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This can be characterized by the following: y ∈ ω τ, Σ ( B ) if and only if there are sequences { x n } ⊂ B, { σ n } ⊂ Σ, { t n } ⊂ R τ, t n → ∞ such that U σ n ( t n, τ ) x n → y ( n → ∞ ).
We shall say that x is of type 1 if there are sequences of positive integers { k m } m ≥ 0 and { i m } m ≥ 0, the first one strictly increasing, such that for all m ≥ 0 we have i m ≥ s k m and card ( S k m, i m x ) < card ( S k m + 1, i m + 1 x ) ; here and henceforth, for a finite set P, we denote by card ( P ) the number of its elements.
More sequences are added to the group if there are sequences in the two proteomes that are closer to the corresponding seed ortholog than to any sequence in the other proteome.
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How does one rule out other possible conserved interactions even if there are sequence differences in the binding pocket?
However, the trimming procedure sometimes fails if only part of the adaptor is contained in the read or if there are sequencing errors in the adaptor sequence.
Additionally, the mapped small RNAs should be located in the stem region of the folded RNA, and a higher probability score is awarded to a given candidate if there are sequencing reads corresponding to the predicted miRNA* region.
How does one rule out other possible conserved interactions even if there are sequence differences in the binding pocket? 3) The binding pocket conformation has been assumed to be very rigid while attempting to illustrate that L-amino acid analogs would be sterically excluded.
(z=R^{infty} u,v)) if and only if there is sequence of successive approximations of R starting from ((u,v)) that converges to z. for all ((u,v in mathrm{Graph}(R)), we have (d u,R^{infty} u,v))leq Psi (d u.v))).
We considered the impact of IFs on the rate of reporting if variant frequencies were to change or if there were sequencing errors or errors in the subsequent bioinformatics analyses and database annotations.
Sequences were only included if there was sequence alignment of more than 100 bp, thus some species (e.g. Poephila acuticauda) identified to be in the top ten closest matches to one of the Nesospiza alleles were not included.
If Y is not normal, then there are sequences ( x n ) in X such that x n ?
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CEO of Professional Science Editing for Scientists @ prosciediting.com