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Each group has four subgroups, and each subgroup is constructed based on a base sequence defined as u=[u(0),…,u(K−1)]T.
To achieve (21), we design a base sequence in accordance with the Chu sequence which is a polyphase sequence that has a perfect periodic autocorrelation property leading to a constant magnitude in both time and frequency domains.
Reference signal sequence ϑUE(k) of the data channel is defined by a cyclic shift α UE of a base sequence, i.e., ϑ UE k = e j α UE k ⋅ ϑ ¯ k, 0 ≤ k < M sc RS, (1).
Sequence positions except the binding sites are assigned by searching for a base sequence that will fold into the target structure designed in the previous step using RNAinverse[28] or RNAdesigner from RNAsoft[31], with a non-binding pseudo-base (N) being assigned to all positions in the binding region.
Off-target effects arise when an introduced RNA has a base sequence that can pair with and thus reduce the expression of multiple genes.
Sequence space is defined by a set of allowed mutations off a base sequence, per sequence position, per residue.
Similar(52)
This is due to the complexity of partially converting a 4 base genome sequence to a 3 base sequence.
Let A and B be a protein amino acid sequence and an RNA base sequence, respectively.
In the future, such a 60 base sequence could be manufactured.
If all four bases were present, the location was written to a 5 base sequence array of 1020 possible combinations.
The criteria were met by a 201 base sequence containing 11 CpG sites in the 5'UTR (-559 to -359) of the 5-exon/4-intron GLTP gene.
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