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Dive into the research topics where Benjamin Kaehler is active.

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Featured researches published by Benjamin Kaehler.


Systematic Biology | 2015

Genetic Distance for a General Non-Stationary Markov Substitution Process

Benjamin Kaehler; Von Bing Yap; Rongli Zhang; Gavin A. Huttley

The genetic distance between biological sequences is a fundamental quantity in molecular evolution. It pertains to questions of rates of evolution, existence of a molecular clock, and phylogenetic inference. Under the class of continuous-time substitution models, the distance is commonly defined as the expected number of substitutions at any site in the sequence. We eschew the almost ubiquitous assumptions of evolution under stationarity and time-reversible conditions and extend the concept of the expected number of substitutions to nonstationary Markov models where the only remaining constraint is of time homogeneity between nodes in the tree. Our measure of genetic distance reduces to the standard formulation if the data in question are consistent with the stationarity assumption. We apply this general model to samples from across the tree of life to compare distances so obtained with those from the general time-reversible model, with and without rate heterogeneity across sites, and the paralinear distance, an empirical pairwise method explicitly designed to address nonstationarity. We discover that estimates from both variants of the general time-reversible model and the paralinear distance systematically overestimate genetic distance and departure from the molecular clock. The magnitude of the distance bias is proportional to departure from stationarity, which we demonstrate to be associated with longer edge lengths. The marked improvement in consistency between the general nonstationary Markov model and sequence alignments leads us to conclude that analyses of evolutionary rates and phylogenies will be substantively improved by application of this model.


Mbio | 2018

Optimizing taxonomic classification of marker-gene amplicon sequences with QIIME 2’s q2-feature-classifier plugin

Nicholas A. Bokulich; Benjamin Kaehler; Jai Ram Rideout; Matthew Dillon; Evan Bolyen; Rob Knight; Gavin A. Huttley; J. Gregory Caporaso

BackgroundTaxonomic classification of marker-gene sequences is an important step in microbiome analysis.ResultsWe present q2-feature-classifier (https://github.com/qiime2/q2-feature-classifier), a QIIME 2 plugin containing several novel machine-learning and alignment-based methods for taxonomy classification. We evaluated and optimized several commonly used classification methods implemented in QIIME 1 (RDP, BLAST, UCLUST, and SortMeRNA) and several new methods implemented in QIIME 2 (a scikit-learn naive Bayes machine-learning classifier, and alignment-based taxonomy consensus methods based on VSEARCH, and BLAST+) for classification of bacterial 16S rRNA and fungal ITS marker-gene amplicon sequence data. The naive-Bayes, BLAST+-based, and VSEARCH-based classifiers implemented in QIIME 2 meet or exceed the species-level accuracy of other commonly used methods designed for classification of marker gene sequences that were evaluated in this work. These evaluations, based on 19 mock communities and error-free sequence simulations, including classification of simulated “novel” marker-gene sequences, are available in our extensible benchmarking framework, tax-credit (https://github.com/caporaso-lab/tax-credit-data).ConclusionsOur results illustrate the importance of parameter tuning for optimizing classifier performance, and we make recommendations regarding parameter choices for these classifiers under a range of standard operating conditions. q2-feature-classifier and tax-credit are both free, open-source, BSD-licensed packages available on GitHub.


Insect Biochemistry and Molecular Biology | 2015

Folding behavior of four silks of giant honey bee reflects the evolutionary conservation of aculeate silk proteins.

