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Based on a Raman spectrum, residual strain, impurities, lattice distortion, and phase transformation of a sample can thus be estimated.
The whole sample can thus be separated into "genetic" EAs (European ancestry proportion > 0.5) and "genetic" AAs (African ancestry proportion > 0.5), according to the ancestry proportions in probands.
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The spatial samples can thus be readily expressed as follows [11]: (2).
The adhesive response of the samples can thus be grouped in three preload phases: i) at low preload only LP form contact with the probe resulting in and a low pull-off force, ii) at intermediate preload both LP and SP form contact with the probe and a high pull-off force occurs, and iii) at high preload, the pillars buckle and the pull-off force breaks down.
Lack of a priori defined sample size calculations leading to insufficient sample sizes and ultimately insufficient statistical power [73]; studies with an insufficient sample size can thus lose their ethical justification [74].
A hybridization temperature of 50°C results in comparably high signal intensities in the sample and can thus be employed for background problems when the activity of fluorescent proteins is not of importance.
This can be exemplified by an inspection of the specific results that the method yields for English: Of the 32 borrowings into English 18, eight are singletons and five have reflexes in almost all Germanic languages in the sample and can thus technically not be identified by the MLN approach.
Applying the above relationship, the ratio before PCR of sequences A and B in a given interest-sample (is) can thus be estimated as: <img src="http://journals.plos.org/plosone/article/asset?id=info?doi/10.1371/journal.pone.0011723.e002.PNG" class= inline-graphic"/> To solve the equation above, NCqs, Cqs and Es must be accounted for.
However, these isotopes have not been measured in GSR samples and can thus be neglected.
Second, the observed differences in sequence read density in common peaks are presumed to reflect the scaling relationship of ChIP-Seq signals between two samples, which can thus be applied to all peaks.
By throwing all 14 initiators into a test sample, Dr Shivji can thus identify which shark species it contains.Recently Dr Shivji has found stretches of DNA unique to subpopulations of sand tiger shark, and added them into the soup.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com