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We further require Cv(x) and Ci(x) to be outside of the spinodal (unstable) regime.
We further require in the simulations that simultaneously active links do not interfere.
We further require that P i ∈ ∂ Ω h ⟹ P i ∈ ∂ Ω where P i ( i = 1, …, J ) is the vertex set associated with the triangulation T h.
Hence, we further require the coded packet to belong to a set of U s maximal cliques that together cover all the data packets.
In fact, we further require some component of negative pressure, with ω < − 1 3 Open image in new window, to realize the acceleration of the universe.
We further require that P i ∈ ∂ Ω U h ⟹ P i ∈ ∂ Ω U where P i ( i = 1, …, J ) is the vertex set associated with the triangulation T U h.
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We further required the presence of 250 base pairs on either side of the putative SNP in FV-1 to avoid potential poor quality SNPs at contig ends.
To retroactively measure the progress of human genome annotation, we further required a gene annotation source providing access to releases over a multi-year period.
We further required that 250 base pairs on either side of the putative SNP in the FV-1 sequence be present (to avoid SNPs at the ends of contigs where sequence quality tends to be poor).
We further required compatible chest imaging documenting an infiltrate(s).
During the two processes, we further required the drug-target associations with Score_S ≥ 3 in WinDTome.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com