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All predictors were used for the regional scale analysis, predictors in bold were selected for the local scale analysis (for more information see Appendix I).
Driver lines shown in bold were selected for more detailed experiments.
Genes highlighted in bold were selected for validation by real time PCR (see Table 6).
*Genes in bold were selected for candidate gene analyses by qRT-PCR.
Genes in bold were selected for candidate gene analyses by qRT-PCR.; # marginal signal intensity; NCBI, National Center for Biotechnology Information GBB, GenBank.
Note: The genomes which are highlighted in bold were selected for the analysis using 16S rRNA sequences and the phylogenetic tree for these cases is provided in Figure 2.
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SEC fraction highlighted in bold was selected for further analysis.
Genes in bold were selected by more than two studies.
The genes with black bold ID were selected for qRT-PCR analysis.
Genes with black bold ID were selected for qRT-PCR analysis.
Some variables available in the MHCR were excluded for the validity control, such as variables regarding the postpartum period and variables with no corresponding data in the medical records (e.g., the variables of self-reported health before, during, and after pregnancy).> -wrap-foot> Variables presented in bold text were selected for the comparison of data in medical records and in MHCR.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com