Searching journal content for articles similar to Bilgin Sonay et al. 25 (11): 1591.

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  1. .... The availability of two fully resolved haplotype assemblies from each ape species allowed for investigations into patterns of allelic variation and between-species comparisons of subterminal organization and differences in methylation patterns. We examined the telomeric transition regions from heterochromatin...
  2. ...Nijmegen, The Netherlands; 5Alzheimer Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam UMC location VUmc, 1081HV Amsterdam, The Netherlands Corresponding author: h.holstege@amsterdamumc.nlAbstractTandem repeats (TRs) occupy a significant portion of the human and are a source...
  3. ...contigs, except for contigs 16 and 17, which show enrichment only at one end (Supplemental Fig. S2). These two contigs carry 45S rDNA loci at the ends lacking telomeric repeats (see Results section “45S rDNA genes are organized as a single tandem array with only one diverging locus dispersed throughout...
  4. ...examples like histone genes (Maxson et al. 1983), rDNA arrays (Hall et al. 2022), and immunoglobulin genes (Watson and Breden 2012). Tandem repeats are prone to rapid copy number changes mediated through mechanisms such as unequal crossing over, replication slippage, gene conversion, and intrachromatid...
  5. ...to leverage high-quality protein sequences from closely related species. The output revealed a total of 11,545 protein-coding genes identified across both haplotypes, with 5737 genes in haplotype-a and 5808 genes in haplotype-b (Table 1; Fig. 2; Supplemental Data Set S3). The variation in gene count between...
  6. ...@usc.eduAbstractUnderstanding the impact of DNA variation on human traits is a fundamental question in human genetics. Variable number tandem repeats (VNTRs) make up ∼3% of the human but are often excluded from association analysis owing to poor read mappability or divergent repeat content. Although methods exist to estimate VNTR length...
  7. ...of transposable elements (TEs). For example, 46% of the human consists of TEs (Hoyt et al. 2022). In maize, in which TEs were first discovered, the is 85% TE sequences, of which 75% are long terminal repeat (LTR) retrotransposons (Schnable et al. 2009). In many species, TEs are intertwined with genes and...
  8. ...thaliana, a significant loss of ribosomal RNA (rRNA) genes with a past history of a mutation for the chromatin assembly factor 1 (CAF1) complex causes rapid changes in the structure. Using long-read sequencing and microscopic approaches, we have identified up to 15 independent large tandem duplications...
  9. ...observed two MITEs similar to one of the insertions in the proximal breakpoint, in agreement with the findings by Sharakhov et al. (2006) (Fig. 4). We also observed similar TE content in the 2Rb breakpoints as the one described by Lobo et al. (2010): tandem repeats flanking the inversion in the standard...
  10. ...controlling cell-extracellular matrix interactions, these tandem repeat variations tune human gene expression (Gymrek et al. 2016; Quilez et al. 2016), control nucleosome positioning (Volle and Delaney 2012), regulate circadian clocks (Sawyer et al. 1997), affect organismal morphology (Fondon and Garner 2004...
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