Searching journal content for articles similar to Bashir et al. 15 (7): 998.

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  1. .... In exemplar yeast and mammalian data sets, we demonstrate that the predictive power of ERC2.0 is improved relative to the previous method, ERC1.0, and that further improvements are obtained by using larger yeast and mammalian phylogenies. We attribute the improvements to both the larger data sets and improved...
  2. ...mammalian species to detect significant correlations between the relative evolutionary rates of genes and changes in diet. We have identified six genes—ACADSB, CLDN16, CPB1, PNLIP, SLC13A2, and SLC14A2—that experienced significant changes in evolutionary constraint alongside changes in carnivory score...
  3. .... First, we adapted and applied a phylogenetic modeling approach to quantitatively compare epigenomic signals at orthologous regulatory elements and identified thousands of promoter and enhancer regions with differential epigenomic activity in mole-rats. These elements associate with known mole...
  4. .... The color legend is as shown in D.The inferred methylation states in ancestral species indicate an increasing proportion of hypomethylation in the orthologous along each branch of the phylogenetic tree (Fig. 2C). We estimated that HMRs made up 7.0% of the orthologous in the last common ancestor of the seven...
  5. ...mammalian RNA-seq data have been used to study the evolution of 1:1 orthologous (single-copy) genes (Brawand et al. 2011; Warnefors and Kaessmann 2013; Necsulea and Kaessmann 2014) and some specific aspects of paralogs (Chen and Zhang 2012; Rogozin et al. 2014), the evolutionary and functional relevance...
  6. ...of OR genes among multiple mammalian species is not straightforward for three main reasons. (1) The number of genes for inferring orthology and paralogy is very large. (2) Orthologous relationships between genes from two species are usually not one-to-one; they can be multiple-to-multiple or zeroto...
  7. ...-sequence-based metrics of gene tree correctness and benchmarked a number of tree methods. The TreeBeST method from TreeFam shows the best performance in our hands. We also compared this phylogenetic approach to clustering approaches for ortholog prediction, showing a large increase in coverage using the phylogenetic...
  8. ...and Griffiths-Jones (2011) for miRNA annotation from RNA-seq data]. As a result, miRNAs in our data set are supported by 90% or more reads that map only to miRNA genes and are not enriched with repeated elements (Supplemental Table S8). Inference of miRNA clusters and families MiRNA genes within 50 kb of each...
  9. ...(24 repeats) (Supplemental file 1, S5), the most recent phylogenetic group we considered was ‘‘Primata.’’ This group was composed of human repeats that were also present in chimpanzee and rhesus macaque but absent from the rest of the mammalian and vertebrate orthologous proteins (157 repeats). Given...
  10. ...phylogenetic inference. Our trees show that species-specific V1R subfamilies are common throughout the entire mammalian phylogeny and are especially apparent in species with large V1R repertoires. Most V1Rs we identify are the product of duplication since divergence from any other species in our study. In fact...
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