Searching journal content for articles similar to Pezer et al. 25 (8): 1114.

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  1. Resource: Full-length RNA transcript sequencing traces brain isoform diversity in house mouse natural populations
    • Wenyu Zhang,
    • Anja Guenther,
    • Yuanxiao Gao,
    • Kristian Ullrich,
    • Bruno Huettel,
    • Aftab Ahmad,
    • Lei Duan,
    • Kaizong Wei,
    • and Diethard Tautz
    Genome Res. November 2024 34: 2118-2132; Published in Advance September 17, 2024, doi:10.1101/gr.279166.124
    ...(Guénet and Bonhomme 2003; Phifer-Rixey and Nachman 2015), the house mouse (Mus musculus) is a particularly suitable model system for studying the dynamics of polymorphisms and recently originated genetic elements in natural populations. Currently, three major lineages of the house mouse, which diverged...
  2. Method: Detecting differential copy number variation between groups of samples
    • Craig B. Lowe,
    • Nicelio Sanchez-Luege,
    • Timothy R. Howes,
    • Shannon D. Brady,
    • Rhea R. Daugherty,
    • Felicity C. Jones,
    • Michael A. Bell,
    • and David M. Kingsley
    Genome Res. February 2018 28: 256-265; Published in Advance December 11, 2017, doi:10.1101/gr.206938.116
    ...can identify a single location of copy number variation that correlates with ecotype instead of geography, whereas the substitution method only has statistical power when blocks of SNPs travel as a unit in marine and freshwater populations. These blocks of continuous marine/freshwater divergence may...
  3. Research: The rate and spectrum of new mutations in mice inferred by long-read sequencing
    • Eugenio López-Cortegano,
    • Jobran Chebib,
    • Anika Jonas,
    • Anastasia Vock,
    • Sven Künzel,
    • Peter D. Keightley,
    • and Diethard Tautz
    Genome Res. January 2025 35: 43-54; Published in Advance December 2, 2024, doi:10.1101/gr.279982.124
    .... Here, we provide the first estimates of the de novo mutation rate in the house mouse (Mus musculus) obtained from long-read sequencing of individuals from MA lines. To avoid reference bias and minimize false-positive variant calls, we built strain-specific chromosome-level assemblies from the MA line...
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