2010
DOI: 10.1111/j.1755-0998.2009.02768.x
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DnaSAM: Software to perform neutrality testing for large datasets with complex null models

Abstract: Patterns of DNA sequence polymorphisms can be used to understand the processes of demography and adaptation within natural populations. High-throughput generation of DNA sequence data has historically been the bottleneck with respect to data processing and experimental inference. Advances in marker technologies have largely solved this problem. Currently, the limiting step is computational, with most molecular population genetic software allowing a gene-by-gene analysis through a graphical user interface. An e… Show more

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Cited by 23 publications
(31 citation statements)
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“…Haplotype analysis was performed as described in Campoli et al (2013). Nucleotide diversity π was calculated for the coding region using DnaSAM v. 20100621 (Eckert et al 2010). …”
Section: Methodsmentioning
confidence: 99%
“…Haplotype analysis was performed as described in Campoli et al (2013). Nucleotide diversity π was calculated for the coding region using DnaSAM v. 20100621 (Eckert et al 2010). …”
Section: Methodsmentioning
confidence: 99%
“…Significance of all tests was determined in DnaSAM [73] using 10 3 simulations that assumed a neutral model and no recombination. Because D , H , and EW differ in their sensitivities to demographic history, background selection, and recombination, the DHEW compound test [32] was also performed using the Perl script provided with DnaSAM [73].…”
Section: Methodsmentioning
confidence: 99%
“…Genomic windows along the linkage map were defined in 5-cM bins with a step size of 2 cM. All calculations were conducted using DnaSAM (Eckert et al 2010c) and the libsequence, analysis, and gestimator C++ libraries (Thornton 2003). The latter C++ library uses the method of Comeron (1995) to calculate nonsynonymous (K a ) and synonymous (K s ) divergences, with the average across pairwise comparisons between ingroup and outgroup sequences being presented for each statistic when multiple sequences were available from the outgroup.…”
Section: Discussionmentioning
confidence: 99%