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Prediction of fold-back structures and energies performed with the DINAMelt server indicated that the stem-loop structure for many sequences were stable (with low folding energy) (Table S2) and lacked large internal loops or bulges.
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From the analysis of UV melting results, thermodynamic profile was computed and it was concluded that all the sequences are stable at 37 °C.
Our study shows that heterologous RTBV sequences, which do not bear any similarity to the predicted siRNAs, can substitute for the CaMV sequences involved in formation of stem-section 1 without any notable effect on CaMV infectivity and these sequences are stable over several passages.
Furthermore, we did not find evidence of entrainment of a neural oscillation at the stimulation frequency, as the shape of the transient ERPs obtained from jittered sequences was stable, and there was no evidence of additional activity outlasting the stimulus train.
We observed that several glycoprotein gene sequences are stable from primary to recurrent infection.
When DOG-1 is functional, G-rich DNA sequences are stable and deletions affecting these regions are not observed [ 4, 5].
These data suggest that SFV sequences are stable in nonhuman primates and can be used for several macaque species to mark an individual's geographic origin.
We have studied lesional virus isolates from humans with genital HSV-2 infection and observed that several glycoprotein gene sequences are stable from primary to recurrent infection.
As a consequence, the inverse nodal problem defined on the partition set of admissible sequence, is stable.
Therefore, a found sequence is stable for a longer time and transactions are scheduled when they are likely to have a good channel.
Suppose DNA sequence is stable under the stimulation treatment, then the site to which a transcription factor can potentially bind is considered to be invariant.
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