Searching journal content for articles similar to Arimizu et al. 29 (9): 1495.

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  1. ...analyses in cancer genomics.The ability of ScisTree2 to analyze a large number of cells may be useful in large-scale cancer genomics analyses. One such analysis is identifying rare cancer subclones, which can drive disease recurrence and therapy resistance. For example, relapse of acute myeloid leukemia...
  2. ...tools enables high-fidelity, large-scale profiling of microsatellites, which may find utility in diverse applications such as lineage tracing, population genetics, ecology, and forensics.Microsatellites, also known as short tandem repeats, are genomic sequences composed of tandem repeats of short (1...
  3. ...genes (SSOGs). SSOGs cannot be explained by the insufficient sequencing of homologous sequences, because each typically contains additional genes that cannot be found in other s, as, for example, observed in Escherichia coli (Yu and Stoltzfus 2012). Also, genes specific to E. coli have been found...
  4. ...this gene could provide a viable therapeutic target in dogs (Urick and Bell 2020; Kawaguchi et al. 2021; Urick et al. 2021).Sequencing strategies for large-scale genomic analysesIn the past 10 years, there has been a steady decrease in the cost of short-read whole- sequencing (WGS) (Cullen and Friedenberg...
  5. ...blood- or urine-derived isolates of extraintestinal pathogenic (ExPEC) Escherichia coli, a common agent of sepsis and community-acquired urinary tract infections, obtained during the course of routine clinical care at a single institution. We find that ExPEC E. coli are highly genomically heterogeneous...
  6. ...-Relate on the UK Biobank and All of Us data sets. On a data set of 200,000 individuals split between two parties, SF-Relate detects 97% of third-degree or closer relatives within 15 h of runtime. Our work enables secure identification of relatives across large-scale genomic data sets.Collaborative studies that aim...
  7. .... 2020. Benchmarking principal component analysis for large-scale single-cell RNA-sequencing. Genome Biol 21: 9. doi:10.1186/s13059-019-1900-3 ↵van der Maaten L, Hinton G. 2008. Visualizing data using t-SNE. J Mach Learn Res 9: 2579–2605. ↵van Dijk D, Sharma R, Nainys J, Yim K, Kathail P, Carr AJ...
  8. ...is accompanied by the formation of de novo enhancer contacts and activation of MYC, illustrating how structural genomic variants can alter the 3D during oncogenesis. In summary, our findings provide evidence for the loss of organization at multiple scales during breast cancer progression, revealing novel...
  9. ...Large-scale detection and characterization of interchromosomal rearrangements in normozoospermic bulls using massive genotype and phenotype data sets Jeanlin Jourdain,1,2 Harmonie Barasc,3 Thomas Faraut,3 Anne Calgaro,3 Nathalie Bonnet,3 Camille Marcuzzo,4 Amandine Suin,4 Anne Barbat,2 Chris Hozé,1...
  10. ...are emerging as a model system to understand the molecular evolution of living fossil lineages (Braasch et al. 2016; Thompson et al. 2021; Brownstein et al. 2022a, 2024; Simakov et al. 2022). To better understand rates of genomic evolution in gars, we estimated nucleotide substitution and structural change...
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