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Patients who lacked these mutations were categorised as having the CYP2D6*1 (functional) allele.
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The investigated mutation is categorised as probably damaging (probability score more than 0.85), possibly damaging (probability score between 0.16 and 0.85) or benign (probability score less than or equal to 0.15).
Thus, 11 (85%) of the 13 mutation cases were categorised as luminal A. Three GS scores were calculated for each sample at baseline.
Owing to the small number of mutations found, GC were categorised as ' KRAS wild-type' or ' KRAS mutant' for statistical analyses.
Patients were categorised into established mutation groups according to their genotype with the less severe mutation determining the group (9).
When all patients were categorised based on BRCA mutation status, 48% (27 out of 56) of patients with a BRCA mutation had a history HSR compared with 6% (2 out of 31) in those without a BRCA mutation (P<0.0001).
Four of these horses were categorised as having the MCOA-phenotype and were genotyped as being homozygous for the PMEL17 mutation.
People were categorised by the job they did.
They were categorised as children with specific language impairment (SLI).
Studies were categorised as either measurement, descriptive or intervention.
Responses were categorised, collapsed and described using frequencies and percentages.
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Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com