Jakkrawut Maitip; Holly E. Trueman; Benjamin Kaehler; Gavin A. Huttley; Panuwan Chantawannakul; Tara D. Sutherland

Multiple gene duplication events in the precursor of the Aculeata (bees, ants, hornets) gave rise to four silk genes. Whilst these homologs encode proteins with similar amino acid composition and coiled coil structure, the retention of all four homologs implies they each are important. In this study we identified, produced and characterized the four silk proteins from Apis dorsata, the giant Asian honeybee. The proteins were readily purified, allowing us to investigate the folding behavior of solutions of individual proteins in comparison to mixtures of all four proteins at concentrations where they assemble into their native coiled coil structure. In contrast to solutions of any one protein type, solutions of a mixture of the four proteins formed coiled coils that were stable against dilution and detergent denaturation. The results are consistent with the formation of a heteromeric coiled coil protein complex. The mechanism of silk protein coiled coil formation and evolution is discussed in light of these results.


Journal of Theoretical Biology | 2017

Full reconstruction of non-stationary strand-symmetric models on rooted phylogenies

Benjamin Kaehler

Understanding the evolutionary relationship among species is of fundamental importance to the biological sciences. The location of the root in any phylogenetic tree is critical as it gives an order to evolutionary events. None of the popular models of nucleotide evolution currently used in likelihood or Bayesian methods are able to infer the location of the root without exogenous information. It is known that the most general Markov models of nucleotide substitution also cannot identify the location of the root or be fitted to multiple sequence alignments with fewer than three sequences. We prove that the location of the root and the full model can be identified and statistically consistently estimated for a non-stationary, strand-symmetric substitution model given a multiple sequence alignment with two or more sequences. We also generalise earlier work to provide a practical means of overcoming the computationally intractable problem of labelling hidden states in a phylogenetic model.


Genome Biology and Evolution | 2017

Standard Codon Substitution Models Overestimate Purifying Selection for Non-Stationary Data

Benjamin Kaehler; Von Bing Yap; Gavin A. Huttley

Estimation of natural selection on protein-coding sequences is a key comparative genomics approach for de novo prediction of lineage-specific adaptations. Selective pressure is measured on a per-gene basis by comparing the rate of non-synonymous substitutions to the rate of synonymous substitutions. All published codon substitution models have been time-reversible and thus assume that sequence composition does not change over time. We previously demonstrated that if time-reversible DNA substitution models are applied in the presence of changing sequence composition, the number of substitutions is systematically biased towards overestimation. We extend these findings to the case of codon substitution models and further demonstrate that the ratio of non-synonymous to synonymous rates of substitution tends to be underestimated over three data sets of mammals, vertebrates, and insects. Our basis for comparison is a non-stationary codon substitution model that allows sequence composition to change. Goodness-of-fit results demonstrate that our new model tends to fit the data better. Direct measurement of non-stationarity shows that bias in estimates of natural selection and genetic distance increases with the degree of violation of the stationarity assumption. Additionally, inferences drawn under time-reversible models are systematically affected by compositional divergence. As genomic sequences accumulate at an accelerating rate, the importance of accurate de novo estimation of natural selection increases. Our results establish that our new model provides a more robust perspective on this fundamental quantity.Estimation of natural selection on protein-coding sequences is a key comparative genomics approach for de novo prediction of lineage-specific adaptations. Selective pressure is measured on a per-gene basis by comparing the rate of nonsynonymous substitutions to the rate of synonymous substitutions. All published codon substitution models have been time-reversible and thus assume that sequence composition does not change over time. We previously demonstrated that if time-reversible DNA substitution models are applied in the presence of changing sequence composition, the number of substitutions is systematically biased towards overestimation. We extend these findings to the case of codon substitution models and further demonstrate that the ratio of nonsynonymous to synonymous rates of substitution tends to be underestimated over three data sets of mammals, vertebrates, and insects. Our basis for comparison is a nonstationary codon substitution model that allows sequence composition to change. Goodness-of-fit results demonstrate that our new model tends to fit the data better. Direct measurement of nonstationarity shows that bias in estimates of natural selection and genetic distance increases with the degree of violation of the stationarity assumption. Additionally, inferences drawn under time-reversible models are systematically affected by compositional divergence. As genomic sequences accumulate at an accelerating rate, the importance of accurate de novo estimation of natural selection increases. Our results establish that our new model provides a more robust perspective on this fundamental quantity.


bioRxiv | 2018

Species-level microbial sequence classification is improved by source-environment information

Benjamin Kaehler; Nicholas A. Bokulich; J. Gregory Caporaso; Gavin A. Huttley

Popular naive Bayes taxonomic classifiers for amplicon sequences assume that all species in the reference database are equally likely to be observed. We demonstrate that classification accuracy degrades linearly with the degree to which that assumption is violated, and in practice it is always violated. By incorporating environment-specific taxonomic abundance information, we demonstrate that species-level resolution is attainable.


