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David C Tank

Publications and source records attributed to David C Tank.

2 recordsLinked to original sources

A targeted subgenomic approach for phylogenomics based on microfluidic PCR and high throughput sequencing

Advances in high-throughput sequencing (HTS) have allowed researchers to obtain large amounts of biological sequence information at speeds and costs unimaginable only a decade ago. Phylogenetics, and the study of evolution in general, is quickly migrating towards using HTS to generate larger and more complex molecular datasets. In this paper, we present a method that utilizes microfluidic PCR and HTS to generate large amounts of sequence data suitable for phylogenetic analyses. The approach uses a Fluidigm microfluidic PCR array and two sets of PCR primers to simultaneously amplify 48 target regions across 48 samples, incorporating sample-specific barcodes and HTS adapters (2,304 unique amplicons per microfluidic array). The final product is a pooled set of amplicons ready to be sequenced, and thus, there is no need to construct separate, costly genomic libraries for each sample. Further, we present a bioinformatics pipeline to process the raw HTS reads to either generate consensus sequences (with or without ambiguities) for every locus in every sample or--more importantly--recover the separate alleles from heterozygous target regions in each sample. This is important because it adds allelic information that is well suited for coalescent-based phylogenetic analyses that are becoming very common in conservation and evolutionary biology. To test our subgenomic method and bioinformatics pipeline, we sequenced 576 samples across 96 target regions belonging to the South American clade of the genus Bartsia L. in the plant family Orobanchaceae. After sequencing cleanup and alignment, the experiment resulted in [~]25,300bp across 486 samples for a set of 48 primer pairs targeting the plastome, and [~]13,500bp for 363 samples for a set of primers targeting regions in the nuclear genome. Finally, we constructed a combined concatenated matrix from all 96 primer combinations, resulting in a combined aligned length of [~]40,500bp for 349 samples.

Evolutionary Biology

Shifts in diversification rates linked to biogeographic movement into new areas, an example of disparate continental distributions and a recent radiation in the Andes

AcknowledgementsWe would like to thank S. Mathews for kindly sharing genomic DNA for some taxa used in this study. J. Sullivan, L. Harmon, E. Roalson, J. Beaulieu, B. Moore, N. Nurk, M. Pennell, T. Peterson, and two anonymous reviewers for helpful suggestions or comments on the manuscript. J. Beaulieu, L. Harmon, C. Blair and the University of Idaho Institute for Bioinformatics and Evolutionary Studies (NIH/NCRR P20RR16448 and P20RR016454) for computational aid. Funding for this work was provided by NSF DEB-1210895 to DCT for SUC, NSF DEB-1253463 to DCT, and Graduate Student Research Grants to SUC from the Botanical Society of America (BSA), the Society of Systematic Biologists (SSB), the American Society of Plant Taxonomists (ASPT), and the University of Idaho Stillinger Herbarium Expedition Funds.\n\nPremise of the studyClade specific bursts in diversification are often associated with the evolution of key innovations. However, in groups with no obvious morphological innovations, observed upticks in diversification rates have also been attributed to the colonization of a new geographic environment. In this study, we explore the systematics, diversification dynamics, and historical biogeography of the plant clade Rhinantheae in the Orobanchaceae, with a special focus on the Andean clade of the genus Bartsia L..\n\nMethodsWe sampled taxa from across Rhinantheae, including a representative sample of Andean Bartsia species. Using standard phylogenetic methods, we reconstructed evolutionary relationships, inferred divergence times among the clades of Rhinantheae, elucidated their biogeographic history, and investigated diversification dynamics.\n\nKey resultsWe confirmed that the South American Bartsia species form a highly supported monophyletic group. The median crown age of Rhinantheae was determined to be ca. 30 Ma, and Europe played an important role in the biogeographic history of the lineages. South America was first reconstructed in the biogeographic analyses around 9 Ma, and with a median age of 2.59 Ma, this clade shows a significant uptick in diversification.\n\nConclusionsIncreased net diversification of the South American clade corresponds with biogeographic movement into the New World. This happened at a time when the Andes were reaching the necessary elevation to host an alpine environment. Although a specific route could not be identified with certainty, we provide plausible hypotheses to how the group colonized the New World.

Evolutionary Biology