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We have developed CYNTENATOR, a progressive gene order alignment software, to identify genomic regions of conserved synteny over a large set of diverging species.
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Further studies should now be engaged at the inter-organismal level in order to explore the function of this large set of rapidly diverging genes induced here in the allorecognition context.
For most metazoans this is a fast and simple strategy, but due to highly diverged mt gene order in ascidian species, a large set of forward and reverse primers needed to be tested to find the optimal ones for A. aspersa.
For example, we have identified a large set of LCNS among birds, and we find many more conserved regions between these two taxa than we found between human and mouse, which diverged approximately at the same time.
Based on a large set of human paralogous transcription factor pairs, we show that when the DNA binding site motifs of transcription factor paralogs are similar, the expressions of the genes that encode the paralogs have diverged, so in general, at most one of the paralogs is highly expressed in a tissue.
This being the case, it becomes obvious that the likelihood of parallel changes drops concomitantly with the decrease of the overlap between the covarion sets of diverging lineages.
This is the largest set of codes.
Whereas only one or a few loci are required to resolve the relationships among a set of recently diverged species, much larger amounts of comparative data are needed to reconstruct ancient branches of the tree of life.
It is also seen that for the case of converging tapering, it has a larger value as compared with the case of diverging tapering and non-tapered arteries.
We found that a large number of paralogs diverging between coding and noncoding RNA (fig. 8 B).
But here the two sets of protests diverge.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com