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In filter bank multicarrier (FBMC) methods, this problem is resolved, simply, by using filters with well-attenuated stopbands, [3].
Because of the limited number of therapeutic methods this problem is one of the most urgent challenges in biology and medicine [ 1– 3].
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As for the new method, this problem is solved by introducing external markers determined by contextual information.
We can find the best seam (the shortest path) via dynamic programming method, this problem can be common in graphs.
With our method, this problem is eliminated because the starting material is a CVD-grown single-crystalline 2D superlattice.
Using the compact finite difference method this problem can be recast as an ordinary differential equation initial value problem.
Although not fundamental to the standard method, this problem is exacerbated by its unfailing production of large numbers of significantly enriched terms.
Although, a few samples like JPN15 (DPB1*05:01:01/DPB1*135:01 and DPB1*25:01) were not fully resolved by the multiplex PCR-NGS method, this problem could be solved in future by determining the full gene nucleotide sequence for the DPB1 gene with the *25:01 allele.
Existing methods concerning this problem can be categorized into two aspects, the centralized method and the decentralized method.
The proposed methods solve this problem as explained below.
The above methods overcome this problem by transformations of the objective function.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com