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The overall difference for all samples is defined as Eg = 1 N ∑ i = 1 N ∥ S i − S i ∗ ∥.
According to the classic Williamson-Hall method and its subsequent variations [19, 20], the differential strain of samples is defined as (1).
where the root mean square value (RMS) of a signal matrix M ∈ K Ch × S consisting of Ch channels and S samples, is defined as RMS ( M ) = 1 Ch · S ∑ ch = 1 Ch ∑ s = 1 S M ( ch, s ) 2. (14).
The test statistic, a score function, in large samples, is defined as: Z = ∑ij Tij Xij−E Xij))/Var(S 1/2∼N 0,1), where E Xij) is the expected value of the coding function for the offspring genotype, conditional on the parental genotype and parental/offspring phenotypes, which are assumed to follow Mendelian segregation under the null hypothesis.
The group with more DCM samples is defined as positive and the other group is negative.
Classification accuracy θ test on the test samples is defined as the percentage of the correctly classified samples.
Similar(51)
Foreground samples are defined as the skeleton regions of confident reconstruction segments.
Background samples are defined as the non-skeleton regions surrounding the confident reconstruction segments.
Samples were defined as proteolytically active when the difference of the absorbance readings was ≥0.03 units.
Samples were defined as positive with an OD450 nm of ≥0.8, negative with an OD450 nm of ≤0.2, and equivocal with an OD450 nm between 0.2 to 0.8.
These samples were defined as stubble; the heterogeneous plant compartment below the defoliation height which includes fully expanded leaf sheaths plus basal immature parts of expanding leaves.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com