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We evaluated the quality and quantity of short-read assemblies and proved that short-reads transcriptome assemblies are large in quantity and high in quality for further analysis, which can provide considerable utilities for non-model organisms.
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The average proportion of heterozygous genotypes per marker was comparable between the two assemblies except for chromosomes 2A, 3D, and 4A, where differences between the two assemblies were large.
Among competitive entries, 5 of the 11 bird assemblies were larger than the expected genome size (average ratio = 106.3%; Additional file 4).
In contrast to SaCld, both apo- and holo-LmCld form hexameric assemblies (Fig. 1), but with the interesting observation that the RZ-values of small fractions of holo-LmCld, with higher oligomeric assemblies, were larger, indicating more stable cofactor incorporation.
The 5 1 ratio aggregates, however, were slightly abnormal in appearance and size distribution (the populations of smaller aggregates and fiber assemblies were larger and smaller, respectively) compared to the lower ratios.
In other words, the reference gap size between fuel-assemblies is larger than the gap between fuel rods within a fuel-assembly.
Only one gap in either assembly was larger than 100 bp (in Platanus; Table 1).
This is not simply because the assembly is larger in size than others (there are four other bird assemblies which are larger in size).
The clustered region likely contains additional assemblies that are larger and have greater degrees of crosslinking that appreciably slow dynamics further.
Clearly, these assemblies are too large to fit inside a 1 2 nm gap between nanostructures.
These non membrane-bound assemblies are often large, occupying an intermediate length scale situated between the nanoscale of individual macromolecules and the microscale of cells.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com