Searching journal content for articles similar to Siepel 19 (11): 1929.

Displaying results 1-10 of 44
For checked items
  1. ...; and deleted bases are gray. The inserted sequence was not found in GRCh38 but was present in nonhuman primates and likely represents the deletion of ancestral sequence where the reference contains the derived (deleted) allele.Many differences in the PGGB SVs are attributable to different breakpoint choices...
  2. ...et al. 2007; Thomson et al. 2010), AE loci (Lemmon et al. 2012), or UCE loci (Faircloth et al. 2012). In phylogenomic studies involving populations or species that diverged recently or rapidly, coalescent theory predicts that neutral genomic loci will often have retained ancestral polymorphisms...
  3. ...maximum-likelihood analysis with the phytools package (Revell 2012), applying the fastAnc function to reconstruct ancestral states according to divergence times and size. Additionally, we counted the active TE copies for each species and generated a heat map for comparison.Population structure...
  4. ...populations, because the individuals from these species in our study are from managed laboratory research colonies. Comparative RNA sequencing in endangered primates Genome Research 605 www..org protein might be explained by adaptive nucleotide substitutions that occurred in ancestral primate lineages...
  5. ...different preferences. Transposable elements are a source of genetic novelty between populations and species, driving rapid adaptive evolution. However, the extent of TEs’ contribution to host shift remains unexplored. Here, we perform genomic and transcriptomic analyses in six s of cactophilic species...
  6. ..., and Diptera, and the 800 Mb grasshopper X Chromosome is homologous to the fly ancestral X Chromosome despite 400 million years of divergence, suggesting either repeated origin of sex chromosomes with highly similar gene content, or long-term conservation of the X Chromosome. We use this broad conservation...
  7. ...2-way alignments. We designed the tool for easy use as an extremely powerful, web-interactive platform. Herein we show the power of 2-n-way with some prime examples spanning the scope of architecture, functional genomics, population genomics, and phylogenomics.ResultsFrom a well-characterized target...
  8. ...2007) and propelled population and phylogenomic inferences to successful applications that span several fields of biology and biomedicine (Siepel 2009; Rogers and Gibbs 2014). Coalescent-based models allow for estimating the values of parameters, including population divergence times, mutation...
  9. ...species without being reproductively isolated (McGaughran et al. 2016). The resulting combination of species and population-level phylogenomic data allows us to perform evolutionary comparisons at various timescales and to provide empirical support for the rapid turnover hypothesis...
  10. .... These authors further suggested that these three primate gene families share a common X-linked ancestor with the murine ampliconic Spanx and Cypt orthologous gene families.In contrast, the mouse X Chromosome possesses only 50% of the ancestral ampliconic CTA gene families (Table 3), having lost orthologs...
For checked items

Preprint Server