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When liquids are applied into the sparse SWNT forest and dried, the surface tension of the liquids and the strong van der Waals interactions effectively assemble the nanotubes together to near-ideal graphitic spacing.
These initial results suggested that Hapler can effectively assemble haplotype regions, however the inclusion of only a single outgroup sequence limited the generality of the conclusions.
These simulations indicate that the novel methods employed by Hapler effectively assemble correct haplotype regions, and that the quality of results produced will scale with the quality of future input data: as datasets grow to contain longer reads and fewer sequencing errors, more correct and complete haplotypes will result.
Furthermore, as has been shown for several bacterial ClpC orthologs [ 91, 93, 94], clpC1 could compliment the activity of clpC2 (acting dependent or independent of adaptors) by stabilizing and preventing aggregation of newly synthesized, unfolded proteins; a function that is essential to effectively assemble (or dispose of) large multimeric complexes in the chloroplast.
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Up to now, effectively assembling micro biomimetic CaCO3 particles to form a functional material is still an important research topic.
The novel hinge-binder tethered 1,2,3-triazolylsalicylamide scaffold was effectively assembled by Cu(I -catalyzed azI -catalyzed,3-dipolazide alkynetion (CuAAC).
We then showed that three of the scaffolds from v4.1 (34, 34, 143) were tightly linked to the ruby locus, thus effectively assembling the scaffolds at this locus.
These results suggested that the transcriptome sequencing data from A. racemosus were effectively assembled, which was further validated by the high proportion of unigenes matched with known proteins.
As with other recent studies [ 5, 7, 15, 16], our results indicate that short reads from 454 sequencing runs can be effectively assembled and used to readily characterize the gene space of non-model organisms.
Studies using transcriptome sequencing for organisms with complete genome sequencing have confirmed that the short-read products of NGS can be effectively assembled and used for gene discovery and comparison of gene expression profiles.
Consistent with these reports, the results from this research also suggested that short reads from Illumina sequencing can be effectively assembled and used for gene identification and SSR marker development in non-model organisms.
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CEO of Professional Science Editing for Scientists @ prosciediting.com