Searching journal content for articles similar to Decker et al. 25 (11): 1646.

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  1. ...-mer-spectra analysis revealed a similar size across all four sequenced individuals (mean size across k-mer sizes 20, 30, and 40: 800–817 Mb) and pointed toward lower estimates of -wide heterozygosity in both offspring (mean heterozygosity across k-mer sizes 20, 30, and 40; wildI: 0.097%, parent: 0.119%, offspring1: 0...
  2. ..., but not by the intersection calls, as false negatives; any calls reported by the intersection calls, but not by the consensus, as false positives. We calculated precision, recall, and F1 score to evaluate the accuracy of a call set against a truth set. Definitions of VAF bins, sequencing depth bins, clonality, and variant...
  3. ...with annotations of accessible chromatin regions identified using ATAC-seq data from the liver and brain. Analysis of the overlap between TEs and accessible chromatin revealed a large depletion of TEs in accessible chromatin. Although TEs represent ∼52% of the sequence, TE insertions only represent <20...
  4. ...metrics for constraint are available in the dog: constrained CDS, human ortholog LOEUF (loss of function observed over expected upper fraction), and variant phyloP score. Constrained CDS and variant phyloP score both represent evolutionary conservation of canine genomic sequence derived from the Zoonomia...
  5. ...offers guidance to design cost-effective experimental strategies that do not compromise on discovering novel biology.Over the last five years, long-read sequencing (LRS) technologies have transformed the landscape of genetic variant discovery in two fundamental ways. First, they have increased...
  6. ...at the Institute of Agriculture Biology and Biotechnology (IABB; CNR) (Morello et al. 2024). We performed 88× coverage short-read Illumina sequencing to account for potential genetic differences owing to independent clonal propagation over thousands of generations between this accession and that of the Rutgers...
  7. ...by DNA sequencing (ChIP-seq) of an ever growing number of TFs in different cell types, species, and conditions are revealing repeat-associated binding sites (RABS) whereby reproducible TF-DNA interactions fall within subtypes of major repeat families (Bourque et al. 2008). Coincident with their discovery...
  8. ...be used to identify crossovers from family sequencing data.As whole- sequencing (WGS) becomes ubiquitous, large family-based cohorts are now available, which have the potential to reveal more about how genetic material is transmitted within families and about how shared genetic material contributes...
  9. ...several duplicated chromosomes, contradicting current paradigms that asymmetrical evolution is specific to allopolyploids. Altogether, our results offer novel insights into evolutionary dynamics following ancient polyploidizations in vertebrates.Since the first teleost fish sequence was published in 2002...
  10. ...capture enrichment to obtain 100,000 -wide SNPs. The position of these SNPs was defined based on the coordinates available on the Canine HD BeadChip, ensuring its compatibility (full details about the methodology, such as bait design, capture experiment, sequencing, processing of raw reads, and genotyping...
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