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Analysis of DNA extracted from paraffin-embedded sections gave similar results, indicating that archived tissues can also be analyzed using this assay.
The periods and the diameters of the interpores can also be analyzed using image processing.
Potential biomarkers can also be analyzed using the database by the combination of average rank score (ARS) and marker evaluation score (MES) (Wang et al., 2015).
Any system characterized well enough to construct a compartmentalized model can also be analyzed using the nested approach.
In contrast to the microarray-based methodology used in the HuGE Index database, gene expression can also be analyzed using the tag-based techniques.
Data from studies with more complex designs can also be analyzed using analysis of variance (e.g. see Armitage and coworkers [ 6] or Montgomery [ 5]).
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The frequency and location of recombination sites on individual chromosomes can also be analyzed by use of antibodies to the mismatch repair protein MLH1 (Baker et al., 1996; Marcon and Moens, 2003; Sun et al., 2004b) combined with cenM-FISH to identify individual chromosomes (Fig. 3).
The products of NASBA can also be analyzed in a quantitative way using a NucliSens® reader and internal standards (van Gemen et al, 1995; Bustin, 2000), however the NucliSens® reader detects amplified products at an end-point unlike real-time PCR that detects products as they are generated.
The released sugars during hydrolysis can also be analyzed for simple sugars or oligosaccharides using standard high performance liquid chromatography or mass spectrometric methods as previously described [ 24].
Furthermore, the necessity of using robust modeling methods for the system can also be analyzed.
Large-scale structural reorganizations involved in the biological functions of proteins can also be computationally analyzed using either normal mode analysis (NMA) or principal components analysis (PCA) [47].
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