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Y chromosome haplogroup frequency distribution in controls from each of the four study populations from phase I was summarized and compared in Fig. 1b.
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Also, in that particular paragraph that lacks my own opinion, I was not sure how I was going to remove some of the in-text citations because [Researcher] said that those citations made that I was summarizing others' opinions as my opinion.
The results for Situation I are summarized in Table 6.
The values used for the parameters in the flow relations (k L,i a, c i, H i, p tot, r i ) are summarized in Table 2.
The design algorithm at node i is summarized as follows and is iteratively executed over all sensor nodes i = 1,…,M.
The results reveal that well-aligned ZNAs are also obviously formed for samples G, H, and I. Also, the mean values of the nanowire dimension and array density for samples G, H, and I are summarized in Table2.
where measurement matrix H is H = − 2 × ( p 1 − p 2 ) ⋯ ( p j − p k ) ⋯ ( p A − 1 − p A ) T. and measurement vector z i is z i = d ̂ i 1 2 − d ̂ i 2 2 − ∥ p 1 ∥ 2 + ∥ p 2 ∥ 2 ⋮ d ̂ ij 2 − d ̂ ik 2 − ∥ p j ∥ 2 + ∥ p k ∥ 2 ⋮ d ̂ iA − 1 2 − d ̂ iA 2 − ∥ p A − 1 ∥ 2 + ∥ p A ∥ 2. The proposed algorithm running on each normal node i is summarized in Algorithm 1.
The clinicopathological features for Cohorts I-III are summarized in Table 1.
In the second step, the univariable associations from the literature (L) and data at hand (I) are summarized.
The basic nodule information and their responses to CDDP-HAI are summarized in Tables 1 and 2, respectively.
The computational predictions for several mechanistic contributions to singlet relaxation in C2- I are summarized in Figure 3, which also shows a comparison with experiment.
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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