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We construct a binary contiguity weighting matrix (mathbf{W}) in which the (i,j) elements (corresponding to the relative position of region (i) with respect to region (j)) take value 1, (bar{w}_{ij}=1), if the involved regions share their borders, at least partially; and take value 0, (bar{w} _{ij}=0), otherwise.
Hence, we assign two different indices to each candidate according to Starting Position Order (SPO) and Ending Position Order (EPO), i.e., for two candidate regions r and s, assuming b(r) gives the starting position of region r, and e(r) gives its ending position, we have: r ≤ SPO s, if b(r) < b s), or if b(r) = b(s) & e(r) < e(s).
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An alignment between PPI-1v from the lineage A isolates and the highly virulent isolates shows the relative position of regions 3 and 4 and is compared with the region in ATCC 700669 and G54 (Fig. 3).
The position of regions 1 through 3 are labeled to the right of each germarium.
Size and position of regions are drawn to scale relative to the ICD.
The size of the regions was image specific because of varying breast sizes, but the relative position of regions across images was similar.
We depicted the position of regions, length, and graphical view of such regions in Figures 2(c), 2(d), 2 e), and 2(f).
This table also details size and position of regions of LOH, intervals with near 0.5 Col-0 allele frequency and intervals showing RF less than 1 cM/Mb.
We analyzed the relative position of regions similar to RNases, RTs and phage-recombinases with respect to the region found to be homologous to the LAP2alpha domain in the Western painted turtle.
The inset ('map of imaging locations') shows the relative positions of regions i, ii and iii.
The purpose of the present study was to develop such an active contour method and to validate it against results obtained from manual positioning of regions of interest.
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