These results demonstrate that IQ-motifs are viable lead sequences for the identification and optimisation of novel anti-microbial peptides.
A PCR identification system targeting 23S rDNA sequences for the identification of eight streptococcal species relevant to animal infections (Streptococcus agalactiae, S. bovis, S. canis, S. dysgalactiae, S. equi, S. porcinus, S. suis and S. uberis) was developed.
This study illustrated the utility of COI and cytb gene sequences for the identification of the vertebrate hosts of the tsetse fly species.
At the species level, ITS2 sequences correctly identified 91.9% of 12,221 animal samples, whereas the success rates of using ITS2 sequences for the identification of 34,676 dicotyledons, 11,598 monocotyledons, 946 gymnosperms, 42 ferns, and 3,528 mosses were 76.1%, 74.2%, 67.1%, 88.1%, and 77.4% at the species levels, respectively (Table 2).
These miRNAs were defined as a reference set of miRNA sequences for the identification of potentially conserved miRNAs in Boechera.
The complete list of 529 genes was used to extract promoter sequences for the identification of putative TFBSs.
In a previous study we presented an assay for targeted mRNA sequencing for the identification of human body fluids, optimised for the Illumina MiSeq/FGx MPS platform.
The recent paper by Shah et al. [15] also used DNA sequencing for the identification of seven subspecies of M. chelonae/abscessus in their series.
Nevertheless, T2-WI has been assumed to be the dominant sequence for the identification of PC in the TZ when interpreting imaging findings of a mpMRI exam [42, 43].
Here we demonstrate the utility of two metagenomics-based strategies, a pan-viral microarray (Virochip) and deep sequencing, for the identification and characterization of 2009 pandemic H1N1 influenza A virus.
If relevant, it will also be sequenced for the identification of new variants important for outcome.
