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Although the length will likely increase in the near future, extending our procedure to process longer reads is straightforward because our algorithm runs in O(n log n -time for processin -times oforny length n as stated in the processingubsection.
As stated in the previous subsection, considerably variable motif profiles could be observed for individual species.
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This subsection is devoted to the proof of the existence and uniqueness results stated in the previous subsection.
The situation stated in the previous subsection can be qualitatively or quantitatively changed by adopting disk parameters different from MMSN.
In Reaction d, although PA-O 2 Hs are rather difficult to obtaine via Reaction c, as stated in previous subsection, it can be generated without energy barrier by attaching the terminal O of HO2 directly to the carbon radical site of PA, Reaction h.
There are core and attachment proteins, as stated and analyzed in the previous subsection.
This result is arrived at using a perturbation analysis exactly as considered in the previous subsection.
We proceed similarly as in the previous subsection.
In addition, we have performed experiments with 39 yeast genomes as in the previous subsection.
This is done exactly as in the previous subsection (Switch) for the transcriptomic entropy, but now the gene expression data are replaced by DNA copy number data.
To clarify this scenario we use the reaction with complex transfer state explained in the previous subsection, renaming the species as R (for 80S_aatRNA_eEF2_GTP), P1 (for 80S_tRNA) and P2 (for eEF2_GDP), the site codon as c, and the variable criticalCodon as d, yielding (10) R(c{1 d}) -> P1 c = succ(R.c)) + P2; M(c=R.c).
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