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To confirm the alignment of the data sets, we compared locations in the MDS plot of individuals from the Native American, Latino, Jewish, Asian Indian, CGP, Pacific Islander, and African data sets with those of the HGDP-CEPH individuals.
Concerns about randomisation are a notable feature of Figure 1, a parallel coordinate plot of individuals' responses to the seven questions, divided for visual convenience into the four groups previously mentioned (based on replies to questions 3 and 7).
To further demonstrate that after merging, major systematic genotype differences did not exist between data sets of origin, we compared locations in the MDS plot of individuals from each data set to those of individuals in the worldwide HGDP-CEPH data set.
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Figure 5 Plot of individual PSNRs and average PSNR.
(A) Plot of individual differences between lung weights measured with balancepost-exsang.
Figure 1 shows a spaghetti plot of individual patients' FDG SUV for baseline and post-therapy for AI (Figure 1a) and T-treated (Figure 1b) groups undergoing approximately 2 weeks of targeted therapy.
This argument is further verified with other experiments Figure 2 Plot of individual PSNRs achieved by the co-opetition, NBS SP. User 1: Foreman (CIF, TL, 30 Hz), user 2: Mobile (CIF, 30 Hz).
A plot of individual membership coefficients for K = 19 reveals a high number of population clusters with average individual membership coefficients (i.e. posterior probabilities) greater than 0.9 (Figure 2, Table 2).
Figure 1a shows a box plot of individual study effect sizes obtained from Henry et al. [14]; the figure reveals, consistent with Henry et al.'s conclusions, that low demand conditions are associated with smaller effect sizes than high demand conditions.
Supplemental Fig. 1 Spaghetti plot of individual BTL trajectories.
Additional file 7: Figure S3 shows example matrix plot of individual replicate amplification for 1 pg.
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