Searcharxiv⌕ Search

arXiv subjects

Krzysztof Bartoszek

Publications and source records attributed to Krzysztof Bartoszek.

At least 19 recordsLinked to original sources

Bayesian inference of mixed Gaussian phylogenetic models

Background: Continuous traits evolution of a group of taxa that are correlated through a phylogenetic tree is commonly modelled using parametric stochastic differential equations to represent deterministic change of trait through time, while incorporating noises that represent different unobservable evolutionary pressures. Often times, a heterogeneous Gaussian process that consists of multiple parametric sub-processes is often used when the observed data come from a very diverse set of taxa. In the maximum likelihood setting, challenges can be found when exploring the involved likelihood surface and when interpreting the uncertainty around the parameters. Results: We extend the methods to tackle inference problems for mixed Gaussian phylogenetic models (MGPMs) by implementing a Bayesian scheme that can take into account biologically relevant priors. The posterior inference method is based on the Population Monte Carlo (PMC) algorithm that are easily parallelized, and using an efficient algorithm to calculate the likelihood of phylogenetically correlated observations. A model evaluation method that is based on the proximity of the posterior predictive distribution to the observed data is also implemented. Simulation study is done to test the inference and evaluation capability of the method. Finally, we test our method on a real-world dataset. Conclusion: We implement the method in the R package bgphy, available at github.com/bayubeta/bgphy. Simulation study demonstrates that the method is able to infer parameters and evaluate models properly, while its implementation on the real-world dataset indicates that a carefully selected model of evolution based on naturally occurring classifications results in a better fit to the observed data.

q-bio.PE↗

Identifying clusters in Czekanowski's diagram

Visualizing data through Czekanowski's diagram has as its aim the illustration of the relationships between objects. Often, obvious clusters of observations are directly visible. However, it is not straightforward to precisely delineate these clusters. This paper presents the development of the package RMaCzek, which now includes features for cluster identification in Czekanowski diagrams.

stat.AP↗

Revisiting the Nowosiółka skull with RMaCzek

One of the first fully quantitative distance matrix visualization methods was proposed by Jan Czekanowski at the beginning of the previous century. Recently, a software package, RMaCzek, was made available that allows for producing such diagrams in R. Here we reanalyze the original data that Czekanowski used for introducing his method, and in the accompanying code show how the user can specify their own custom distance functions in the package.

stat.AP↗

Multivariate Aspects of Phylogenetic Comparative Methods

This thesis concerns multivariate phylogenetic comparative methods. We investigate two aspects of them. The first is the bias caused by measurement error in regression studies of comparative data. We calculate the formula for the bias and show how to correct for it. We also study whether it is always advantageous to correct for the bias as correction can increase the mean square error of the estimate. We propose a criterion, which depends on the observed data, that indicates whether it is beneficial to correct or not. Accompanying the results is an R program that offers the bias correction tool. The second topic is a multivariate model for trait evolution which is based on an Ornstein-Uhlenbeck type stochastic process, often used for studying trait adaptation, co-evolution, allometry or trade-offs. Alongside the description of the model and presentation of its most important features we present an R program estimating the model's parameters. To the best of our knowledge our program is the first program that allows for nearly all combinations of key model parameters providing the biologist with a flexible tool for studying multiple interacting traits in the Ornstein-Uhlenbeck framework. There are numerous packages available that include the Ornstein-Uhlenbeck process but their multivariate capabilities seem limited. [COMMENT: Please note that this abstract and thesis is from 2011]

q-bio.PE↗

Stochastic models in phylogenetic comparative methods: analytical properties and parameter estimation

Phylogenetic comparative methods are well established tools for using inter-species variation to analyse phenotypic evolution and adaptation. They are generally hampered, however, by predominantly univariate approaches and failure to include uncertainty and measurement error in the phylogeny as well as the measured traits. This thesis addresses all these three issues. First, by investigating the effects of correlated measurement errors on a phylogenetic regression. Second, by developing a multivariate Ornstein-Uhlenbeck model combined with a maximum-likelihood estimation package in R. This model allows, uniquely, a direct way of testing adaptive coevolution. Third, accounting for the often substantial phylogenetic uncertainty in comparative studies requires an explicit model for the tree. Based on recently developed conditioned branching processes, with Brownian and Ornstein-Uhlenbeck evolution on top, expected species similarities are derived, together with phylogenetic confidence intervals for the optimal trait value. Finally, inspired by these developments, the phylogenetic framework is illustrated by an exploration of questions concerning "time since hybridization", the distribution of which proves to be asymptotically exponential. [COMMENT: Please note that this abstract and thesis is from 2013]

q-bio.PE↗

Asymptotic dynamics of generalized Kantorovich operators

We characterize the family of continuous functions $f\in C([0,1])$ such that the iterates $\widehat{T}^{k}_{i} f$ converge uniformly on $[0,1]$, where $\widehat{T}_i$ is a generalized Kantorovich operator. This gives an affirmative answer to the problem raised in 2021 by Acu and Rasa.

