Searching journal content for articles similar to Martı́n et al. 13 (5): 991.

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  1. ...alignments, profile hidden Markov models, and cross-references to G-quadruplex 3D structures. Examination of G-quadruplexes across functional genomic elements in different taxa indicates preferential orientation and positioning, with significant differences between individual taxonomic groups. For example...
  2. ...a genomic basis to study host-microbe interactions, and we demonstrate its utility in identifying candidate pathways in the bacteria affecting chemotaxis behavior and survival in the nematodes. Second, we generate nematode transcriptomes of P. pacificus nematodes on 38 bacterial diets and characterize 60...
  3. ...% similarity) and D. melanogaster versus D. virilis (62% similarity). In both species, genomic regions covered by metapeaks show levels of conservation intermediate between exons and random segments (Fig. 2A,B).View larger version: In this window In a new window Figure 2. Conservation of metapeak regions...
  4. ...the distribution of structural similarity with sequence identity at the genomic level and characterized the twilight zone. We also investigated enrichment patterns in human proteins that are structurally conserved with archaeal and bacterial orthologs. These results presented here showed an exciting new frontier...
  5. ...replication strategies and host interactions among Asgard-infecting viruses, with Opia representing an intermediate complexity within this spectrum.View larger version: In this window In a new window Figure 5. Comparative genomics of Asgardarchaeota MGEs. (A) Whole-proteome similarity network of MGEs from...
  6. ...diversity of bacterial genomic changes, including gene duplications and HGTs (leading to paralogs), homologous recombination, and large-scale gene insertions and deletions. We therefore performed our first benchmarks by comparing a pan calculated from 15 manually curated Salmonella enterica annotations...
  7. ...Tree: computing large minimum evolution trees with profiles instead of a distance matrix. Mol Biol Evol 26: 1641–1650. doi:10.1093/molbev/msp077 ↵Quinlan AR, Hall IM. 2010. BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics 26: 841–842. doi:10.1093/bioinformatics/btq033...
  8. ...contigs in a reference tree; assemblies were compared using the numbers of identified contigs at different taxonomic levels. Third, the numbers of conserved 16s ribosomal RNA (rRNA) and 16s rRNA clusters were used to evaluate the completeness of the metagenomic assemblies; bacterial and archaeal ribosomal...
  9. ..., as compared to not-depleted libraries. We estimated that one would need 3.5–4 times more sequencing data to achieve the same performances when using not-depleted libraries. By targeting the majority of genomic length (84%), the depletion allowed us to pour a large fraction of sequencing data on the single...
  10. ...from a nonrepetitive region.Over 1000 bacterial and archaeal s in RefSeq contain scaffolds mapping to human repeatsTo identify human repeats in nonhuman s, we searched profile HMMs from the Dfam database of eukaryotic repeats (Hubley et al. 2016) against all archaeal and bacterial s in RefSeq release v...
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