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Resolving the base of the nematode tree will require intensive efforts to locate other informative genes-ideally protein-coding-which can supplement evolutionary inferences from SSU data.
Future molecular studies of nematodes will need to incorporate phylogenomic methods in order to resolve longstanding questions regarding relationships at the base of the nematode tree.
We tested support for the alternative split patterns at the base of the nematode phylogeny using the Shimodaira-Hasegawa log likelihood ratio test [ 32].
It appears unlikely that single-gene phylogenies using the conserved 18S gene will be useful for confirming the branching order at the base of the nematode tree-future efforts will require multi-gene analyses or phylogenomic methods.
Moreover, neither is attracted to the base of the Set8 clade, or even to the base of the nematode clade, but rather to individual sub-clades within the nematodes.
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With the presence/absence of the species described above, or with protein/codon aware nucleotide alignment, the relative positions of all other nematodes do not change in any case tested, only N. aberrans has different positions at the base of either the cyst nematode clade or the root-knot/pratylenchus nematode clade.
In this analysis N. aberrans was more similar to either M. incognita or G. pallida than they are to each other, supporting the position at the base of the cyst nematode root-knot nematode root-knoto
Soil food web indices, based on the composition of the nematode fauna, were calculated to infer soil food web condition.
The structure of the nematode community degenerated and the role of nematodes in soil food web was weakened in the agro-ecosystem after long-term drought.
The larvae of the nematode Anisakis simplex parasitize seafood.
The purified Hasp killed the juveniles of the soybean-cyst nematode (Heterodera glycines) and degraded proteins of the nematode cuticle.
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