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The initial condition of finding p 0 assumed as an initial Lebanese fraction of the WES1 marker is specified by requiring P (j, 0 ) = { 1 where j = ⌊ p 0 N ⌋ 0 elsewhere.
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As a result, the physical positions of 3,704 markers were specified.
An equal population recombination rate (2Nr) of 1 between adjacent markers was specified.
The remaining markers are specified to be random draws from a Student t distribution with key hyperparameters being degrees of freedom v and scale s.
As a sensitivity analysis, a linear model with interaction variables of key clinical markers was specified to test for statistical prediction power of the utility difference.
However when the prior for the marker effect is specified as a t distribution, its full-conditional is not of a known form.
No payment structure is specified.
Then the condition is specified.
Since all marker positions were specified as whole numbers, exactly 166 positions were tested per chromosome per run.
It is possible, however, that this processing allows the position of discrete markers to be specified.
Since quantitative measurements of candidate markers in large and well defined clinical samples is central to the validation effort, criteria for the selection of the source material as well as the criteria for validation of the candidate markers must be specified.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com