Searching journal content for articles similar to Rasmussen and Kellis 17 (12): 1932.

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  1. ...to the proteotranscriptomics-validated ORFs, that is, those supported by peptide evidence. Thus, we used 1516 orthology protein groups that only have one-to-one orthologs across all species. By multiple alignment of these protein sequences, we reconstructed individual gene trees for each orthology group with three different...
  2. ...of the loci at the speciationnodeswould allowus to infer evolution within each species tree branch independently of one another. Therefore, rather than inferring the locus map and order for the entire gene tree at once, we consider the subproblem of determining species-specific locus maps and orders...
  3. ...and drifts until it fixes or goes extinct. Duplications, losses, and coalescence Genome Research 757 www..org that the blue tree in Figure 2A is not a species tree (e.g., species B and C are represented multiple times), and yet it is distinct from the gene tree. Therefore, it is a third kind of tree, which...
  4. ...et al. 2021).The evolution of complex insect societies represents one of the major evolutionary transitions (Maynard Smith and Szathmáry 1995). Genomic signatures of this transition share few commonalities across taxa, except for an increase in gene regulatory capacity (Gadau et al. 2012; Simola et...
  5. ...tandem duplications as the predominant drivers of gene expansion in these gene clades. The many short species-specific tandem arrays in the bottom half of A and C and throughout D indicate that genomic transpositions followed by tandem duplications drove expansions in these clades.To examine the genomic...
  6. ...to be most accurate for identifying functional counterparts ( Hulsen et al. 2006 ). Nonetheless, the transfer can be done in many ways in case of multiple co-orthologs (inparalogs) stemming from species-specific gene duplication, which is commonplace in eukaryotes. As shown in Figure 4 , the FC may evolve...
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