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The result appears to be a connected series of analyses sharing at least a family resemblance with each other.
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Finally, our analyses share the limitations of the studies included in our review.
Genes included in the same clade based on parsimony analyses share similar structural characteristics.
Thus, in our analyses, shared components between many complexes (i.e. the hubs) are not more likely to be essential than non-hub proteins.
However, it should be noted that in the longitudinal analyses shared environmental influences were only observed in adolescence and not at age 30 32.
All the analyses shared a common design where temperature, species and strain factors were fixed and host genotypes and treatment replicates were included as random factors.
It is noteworthy that 10 species of Ascaridomorpha and 20 species of Rhabditomorpha included in our phylogenetic analyses share a common pattern of gene arrangement, GA3, in their mt genomes.
In the twin analyses, shared environmental effects were small and generally nonsignificant (accounting for 7%-97%-9%the variance in TOWRE scores; shared environmental correlation = 0.39), whereas nonshared environmental effects were somewhat larger and significantly greater than zero (accounting for 17%-25 17%-25e variance in TOWRE scores; nonshared environmental correlation = 0.36).
These possible next steps carry on in the spirit of Cyrface, RCytoscape, and Cytoscape3 apps, and will promote the creation of, and sharing of, custom network analyses, shared tools, and lead to fruitful collaborations across the hybrid community of biologists, physicians and programmers.
In summary, GSEA results from both 4/5- and 21-somite analyses share significant downregulation of the retinoic acid pathway as well as red blood cell genes, which serve as a positive control for the analyses; however, the two results differ in that the Wnt pathway is significantly upregulated in the 4/5-somite, but not in the 21-somite, analysis.
The trees inferred from the latter two analyses share a very similar topology with the ML-all tree (Fig. 2), except for the monophyletic clade composed of Cyanidioschyzon merolae and Galdieria maxima that is positioned with the Galdieria-A + -B lineage in the ML-protein tree.
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