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Based on the mapping, we determined that V3 sequence variation accounted for neutralization resistance of approximately half the viruses tested.
By high-resolution genetic mapping, we determined that st67 disrupts the zebrafish homolog of sec63.
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To further analyze the quality of learners' interaction with MIC-O-MAP, we determined the productive value action (PVA).
By changing the sight angle of the high-resolution bathymetric maps, we determined the strike of the linear fault scarplet (yellow arrow in Figure 5b) and the sense of dip slip along it; the clearest fault trace located on the trenchward side of the pull-apart basin is downthrown on the north.
Using the values of the concentration map, we determined that most of the CaM molecules are part of molecular complexes.
Besides calculation of CBV maps, we determined the intensity time curve within the ROI with the highest rrCBV value.
For CIM on the consensus map, we determined the simple interval mapping LOD thresholds through 1000 permutations with a genome-wide error rate of 5%.
Using single-molecule maps that partially aligned to EBV reference maps and partially to the hg38 reference maps, we determined the EBV integration sites in all three samples.
Using a statistically obtained, high-confidence, stable nucleosome map, we determined the exact distance between the dyad of the +1 nucleosome and the TSS for all genes.
In the remaining 5 maps we determined the location of the imaging site relative to the barrel using alignment of vertical blood vessels.
To assess the coverage of this map, we determined the number of markers in each of the 34−69 1-Mb windows of D01-D13.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com