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This finding points to the fact that meta-analyses, due to an enhanced statistical power, may disclose differentially expressed genes that are missed by analyses of single study gene expression data sets.
At the plastid level, the monophyly of chromist plastids is supported by analyses of single genes [ 28], of small numbers of concatenated plastid genes [ 12, 29], and of larger datasets of plastid-associated genes, i.e. plastid and nuclear-encoded plastid-targeted genes [ 30- 35].
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The comparison of Figure 2A, B also shows additional ORs, which were not detected by the analyses of single taxon pairs.
Interestingly, recently this supposition was partially confirmed by SSR analyses of single S0 plants form five Eastern European open-pollinated varieties.
By thorough analyses of single molecule trajectories, we show caspase-3 activation in a drug-treated chronic myeloid leukemia (K562) cancer system as early as 4 and 8 h with greater sensitivity (2- and 4-fold, respectively) than conventional reagents.
The monophyly of enteromonads was not rejected by analyses of any one single gene.
Cytogenetic and molecular responses suggested that the two disorders arose independently, which was corroborated by genotyping analyses of single-cell-derived colonies.
Third, we inferred phylogenetic relationships and major morphological evolutionary trends within the section Calochroi by integrating molecular phylogenetic analyses of single and combined DNA sequence datasets with morphological, chemical and ecological features.
To complement the analyses of single genes by sequential ChIP and cryoFISH, we investigated genome-wide correlations between S5p and H2Aub1 or S2p.
Second, the fission yeast cells tend to form multimers by sticking together, thereby perturbing flow cytometric analyses of single-cell behaviour and of cell-cycle kinetics.
The quantitative analyses of single-labelling data were confirmed by the qualitative analysis of double-labelling experiments (Fig. 8).
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