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After the 2DSA processes the noise measured from test vehicles during wide-open-throttle operation, dominant annoying transmission noise components can be extracted, and their sources can be identified through comparing feature orders obtained from geometric analysis.
Sex-biased genes are generally identified through comparing male and female samples.
Next, differentially expressed transcripts were identified through comparing gene expression profiles of each sampled tissue to the others.
The targets were identified through comparing the phenotypic fraction value, fPH (the ratio of weighted and dimensionless specific growth rate and specific isobutanol production rate) [ 12, 23, 24].
Genes specifically expressed during the incompatible interaction were identified through comparing the transcription profiling in the present study with that of our previous study on compatible interaction [ 34].
A total of 3,573,824 SNPs and 404,090 indels (of length ≤50 bp) were identified through comparing KWP1 genome with human reference genome (hg19) [ 17].
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After normalisation, differentially expressed genes with statistical significance were identified through two compared groups (t-test, P<0.05).
These genes have been identified through case/control association studies, comparing severe malaria to uncomplicated malaria cases.
Finally, categories of research topical areas identified through content analysis were compared against the small existing literature on CTP for health and nutrition in humanitarian and stable settings.
Harm identified through PTT screening was compared to harm identified through voluntary incidence reports in the department.
Dependability and confirmability were ascertained by the analysis process: a second investigator checked the reliability of coding; final themes were identified through consensus and were compared to original data in order to verify if they reflected an accurate representation of the participants' experiences of the intervention.
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