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The rapid-prototyping procedures we describe are simple, employ readily available equipment, and provide a link between computer-aided design and self-assembled functional nanostructures.
We demonstrate our strategy using the Illumina GAII technology although the procedures we describe could be applied to other sequencing platforms that can generate paired end data.
The procedures we describe below for IBC may be helpful in the standardization of diagnoses of other diseases with a clinical component.
These results are consistent with the interpretation that M5-DLO molecules located in the inner leaflet of flippase-equipped proteoliposomes are flipped to the outer leaflet where they are captured by Con A. The data imply that TE contains M5-DLO flippase activity that can be functionally reconstituted through the procedures we describe.
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We applied the procedures we described earlier to the same genotypes as before, averaging now the number of modules (FCSs) rather than the number of reactions in these modules.
To investigate this possibility, we sequenced a 501-bp stretch of the VP7 gene (nt 79 579, amino acids [aa] 11 177) from 4 of these strains, using procedures we described elsewhere (4 ).
To present a detailed description of the procedure, we describe the procedure of calculating singular stress fields and stress intensities of co-cured double lap joints with a wedge that consists of carbon fiber reinforced plastic composite and steel adherends.
As a paradigm of our procedure, we describe the case where the transported form is CQ+.
The procedure we describe removes these costs.
Then, the procedure we describe above reduces to the standard K-means clustering procedure.
The procedure we describe is technically demanding, with a risk of complications such as joint penetration and neurovascular injury.
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