Searching journal content for articles similar to Liddiard et al. 26 (5): 588.

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  1. ...(Ma and Nt, 506 and 347 complete phenotypes, respectively) showed highly significant differences for all traits studied. In six of the eight bulls studied, we found that balanced daughters had significantly delayed first inseminations compared with their wild-type sisters, thus supporting growth...
  2. ...requires the presence of a homologous sequence of DNA (most commonly a sister chromatid) to serve as a template that can be used to resynthesize DNA sequences. However, except in special circumstances such as MAT switching, where the donor is heterochromatic with highly positioned nucleosomes...
  3. ...and Cooper 2010; Wellinger and Zakian 2012; de Lange 2018). These functions are tightly associated with the regulation of telomere length (TL). Indeed, telomeres are protected by proteins that prevent natural chromosome ends from being recognized as double-strand breaks, which would elicit a DNA damage...
  4. ..., respectively; the rDNA repeats, in light green; the distal satellite regions, in orange; and the telomeres, in dark green. Each distal satellite is labeled according to the HG002 v1.0.1 reference assembly, with the exception of Chromosome 13 and Chromosome 22 paternal, which are too similar to be separated...
  5. ...Cell-type- and chromosome-specific chromatin landscapes and DNA replication programs of Drosophila testis tumor stem cell–like cells Jennifer A. Urban1, Daniel Ringwalt1, John M. Urban2,3, Wingel Xue1,5, Ryan Gleason1, Keji Zhao4 and Xin Chen1,2 1Department of Biology, The Johns Hopkins University...
  6. ...Toward telomere-to-telomere cat s for precision medicine and conservation biology William J. Murphy1,2,3 and Andrew J. Harris1,3 1Department of Veterinary Integrative Biosciences, Texas A&M University, College Station, Texas 77843-4458, USA; 2Department of Biology, Texas A&M University, College...
  7. ...different sequencing depths. Here, we used equal sequencing depths on both haplotypes. (C,D) Fraction of sequencing outputs containing an assembly gap when the sequencing depths across the two haplotypes are uneven. This scenario models somatic mutation in DNA with variant allele frequency below 0.5. In (C...
  8. ...polymerase IV, which lacks strand displacement and exonuclease activity, was used to generate a double-stranded blunt end, as well as T4 DNA ligase to seal the nicks. Nanopore library adaptors were added to allow sequencing (Fig. 1A).View larger version: In this window In a new window Figure 1. Telomere...
  9. ...for feature encoding schemes was further analyzed across 11 species. We encoded all the 11 data sets from EpiTEAmDNA by 14 feature encoding schemes and evaluated ACC via three DL base models on independent test sets, thus quantifying feature selectivity across species and models to uncover encoding...
  10. ...of peaks. (B) The density of ChIP-seq peak positions along the Arabidopsis chromosomes, relative to their distance from the centromere (C, on the left) to the telomere of the chromosome arm they are on (T, on the right). (C) Average DNA methylation levels in WT Arabidopsis seedlings under protein...
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