Searching journal content for articles similar to Lin et al. 21 (11): 1916.

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  1. ...similar to ORF1p. (C) In the mammalian vertebrate RefSeq proteins, two protein-coding genes had alternative ORF1p-like exons. The amino acid sequences encoded by the final coding exons were similar to ORF1p. (D) Protein structures of the ORF1p-like amino acid sequence encoded by the noncanonical exons...
  2. ...in the strength of selection occurred along the long branches separating MHC-I-like1 and MHC-I-like2 from other sequences in MHC-I phylogeny, and (ii) whether the number and location of codons under positive/purifying selection differ among the three categories of genes.There was evidence of selection relaxation...
  3. ...have at least one G4 sequence per species, followed by bacteria with 6.6% and viruses with 2.2% (Supplemental Fig. 3). Furthermore, if we partition the genes into the two mutually exclusive sets of protein-coding and noncoding, we find in eukaryotic organisms an even higher median overlap of 25...
  4. ....9% of reads started or ended with an MspI cut site. As expected, DNA input fragments were enriched for functionally important areas of the , with 41% located within protein coding sequences, 18% in promoter regions, and 17% in CpG islands (Fig. 1D). As observed in RRBS (Gu et al. 2011), these DNA input...
  5. ...evolutionary background of the genomic regions where each element is located, it is necessary to take gBGC into account when testing for lineage-specific acceleration, especially when detecting positively selected elements.MethodsSpecies informationThe final collection of s used in this study contained 201...
  6. ...% of the protein-coding genes overlapped with at least one other protein-coding gene (Chen et al. 2019). Most of the time, the overlap involved a noncoding sequence (5′ untranslated region or UTR, 3′ UTR or intronic sequence) and sometimes only a few nucleotides were involved at the 3′ or 5′ end of the genes...
  7. ...of completely sequenced s, the large majority of which (>90%) originate from prokaryotes (Reddy et al. 2015). The accurate annotation of all protein-coding genes (interchangeably used with CDSs from here on) is essential to exploit this genomic information at multiple levels: from small, focused experiments, up...
  8. ...to the genomic target site (protospacer), which also requires the protospacer adjacent motif (PAM) at the 3′end, comprised of an NGG sequence (whereby N is any nucleotide and G is guanine). In addition to the target complementary sequence (spacer), the gRNA also contains a constant CRISPR RNA (crRNA) sequence...
  9. ...genome sequence. Within protein-coding regions, the redundancy of the genetic code can, in principle, allow for the overlapping encoding of signals in addition to the amino acid sequence, but it is not known to what extent genomes exploit this potential and, if so, for what purpose. Here, we...
  10. ...capacity. In addition, other possible scenarios of exitron origin can exist that are not tested by this approach and can be explored in future. As exitrons are internal regionsof protein-coding exons, selective pressure would prevent substitutions that disrupt their coding capacity, while favoring those...
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