Searching journal content for articles similar to Alföldi and Lindblad-Toh 23 (7): 1063.

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  1. ...bp (De Coster et al. 2019; Mahmoud et al. 2019). Nevertheless, SRS remains the workhorse of genomics, producing many of the whole- and whole-exome data sets to study rare and complex diseases. Although SRS can readily identify single-nucleotide variants (SNVs) associated with disease, it often fails...
  2. ...kinetochore attachment sites pivotal for understanding karyotype diversity and evolution (Logsdon et al. 2024; Mastrorosa et al. 2024), as well as the notoriously repetitive ribosomal DNA (rDNA) arrays whose sequences have only been recently completed in humans (Nurk et al. 2022) and Arabidopsis (Fultz et al...
  3. ...the reference, such as disease- and trait-associated variants or engineered sequences. Recent work has applied synthetic regulatory genomics to characterized dozens of deletions, inversions, and rearrangements of DNase I hypersensitive sites (DHSs). Here, we use the state-of-the-art model Enformer to predict...
  4. ...2 functional genomics approaches to identify highly conserved endodermal cis-regulatory 30 modules (CRMs) functioning across the 400 million years of evolution separating zebrafish 31 and humans. Our analyses suggest that there are few endoderm-specific CRMs, with many 32 CRMs governing pancreas...
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  5. ...independently. If these similar traits are underlain by the same genetic changes, the genetic basis of adaptation might be predictable. Recent genomic studies, combined with smaller-scale genetic studies, have significantly advanced our understanding of this question (e.g., Brown et al. 2019; Sackton et al...
  6. ...6BT, United Kingdom; 2Cancer Evolution and Genome Instability Laboratory, The Francis Crick Institute, London NW1 1AT, United Kingdom; 3Cancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London WC1E 6DD, United Kingdom; 4University College London Cancer...
  7. ...-molecule profiling enabled by long-read sequencing (LRS) technologies. We highlight how LRS is transforming clinical and translational research, particularly by its ability to simultaneously measure genetic and epigenetic information, providing a more comprehensive understanding of complex disease mechanisms. We...
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  8. ...by highlighting its transformative potential and key hurdles, and emphasizing future opportunities for advancing the understanding of human genetic diversity and diseases through population-scale long-read analysis.The promise of long genomic reads for human population-scale studiesThe advent of long...
  9. ...56 changes during aging could yield essential insights into the disease’s pathophysiology. 57 Recent advances in single-cell genomics offer new opportunities to unravel the cellular 58 processes that link aging and PD pathology. Single-cell multiome sequencing(Vandereyken et al. 59 2023...
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  10. ...to be inconsistent with the relatively low rates of change in gene expression levels. This discrepancy has prompted the proposal of compensatory evolution as a prevalent mechanism for CREs (Schmidt et al. 2010; Berthelot et al. 2018). The phenomenon of CREs at nonorthologous genomic positions in different species...
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