array Studies in Renal Neoplasia by John P.T. Higgins

    Published 2006-01-01
    “…For these reasons, renal cell carcinoma is ideally suited to the genome scale investigation made possible by DNA microarrays. …”
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  15. 2895

    Prenatal Diagnosis of Cystic Hygroma related to a Deletion of 16q24.1 with Haploinsufficiency of FOXF1 and FOXC2 Genes by Matthew J. Garabedian, Donna Wallerstein, Nubia Medina, James Byrne, Robert J. Wallerstein

    Published 2012-01-01
    “…This case highlights the power of whole genomic aCGH to further delineate the etiology of birth defects.…”
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  16. 2896

    RNA splicing: a split consensus reveals two major 5′ splice site classes by Matthew T. Parker, Sebastian M. Fica, Gordon G. Simpson

    Published 2025-01-01
    “…The two 5′ splice site classes are separable in genome sequences, sensitized by specific genotypes and associated with splicing complexity. …”
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  17. 2897

    Different Genotypes of the Rare and Threatened Moss <i>Physcomitrium eurystomum</i> (Funariaceae) Exhibit Different Resilience to Zinc and Copper Stress by Djordje P. Božović, Marija V. Ćosić, Vladislav Kolarčik, Michal Goga, Claudio Varotto, Mingai Li, Aneta D. Sabovljević, Marko S. Sabovljević

    Published 2025-01-01
    “…Flow cytometry analyses revealed that the two accessions differ significantly in terms of genome size. However, the different amplitude of resilience to the tested PTEs, the divergence in physiological responses, and survival within two accessions of the same species are confirmed, as well as the dissimilarity of their genome size, likely associated with ploidy level difference and possibly distinct hybrid origin.…”
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    Trajectory of human migration: insights from autosomal and non-autosomal variant clustering patterns by Samayeta Sarkar Tuli, Joyatry Sarker, Mrinmoy Saha Roddur, Anik Biswas, Reefa Nawar, Tahmina Akter, Md. Wahid Murad, Abu Ashfaqur Sajib

    Published 2025-03-01
    “…Moreover, the genetic markers on the Y chromosome constitute only a minor fraction of the entire human genome. Here, we analyzed over 75 million genetic variants (single nucleotide variants (SNVs) and short insertion-deletion (InDels)) within consecutive 2500000 base pair windows in the autosomal as well as non-autosomal chromosomes of 22 populations in four major geographic regions that are cataloged in the 1000 Genomes Project to understand the clustering patterns of the autosomal and non-autosomal variants. …”
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