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There are two complementary sources of information for dating ancient biological divergences: (1) physical historical remains (either paleontological or ichnological); and (2) molecular sequence differences among extant taxa, the analysis of which requires assumptions about the processes and rates of sequence evolution.
A total of 32 patients were investigated – of which five presented with the following apparent divergences: 1. CR: 98 bpm; MBP: 80 mmHg, in use of norepinephrine (NE); CVP: 12 mmHg; Lac: 1.6 mmol/l; SaO2: 98.1%; SvcO2: 54.9%; ΔPCO2: 5 mmHg; IVC: 24 mm; ΔIVC: 10%.
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What can be called the classical view goes back to antiquity, and represents a point of departure for later divergences.[1] To see knowledge about the natural world as falling under knowledge more generally is an understandable conflation.
Kullback Leibler divergences [9] is another measure for computing the similarity between two vectors.
In the field of higher derivative theories was introduced in order to get rid of ultraviolet divergences [26].
For example, duplicate genes, which are usually associated with highly consistent coding sequences but diverse biological functions, have only a weak correlation between rates of sequence and expression divergences [1].
We will call the two divergences JSM0 and JSM5 respectively.
Shallow intraspecific (average within species sequence divergence of 2.72, SE = 0.048) and deep interspecific divergences (9.4% SE = 0.05) between A. grandidieri and the other species.
Table 3 and Figure 1 summarize divergences (K2P distance) among specimens at various taxonomic levels.
Deep intraspecific sequence divergences (>2%) were detected in 20 traditionally recognized species.
Lineages A5 and F showed the highest within lineage sequence divergences (0.35% and 0.65%, respectively).
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