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In order to further examine this pattern, we plotted the standardized residual error for this comparison by the calendar year of the observation (Fig. 3).
To investigate whether TF genes in nematodes exhibit a similar pattern, we plotted the physical locations of C. elegans and C. briggsae TF genes using non-overlapping windows of 200 kb (the genome of C. remanei has not yet been assembled and therefore was not used in this analysis).
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In order to examine whether the movements converged towards the model pattern through practice, we plotted the discriminant scores against the number of successfully mouth-opened (completely closed) canisters (Figure 3).
To examine across-tissue expression patterns, we plotted the across-tissue means and standard deviations of segments with three or more genes.
Not only did these rates differ, they formed a distinct pattern when we plotted the short-term rates of genetic gain against short-term rates of inbreeding for each restriction and overlaid this plot with the short-term response frontier for unrestricted OCS.
To further elucidate the collaboration patterns of neuroscientists, we plotted the histograms of the number of co-authors for abstracts and the number of abstracts submitted by authors.
To characterize differences in growth patterns through ontogeny, we plotted tail height against SVL.
To assess genomic patterns of LD, we plotted LD for all SNPs separated by 1−10 kbp by genomic location.
Because the time series is long, we plotted seasonal patterns once every five years, and also for the last year 20022).
To explore whether specific sequence patterns existed near the breaks, we plotted sequence logos of 1,080 reads (see the Sequence logo section in the Methods section).
In order to test whether OPTmorph1 and OPTmorph2 are useful discriminators of diel activity patterns in teleost reef fish we plotted the numerators (LD^2; PDmin^2) against the common denominator (ED × AL).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com