Exact(14)
The novel hinge-binder tethered 1,2,3-triazolylsalicylamide scaffold was effectively assembled by Cu(I -catalyzed azI -catalyzed,3-dipolazide alkynetion (CuAAC).
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.
Previously, Illumina sequencing of transcriptomes for organisms with completed genomes confirmed that the relatively short reads produced can be effectively assembled and used for gene discovery and comparison of gene expression profiles [ 21, 22].
Similar(46)
Up to now, effectively assembling micro biomimetic CaCO3 particles to form a functional material is still an important research topic.
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.
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 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.
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