2018
DOI: 10.1016/j.ympev.2018.09.001
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Phylogenetic analysis of Antarctic notothenioids illuminates the utility of RADseq for resolving Cenozoic adaptive radiations

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Cited by 77 publications
(92 citation statements)
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References 92 publications
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“…On average, this results in more polymorphic loci, that are each more informative. In a de novo context, these results will benefit any study focused on species with low diversity, and in particular phylogenetics studies, where sparse genotype matrices are being constructed across many species (Near et al, ). When RAD loci are ordered onto chromosomes (i.e., using a native reference genome, or if de novo‐assembled loci have been mapped to an external reference genome), a higher information density along the genome results, which should help resolve linkage patterns at a finer scale and identify evolutionary events that may have been missed with a sparser sampling of the genome (McKinney et al, ).…”
Section: Discussionmentioning
confidence: 98%
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“…On average, this results in more polymorphic loci, that are each more informative. In a de novo context, these results will benefit any study focused on species with low diversity, and in particular phylogenetics studies, where sparse genotype matrices are being constructed across many species (Near et al, ). When RAD loci are ordered onto chromosomes (i.e., using a native reference genome, or if de novo‐assembled loci have been mapped to an external reference genome), a higher information density along the genome results, which should help resolve linkage patterns at a finer scale and identify evolutionary events that may have been missed with a sparser sampling of the genome (McKinney et al, ).…”
Section: Discussionmentioning
confidence: 98%
“…The union of genome sampling protocols with massively parallel, short-read sequencing has produced an immensely successful research programme in population (Bassham, Catchen, Lescak, von Hippel, & Cresko, 2018), conservation (Dierickx, Shultz, Sato, Hiraoka, & Edwards, 2015) and landscape genomics (Bay et al, 2018), phylogenetics (Spriggs et al, 2019), and epigenetics (Trucchi et al, 2016), creating new experimental space for non-model organisms, and allowing, for example, ambitious sampling regimes in large geographical surveys (Dudaniec, Yong, Lancaster, Svensson, & Hansson, 2018), as well as wide-ranging taxon breadth in phylogenetic studies (Near et al, 2018). Regardless of the analytical approach, and in addition to any challenges of the experimental design, all RADseq strategies present two fundamental issues.…”
mentioning
confidence: 99%
“…A scenario of rapid cladogenesis-such as that hypothesised to have occurred during post-K-Pg extinction recovery -provides a logical explanation for the distinctive combination of extremely short phylogenetic internodes and incomplete lineage sorting that may be responsible for the lack of a clear branching pattern for this portion of the bird tree of life. The combination of a deep timescale and short times between phylogenetic divergences render this scenario among the most challenging of phylogenetic problems for molecular evidence to disentangle (Townsend et al 2012;Dornburg et al 2017aDornburg et al , 2017bDornburg et al , 2018. Additionally, expectations based on other rapid evolutionary radiations suggest the possibility of high levels of gene-flow among early diverging lineages (Meier et al 2017).…”
Section: Rapid Post-cretaceous Radiation As An Explanation For the 'Nmentioning
confidence: 99%
“…Advocates of this approach have long argued that investigators use predictive frameworks for selecting loci of high utility for specific phylogenetic problems (Townsend 2007;Townsend et al 2012;Chen et al 2015;Prum et al 2015;Dornburg et al 2016Dornburg et al , 2017bBleidorn 2017;Duchêne et al 2017a). The use and development of these approaches has largely been restricted to tackling issues arising when character states converge due to either substitution saturation (Dornburg et al 2014;Theriot et al 2015;Gilbert et al 2018;Near et al 2018) or biased patterns of nucleotide change (Borowiec et al 2015;Romiguier et al 2016;Dornburg et al 2017a). However, selecting loci that do not depict a signature of directional change in molecular rates as a consequence of life history shifts is also an experimental design problem.…”
Section: The Way Forwardmentioning
confidence: 99%
“…The genotyping-by-sequencing (GBS) technique can rapidly generate considerable numbers of genome-wide genetic markers, which has revolutionized the field of ecological and evolutionary genomics (Elshire et al, 2012;Andrews et al, 2016;Hume et al, 2018). Using the GBS technique, increasing numbers of studies have revealed fine-scale population genetic structure (Near et al, 2018;Palaiokostas et al, 2018;Robledo et al, 2018;Zhao et al, 2018). Most cryptic species have been distinguished by DNA-barcoding and other genetic methods, while few have been verified to be reproductively isolated or incompatible using interbreeding experiments (Kress et al, 2015;Lehnert et al, 2016;Paterson et al, 2016).…”
Section: Introductionmentioning
confidence: 99%