Sentence examples for computing diversity from inspiring English sources

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We have unified social and natural sciences by showing that the above methods are applicable in both disciplines, at least if willing to take the trivial step of computing diversity as one minus segregation.

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DnaSP v.5 [25] was used to compute diversity indices, including nucleotide and haplotype diversity and the average number of nucleotide differences.

Using the same distance matrix, we computed diversity and haplotype connectivity scores for each of the 10 sampling locations as explained in the Methods section (using the measure AD for diversity).

It can be observed that both the measured and simulated correlation coefficients ρ are around 0.3 which are non-negligible in computing the diversity gain of the DAS. Figure 13 A symmetric environment where measurement was conducted.

We show that a simple reciprocal best hit method identified orthologs with sufficient reliability for the purposes of computing sequence diversity.

First, we subsampled only the 136 populations studied by Pemberton et al. (2013) from countries with geographic coordinates that placed them in the earlier set of 21 countries, repeating the same regressions, again computing observed diversity for a country by averaging values for its constituent populations.

However, one advantage of the approach of Caballero and Toro [ 11] is the fact that there is no need to give weight to within- and between-diversities to compute total diversity, since by definition GD T is the sum of GD WS and GD BS.

[30] compute diversity within selected instances from their conditional error.

Shannon diversity and Sørensen's similarity indices were used to compute species diversity and similarity, respectively, between field types and land-uses.

We used the PhiPack software, that also computes two diversity indices: The mean Pi values (i.e., the nucleotide diversity defined as the average number of nucleotide differences per site between any pair of DNA sequences randomly chosen from the sample) and the mean number of informative sites (IS) per alignment.

We computed nucleotide diversity for non-overlapping 10-kb and 100-kb windows along the Nipponbare RefSeq by adopting an approach similar to VariScan54 for genome-wide DNA polymorphism analyses and implemented as a custom R script.

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