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We now consider a linear representation of the data with a coordinate system where the mean (langlemathbf{y} rangle) sets the origin and m is the direction of the line.
Molecular clock calibration sets the origin of Sylvia to ~20 Ma, with diversification of extant lineages beginning at 19.4 Ma.
Notice that sets the origin of all the child haplotypes, therefore, since all preceding homozygous loci can have the same origin as locus t1.
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In what follows, we will set the origin of the altitudes at the mean substrate level.
Set the origin of the coordinate system at the centre of the rod.
We set the origin times of the synthetic hypocenters to the same times as the actual ones.
Let us set the origin of the breeding value at its average in the parental distribution, i.e. ∫ ℝ y p 0 (y ) d y = 0.
We considered models with two linear phases, before and after the onset of terminal decline and set the origin at 2 years before death.
Slice timing correction was performed using the middle slice as the reference, and the slices were re-orientated setting the origin at the anterior commissure and setting the horizontal axis to run along the anterior commissure-posterior commissure line.
Here a* designate the complex conjugate of a, i = −1 and we have set the origin of the breeding values at its mean in the parental population, i.e., ∫ ℝ y p 0 (y ) d y = 0.
We set the origin of the Liolaemus crown group radiation (beginning with the latest common ancestry between the subgenera Eulaemus and Liolaemus sensu stricto) at 19.25 million years ago (Mya).
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CEO of Professional Science Editing for Scientists @ prosciediting.com