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Study design: In the present study, we used two well-established sets of PCR primers in different combinations for the detection of HPV DNA in 106 non-invasive brush biopsy samples of the oral mucosa and 56 samples from the cervix uteri.
Although some studies have appeared that use yellow and red fluorescent proteins for FRET studies [17] [20] a detailed side-by-side comparison of several combinations for the detection of FRET in single living cells is still lacking.
Thus, with a large number of SNPs and a wide range of configurations, this dataset is likely to provide informative SNP pair combinations for the detection of linked loci and the estimation of recombination fractions (Hackett et al. 2013; Li et al. 2014).
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Figure 8 Performance of each feature combination for the detection of gender, age range, and nationality.
The methylation markers CADM1 and MAL were found to be an optimal combination for the detection of CIN3 lesions [ 69].
The accuracy of this methylation combination for the detection of CIN3+ lesions in the triage of HR-HPV-positive women was 0.72.
However, the most specific and sensitive antigen or antigen combination for the detection of previous Campylobacter infection in a particular post-infectious sequel remains unknown.
Sensitivities, specificities, false-positive and false-negative results of CT, US abdomen, EUS, US neck, and chest X-ray, alone or in combination, for the detection of metastases in the various organs were calculated.
In the duplex, real-time PCR experiment, a UPL primer-probe (Universal Probe Library, Roche Diagnostics Ltd., UK) combination for the detection of the target gene, GRM7 (Supplementary Table SIV) and the TaqMan® RNase P CNR assay for the detection of a reference gene, RNase P was used.
Fig. 2 Categories of mapping populations and cross combinations used for the detection of representative rice QTLs. a Percentage of total articles using each type of mapping population.
We found that combining the method proposed by Audic and Claverie with Fisher's exact test and a method based on calculating the difference in relative frequency was the best combination for maximizing the detection of up-regulated genes.
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