Searching journal content for articles similar to Nygaard et al. 21 (8): 1339.

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  1. ...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...
  2. ...recombination in honey bees, let alone in other social Hymenoptera. In ants, two studies conducted in Acromyrmex echinatior (Sirviö et al. 2006) and Pogonomyrmex rugosus (Sirviö et al. 2011b) using a limited number of markers (145–215 markers) corroborated elevated recombination rates in social insects. However...
  3. ...-resolved assemblies have become the norm in eukaryotic genomics with advances in long-read sequencing technologies. Complete assemblies are fundamental for addressing key questions in biology that were previously hidden in the “dark matter” of s. Key breakthroughs have revolved around centromeres and the embedded...
  4. ...contributed equally to this work. Corresponding authors: thomas.near@yale.edu, clad@ihb.ac.cn, yangliandong1987@163.comAbstractGenomic evolution can propel and restrict species diversification. Rapid molecular evolution and genomic rearrangement is often associated with increased species diversification...
  5. ...used for genomic DNA capture. This method facilitated the successful capture and sequencing of ADGRV1 transcripts as well as full-length 18.9 kb USH2A transcripts. By combining algorithmic analysis with detailed manual curation of sequenced reads, we identified novel isoforms characterized...
  6. ...developed by Pacific Biosciences (PacBio) and Oxford Nanopore Technologies (ONT), have revolutionized genomic and transcriptomic research. Their ability to generate very long reads has enabled significant advancements, including complete sequencing of human chromosomes (Nurk et al. 2022) and full...
  7. ...:10.1038/s41587-022-01652-0 ↵Gall-Duncan T, Sato N, Yuen RKC, Pearson CE. 2022. Advancing genomic technologies and clinical awareness accelerates discovery of disease-associated tandem repeat sequences. Genome Res 32: 1–27. doi:10.1101/gr.269530.120 ↵Genner R, Akeson S, Meredith M, Jerez PA, Malik L...
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  8. ...al. 2023), especially with the development of advanced tools (Li et al. 2017; Raeisi Dehkordi et al. 2021). OGM has been used to successfully identify constitutional genomic lesions, despite some limitations (Dremsek et al. 2021; Mantere et al. 2021; Sahajpal et al. 2021; Dai et al. 2022...
  9. ...: chirag@iisc.ac.inAbstractAffordable genotyping methods are essential in genomics. Commonly used genotyping methods primarily support single-nucleotide variants and short indels but neglect structural variants. Additionally, accuracy of read alignments to a reference is unreliable in highly polymorphic...
  10. ...the N2-derived strain VC2010. Moreover, genetically divergent versions of N2 have arisen over decades of research and hindered reproducibility of C. elegans genetics and genomics. Here we provide a 106.4 Mb gap-free, telomere-to-telomere assembly of C. elegans, generated from CGC1, an isogenic...
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