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Strikingly, most of the epitopes predicted by our method mapped to regions predicted to be immunogenic based on independent criteria (Figure 4A) which offers additional confidence in the epitopes predicted by our method.
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Even though millions of genome-wide conserved motifs were identified by our method, mapping of these motifs to the promoter sequences results in constrained conserved genomic regions.
With this read correlation method, 538 scaffolds (96.9% of total assembly sequence), including 352 scaffolds not mapped by the first method, mapped to within approximately 5 cM of a marker in the consensus scaffold map (Table S3).
(g) Ghost map by our method.
While the average time taken by our method (inclusive of calculating saliency maps) is s for registering a pair of volumes, the corresponding average time for the method in [20] was s.
The mapping obtained by our method results in a smaller delta size of two triples.
We do not have the ground truth of the camera laser extrinsic parameters, but the mapping results by our method (red dotted line) are more reasonable.
These tests show that the approximated depth map obtained by our method provides the best 3D visual perception and the visual picture quality of the results by our technique is higher than that of the existing method.
In "Evaluation" section, we describe the experiments conducted for evaluating the map consistency estimated by our method.
We demonstrated the utility of this approach by accurately determining the bin map positions of the majority of the large sequence contigs from each genome sequence and validated our method by mapping single sequence repeat markers derived from sequence contigs on a full mapping population.
We illustrate our method by mapping a generic automotive used fuel pump controller (FPC) design to LUT format.
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