Searching journal content for articles similar to Sholes et al. 32 (4): 616.

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  1. ....fischer@sorbonne-universite.fr, zhou.xu@sorbonne-universite.frAbstractTelomeres gradually shorten at each cell division, and telomerase counteracts this shortening by elongating telomere sequences. This dynamic balance between elongation and shortening results in a steady-state telomere length (TL) distribution. Here, we develop...
  2. ...-induced cell death, many managed to survive telomerase absence and must have therefore found a solution to maintain and protect telomeres. In this work, using long-read Oxford Nanopore Technologies (“Nanopore”) sequencing able to traverse large repeated regions, we investigated instability in telomerase...
  3. ...technologies, it is now possible to assemble through human centromeres (Nurk et al. 2022). More recent methods, including NTRprism (Altemose et al. 2022), HORmon (Kunyavskaya et al. 2022), and HiCAT (Gao et al. 2023), can identify detailed chromosome-specific HOR patterns from complete SatDNA sequences...
  4. ...Bio) SMRT technology and Oxford Nanopore Technologies have cast illumination on previously dark matter, allowing assembly of previously intractable arrays. Whereas short sequencing reads have defined the point centromeres of budding yeast (Fitzgerald-Hayes et al. 1982) and short regional centromeres...
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  5. ...of centromere tandem repeat arrays has been limited in many species, as they could not be fully assembled using short-read sequencing (Miga and Sullivan 2021). However, Oxford Nanopore Technology (ONT) and Pacific Biosciences (PacBio) HiFi long-read sequencing now allow complete assembly of complex centromere...
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  6. ...region begins with chromosome-specific sequences followed by a conserved ribosomal RNA cluster that is followed by the duplicated subtelomeric region and telomere. There are many ONT and PacBio reads that link the unique chromosomal regions and the beginning of the subtelomeric gene families but only...
  7. ...Nanopore Technologies (ONT) platform now can routinely generate sequencing reads in excess of 100 kbp (so-called ultralong [UL] sequencing reads) (Nurk et al. 2020; Shafin et al. 2020; Logsdon et al. 2021). The use of parent–child trio (trio-hifiasm) Illumina whole- sequencing (WGS) data in conjunction...
  8. .../86) overlap complete protein-coding sequence, and 15% (13/86) overlap one or more full-length D. melanogaster genes. In total, 32 complete coding sequences were duplicated, or 12.8 new genes per million years. Similar to the polymorphic duplicates in D. simulans (Rogers et al. 2014), tandem duplications fixed...
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