Searching journal content for articles similar to Schmitz et al. 23 (10): 1663.

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  1. ...(Janku et al. 1980; Parker and Landstrom 2021; Kingdom and Wright 2022). A potential explanation for these phenomena is oligogenic inheritance, or a type of inheritance in which a few variants are required in combination to cause a particular phenotype (Kousi and Katsanis 2015).Previous work has...
  2. ...discuss current challenges and future directions in the field, emphasizing the need for innovative computational tools and robust, reproducible approaches to fully harness the capabilities of LRS in molecular diagnostics.What is methylation?Cytosine DNA methylation (5mC) involves the covalent modification...
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  3. ...author: ryan.lister@uwa.edu.auAbstractIn plants, cytosine DNA methylation (mC) is largely associated with transcriptional repression of transposable elements, but it can also be found in the body of expressed genes, referred to as gene body methylation (gbM). gbM is correlated with ubiquitously expressed...
  4. ...and forthcoming449 genetic mapping data obtained from the BxD recombinant inbred strain panel. Samples were450 harvested from the mice at 12 weeks of age.451 Liver perfusion452 To purify hepatocytes from the liver cell population, the mouse livers were perfused with 87453 CDU/mL Liberase collagenase with 0.02% Ca...
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  5. ...-molecule sequencing technologies (Oxford Nanopore Technologies [ONT] and Pacific Biosciences [PacBio]) have enabled readouts of long, native DNA molecules, including cytosine methylation. ONT recently upgraded their Nanopore sequencing chemistry and kits from the R9 to the R10 version, which yielded increased...
  6. ...that arise from recent demographic events, patterns that are crucial for understanding rare variant effects. To address this challenge, we propose a novel method called spectral components (SPCs), which leverages identity-by-descent (IBD) graphs to capture and transform local, nonlinear fine-scale population...
  7. ...similar to those of HL. KEGG analysis showed that these genes were also enriched in pathways such as “DNA repair and recombination proteins” and “MAPK signaling pathway” (Supplemental Fig. 6C,D).More hypo-DMRs can be inherited by the next generationTo investigate whether variations in DNA methylation...
  8. ...traits, which at the molecular level often involves complex interactions between genetic variants, the epi, and gene expression. DNA methylation (DNAm) refers to the addition of methyl groups to cytosine bases, usually within CpG dinucleotide contexts (the most commonly methylated motif in mammals). DNAm...
  9. ...prioritized according to functional impact, we can identify trait associations for variants often overlooked by traditional -wide association studies (GWASs).The rigid population structure and extreme phenotypic diversity across breeds is an essential component of our analysis. By definition, dog breeds...
  10. ...) precludes the detection of deaminated cytosines in methylated CpG contexts (i.e., TCG and CCG). Moreover, the impact of chromatin organization on deamination rates was largely unexplored, possibly owing to high levels of background deamination during library preparation.Here, we develop a new method called...
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