PLOS ONE | 2018

Did aculeate silk evolve as an antifouling material

Tara D. Sutherland; Alagacone Sriskantha; Trevor D. Rapson; Benjamin Kaehler; Gavin A. Huttley

Many of the challenges we currently face as an advanced society have been solved in unique ways by biological systems. One such challenge is developing strategies to avoid microbial infection. Social aculeates (wasps, bees and ants) mitigate the risk of infection to their colonies using a wide range of adaptations and mechanisms. These adaptations and mechanisms are reliant on intricate social structures and are energetically costly for the colony. It seems likely that these species must have had alternative and simpler mechanisms in place to ensure the maintenance of hygienic domicile conditions prior to the evolution of these complex behaviours. Features of the aculeate coiled-coil silk proteins are reminiscent of those of naturally occurring α-helical antimicrobial peptides (AMPs). In this study, we demonstrate that peptides derived from the aculeate silk proteins have antimicrobial activity. We reconstruct the predicted ancestral silk sequences of an aculeate ancestor that pre-dates the evolution of sociality and demonstrate that these ancestral sequences also contained peptides with antimicrobial properties. It is possible that the silks evolved as an antifouling material and facilitated the evolution of sociality. These materials serve as model materials for consideration in future biomaterial development.


Journal of Social Structure | 2018

q2-sample-classifier: machine-learning tools for microbiome classification and regression

Nicholas A. Bokulich; Matthew Dillon; Evan Bolyen; Benjamin Kaehler; Gavin A. Huttley; J Caporaso

Summary q2-sample-classifier is a plugin for the QIIME 2 microbiome bioinformatics platform that facilitates access, reproducibility, and interpretation of supervised learning (SL) methods for a broad audience of non-bioinformatics specialists.


Mathematical Methods of Statistics | 2010

A Generalized Skewness Statistic for Stationary Ergodic Martingale Differences

Benjamin Kaehler; Ross Maller

We present a class of generalized skewness statistics depending on a parameter β > 0 and containing the usual skewness statistic when β = 3, but providing greater flexibility for modelling and testing skewness when β ≠ 3. The statistics’ suitability for financial applications is illustrated using a large data set from the Australian share market. Data is assumed to be observations on stationary ergodicmartingale differences with possibly leptokurtic marginals, rather than independent identically distributed samples. The statistics can be studentized for use in hypothesis testing. Proof is provided of their asymptotic distributions undermild assumptions. Rates of convergence and power of the tests against skewed alternatives are assessed using simulation.


Stochastic Processes and their Applications | 2017

Multivariate Subordination using Generalised Gamma Convolutions with Applications to V.G. Processes and Option Pricing

Boris Buchmann; Benjamin Kaehler; Ross Maller; Alexander Szimayer

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Gavin A. Huttley

Australian National University

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Rob Knight

University of California

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Ross Maller

Australian National University

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Tara D. Sutherland

Commonwealth Scientific and Industrial Research Organisation

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Von Bing Yap

National University of Singapore

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Alagacone Sriskantha

Commonwealth Scientific and Industrial Research Organisation

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Boris Buchmann

Australian National University

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Holly E. Trueman

Commonwealth Scientific and Industrial Research Organisation

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Trevor D. Rapson

Commonwealth Scientific and Industrial Research Organisation

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Rongli Zhang

National University of Singapore

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