Exact(60)
Qualitative data are typically analyzed by either a deductive or an inductive method.
Twenty-two intubulopapillaryopapillary neoplasms were analyzed by either targeted next-generation sequencing, which enabled the identification of sequence mutations, copy number alterations, and selected structural rearrangements involving all targeted (≥300) genes, or whole-exome sequencing.
Continuing with the overall trend of higher drift times based on larger mass, ferulate ([M-H]-m/z 193.0501), the 3-O-methylated derivative of caffeate, and its saturated derivative, dihydroferulate ([M-H]-m/z 195.0657), displayed the best separation among the hydroxycinnamate pairs (see Figure 3) when analyzed by either UPLC-MS or UPLC-IMS, with drift times of 2.14 ms and 2.34 ms, respectively.
After 21 days, cells were analyzed by either von Kossa or Alizarin red staining.
Data were analyzed by either a Student's t-test or ANOVA using the R.2.6.1 software (http://www.r-project.org).org
The preparations were analyzed by either epifluorescence microscopy (Zeiss Axioplan 2) or by confocal laser microscopy (Leica TCS SP1).
To examine non-specific reactivity, all samples were analyzed by either omitting the primary antibody or by replacing the primary antibody with an isotype-matching antibody.
Protein expression was analyzed by either Coomassie, silver stain, or immunoblot techniques following 2D BN-PAGE, 2D SDS-PAGE and 3D SDS-PAGE.
Results were analyzed by either Student t test or ANOVA followed by Tukey test for comparisons between different groups, using InStat3 (GraphPad Software Inc., San Diego, CA).
Data are expressed as means ± SEM and were analyzed by either paired or unpaired two-tailed Student's t-test depending on sample collection.
Individual treatments were analyzed by either one-way ANOVA with Tukey's multiple comparisons post-test or two-tailed unpaired t-test.
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