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All samples were categorized into one of the 5 molecular subtypes with the highest predicted probability, assuming that probability exceeding the threshold of 0.5.
All samples were categorized according to a subjective analysis of the levels of autofluorescence from photosynthetic pigments (Table 2) and the categories 'low', 'medium' and 'high' were given to describe the densities of symbionts.
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To study the age-wise prevalence, all the PCR positive samples were categorized into five age groups (Table 2).
Samples were categorized as quartzite group and carbonate group according to ASTM standard 295.
Voice samples were categorized from low to high conception risk based on menstrual cycle phase and empirical pregnancy data.
The remaining 18 samples were categorized into 5 GII genotypes including GII.4 (11), GII.8 (2), GII.1 (2), GII.5 (2) and GII.2 (1) as shown in Fig. 3.
For analysis, tissue samples were categorized into the following groups: injured meniscal site (IM), non-injured meniscal site (NIM), synovium 'nearest' the lesion (NS), and synovium from the opposite knee compartment, 'farthest' synovium (FS).
The genes that were found to be differentially expressed between the two samples were categorized into Gene Ontology (GO) categories and fell into three major groups: cellular component, molecular function, and biological process.
The samples were categorized as two groups, normal skin or benign nevi (normal/benign) and melanoma.
Samples were categorized into 4 habitat types: fecal, ocean, lagoon, and creek (Figure 1).
These samples were categorized into three groups: negative expression; low expression (<10); and high expression (>10).
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CEO of Professional Science Editing for Scientists @ prosciediting.com