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In order to examine the stramenopile "paraphyly" in GapC1 phylogenies, an improved sampling of stramenopile GapC1 genes is needed.
Several years ago, an improved sample preparation kit was introduced [ 14].
We argue that such a diversity structure calls for specific improved sampling strategies in future microbial community surveys.
Nonetheless, we anticipate that continued improvements in instrumentation, combined with improved sample preparation, will provide additional sequencing depth and speed in the future and the present study illustrates how this can be used to produce a more comprehensive mapping of gene expression and regulation during fundamental biological processes.
This suggests that lack of independence could explain the disparity between the position and monophyly of mites when combined analysis results are compared with exclusively molecular analysis, as per Wheeler & Hayashi [ 9] and, mainly due to their improved sampling effort, in Giribet et al [ 10] and in our own analysis employing unconstrained direct optimization.
The improved sampling of butane rotamers in states 0 and 1 by using sesTI is evident across λ and the replicas.
The combination of improved sample preservation approaches and advancements in the field of electron tomography and high-resolution fluorescence microscopy are expected to enlighten kinetochore organization at increasing resolution.
With this improved sample, the atpI phylogeny was no longer in significant conflict with the organismal tree; instead, relationships among Triticum, Oryza, and Saccharum/Zea were entirely unresolved under an all nucleotide position ML model (Additional File 6).
Direct analysis under imaging conditions is typically limited to proteins below 30 kDa (Francese et al. 2009), but can be increased in some cases by improved sample preparation techniques (Franck et al. 2010; Leinweber et al. 2009) and/or instrumental modifications (van Remoortere et al. 2010).
The multiple inverse sampling may be viewed as an improved version of quota sampling in some sense.
We describe an improved method for sampling CSF in rats that is easy to perform.
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