Searching journal content for articles similar to Li et al. 34 (12): 2304.

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  1. ...Científicas, 50059, Zaragoza, Spain; 2European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton CB10 1SD, United Kingdom; 3University of Liverpool, Institute of Systems, Molecular and Integrative Biology, Liverpool L69 7ZB, United Kingdom; 4Department of Botany...
  2. ...Quadrupia provides a comprehensive catalog of G-quadruplexes across s from the tree of life Nikol Chantzi1,11, Akshatha Nayak1,11, Fotis A. Baltoumas2,3,11, Eleni Aplakidou2,3, Shiau Wei Liew4,5, Jesslyn Elvaretta Galuh4,5, Michail Patsakis1, Austin Montgomery1, Camille Moeckel1, Ioannis Mouratidis...
  3. ...sequencing-based map of normal patterns of human genetic variation for filtering and prioritizing candidate disease-causing variants (International HapMap Consortium 2005; The 1000 Genomes Project Consortium 2015; Byrska-Bishop et al. 2022). The impact of 1KGP on our understanding of human genetic diversity...
  4. ...cellular folding properties, distinguishing them from nonhierarchical TADs. For instance, Llères et al. (2019) showed the involvement of hierarchical TADs in activating genomic imprinting during mouse development. Meanwhile, Hanssen et al. (2017) uncovered that hierarchical TAD boundaries, particularly...
  5. ...confidentiality and integrity of the computation. We introduce novel data-oblivious algorithmic techniques based on compressed reference panels and dynamic fixed-point arithmetic that comprehensively mitigate side-channel leakages in TEEs to provide robust protection of users’ genomic data throughout the analysis...
  6. ...). The common practice of benchmarking experimental assays on a single European ancestry limits our knowledge of how genetic variation impacts functional genomic mechanisms and perpetuates biases in genomic research (Gurdasani et al. 2019; Mills and Rahal 2020). To improve upon these shortcomings, we developed...
  7. ...; Meštrović et al. 1998). Modern sequencing technologies and accompanying bioinformatics tools have improved the detectability of satDNAs, disclosing often more than one hundred satDNAs in different organisms (Boštjančić et al. 2021; João Da Silva et al. 2023). Consequently, high-throughput satellitome...
  8. ...). We investigate the genomic organization of the MHC region, ontogenetic and tissue-specific expression profiles, and the evolutionary history of the MHC gene family. To achieve this, we integrated publicly available chromosome-scale assemblies from four newt species with newly generated long...
  9. ....1101/gr.279322.124 ↵Porter VL, Ng M, O'Neill K, MacLennan S, Corbett RD, Culibrk L, Hamadeh Z, Iden M, Schmidt R, Tsaih S-W, et al. 2025. Rearrangements of viral and human s at human papillomavirus integration events and their allele-specific impacts on cancer regulation. Genome Res (this issue) 35: 653...
  10. ...impact of NUMT integration, we identified mitochondrial insertions in the nuclear s of more than 1000 mammalian and avian species. Specifically, we analyzed 680 mammalian and 458 avian s with both nuclear and mitochondrial assemblies available from public databases. Using a previously published...
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