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Finally, several TCs – Cl000209 1 (61 ESTs) Cl000582 1 (18 ESTs) Cl001827:1 (5 ESTs) and Cl000731(2 ESTs) – show similarity to potyviral sequences, indicating that the sequenced library likely derives from virus-infected tissue.
From the figure we can not find any visible difference among the trends of these sequences, indicating that the forecast error growths at different analysis time are very similar.
However, the tests support the null hypothesis for the modern and putative contaminant sequences indicating that the rate of nucleotide misincorporation was the same (Two sample T-test T-Value = −0.42, P-Value = 0.688; Mann-Whitney test W = 1137.0, p-Value = 0.8588).
They all have predicted N-terminal signal sequences, indicating that the N-terminus is extracellular.
The observed effects take place even in the absence of donor plasmids containing attB sequences indicating that the effects are caused by the integrase enzyme directly.
However, we report here that orthologous pairs of TF DBDs almost invariably bound to the same DNA sequences, indicating that the binding specificity is very deeply conserved.
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The ab initio molecular modelling of such sequences indicated that the structure does not affect the predictions, as both sets present similar structures.
Phylogenetic studies based on partial RNA polymerase gene sequences indicated that the Venezuelan isolates were most closely related (75 95% identity) to the sapovirus Cowden reference strain.
Analysis of the 16S rDNA sequences indicated that the four strains were Donghicola sp. CT5, Bacillus sp. CT6, Alcaligenes sp. CT10, and Pseudomonas sp. ZS1 (Fig. 1c).
Analysis of EBV genomic sequences indicated that the majority of EBV miRNA nucleotide variants resulted from post-transcriptional modifications.
ITS sequences indicated that the collection zb1485 is unique and well differentiated from its sister taxon H. bulliardii.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com