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For a single mapping, we find from Theorem 2.1 the following result.
For a single bifunction and mapping, we find from Theorem 3.1 the following.
If T is a quasi-ϕ-nonexpansive mapping, we find from Theorem 2.1 the following.
Then { x n } converges strongly to x = Q F f ( x ), where Q F is a sunny nonexpansive retraction from C onto F. Proof Since ( I − T ) is an α-inverse strongly accretive mapping, we find from Theorem 3.1 the desired conclusion.
Thus, when correcting chicken sequence assembly errors by RH mapping, we find that all markers from a given quail linkage group correspond to one chicken chromosome.
With 2D-trait mapping, we find that the co-expression patterns between them and LEU2 also change as the genotype of LEU2 changes.
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Using the program Bowtie35 with 100% identity to a minimum length of 50 bp and with '-m' set to 1 to ensure unique mapping, we found that 73% of the high quality reads mapped uniquely to the predicted ORFs (Supplementary Table 4).
By immunoblotting of immunopurified and reduced vWF and monoclonal antibody epitope mapping, we found that vWF was degraded after thrombolysis, especially after SK, as indicated by the higher values of two plasmin-generated fragments of 176 and 145 Kd.
From this mapping, we found twelve SPL use case templates and observed the need not only for the application of these templates in real SPL but also for supporting tools.
Additionally, during the process of mapping, we found that two previously reported SNPs required a new position on the tree.
Using Ensembl Biomart ID Mapping, we found 15,181 genes that could be considered human disease genes.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com