math.PR↗

"Old Techniques for New Times": the RMaCzek package for producing Czekanowski's Diagrams

Inspired by the MaCzek Visual Basic program we provide an R package, RMaCzek, that produces Czekanowski's diagram. Our package permits any seriation and distance method the user provides. In this paper we focus on the OLO and QAP_2SUM methods from the seriation package. We illustrate the possibilities of our package with three anthropological studies, one socio-economical one and a phylogenetically motivated simulation study.

stat.AP↗

Normal approximation for mixtures of normal distributions and the evolution of phenotypic traits

An explicit bound is given for the Kolmogorov distance between a mixture of normal distributions and a normal distribution with properly chosen parameter values. A random variable X has a mixture of normal distributions if its conditional distribution given some sigma-algebra is normal. The bound depends only on the first two moments of the first two conditional moments of X given this sigma-algebra. As an application, the Yule-Ornstein-Uhlenbeck model, used in the field of phylogenetic comparative methods, is considered. A bound is derived for the Kolmogorov distance between the distribution of the average value of a phenotypic trait over n related species and a normal distribution. The bound goes to 0 as n goes to infinity, extending earlier limit theorems by Bartoszek and Sagitov.

math.PR↗

Are official confirmed cases and fatalities counts good enough to study the COVID-19 pandemic dynamics? A critical assessment through the case of Italy

As the COVID-19 outbreak is developing the two most frequently reported statistics seem to be the raw confirmed case and case fatalities counts. Focusing on Italy, one of the hardest hit countries, we look at how these two values could be put in perspective to reflect the dynamics of the virus spread. In particular, we find that merely considering the confirmed case counts would be very misleading. The number of daily tests grows, while the daily fraction of confirmed cases to total tests has a change point. It (depending on region) generally increases with strong fluctuations till (around, depending on region) 15th-22nd March and then decreases linearly after. Combined with the increasing trend of daily performed tests, the raw confirmed case counts are not representative of the situation and are confounded with the sampling effort. This we observe when regressing on time the logged fraction of positive tests and for comparison the logged raw confirmed count. Hence, calibrating model parameters for this virus's dynamics should not be done based only on confirmed case counts (without rescaling by the number of tests), but take also fatalities and hospitalization count under consideration as variables not prone to be distorted by testing efforts. Furthermore, reporting statistics on the national level does not say much about the dynamics of the disease, which are taking place at the regional level. These findings are based on the official data of total death counts up to 15th April 2020 released by ISTAT and up to 10th May 2020 for the number of cases. In this work we do not fit models but we rather investigate whether this task is possible at all. This work also informs about a new tool to collect and harmonize official statistics coming from different sources in the form of a package for the R statistical environment and presents the COVID-19 Data Hub.

stat.AP↗

A Central Limit Theorem for Punctuated Equilibrium

Current evolutionary biology models usually assume that a phenotype undergoes gradual change. This is in stark contrast to biological intuition, which indicates that change can also be punctuated-the phenotype can jump. Such a jump could especially occur at speciation, i.e. dramatic change occurs that drives the species apart. Here we derive a Central Limit Theorem for punctuated equilibrium. We show that, if adaptation is fast, for weak convergence to normality to hold, the variability in the occurrence of change has to disappear with time.

q-bio.PE↗

Simulating an infinite mean waiting time

We consider a hybrid method to simulate the return time to the initial state in a critical-case birth--death process. The expected value of this return time is infinite, but its distribution asymptotically follows a power-law. Hence, the simulation approach is to directly simulate the process, unless the simulated time exceeds some threshold and if it does, draw the return time from the tail of the power law.

stat.ME↗

Limit distribution of the quartet balance index for Aldous's b>=0-model

This paper builds up on T. Martinez-Coronado, A. Mir, F. Rossello and G. Valiente's work "A balance index for phylogenetic trees based on quartets", introducing a new balance index for trees. We show here that this balance index, in the case of Aldous's b>=0-model, convergences weakly to a distribution that can be characterized as the fixed point of a contraction operator on a class of distributions.

q-bio.PE↗

Modelling trait dependent speciation with Approximate Bayesian Computation

Phylogeny is the field of modelling the temporal discrete dynamics of speciation. Complex models can nowadays be studied using the Approximate Bayesian Computation approach which avoids likelihood calculations. The field's progression is hampered by the lack of robust software to estimate the numerous parameters of the speciation process. In this work we present an R package, pcmabc, based on Approximate Bayesian Computations, that implements three novel phylogenetic algorithms for trait-dependent speciation modelling. Our phylogenetic comparative methodology takes into account both the simulated traits and phylogeny, attempting to estimate the parameters of the processes generating the phenotype and the trait. The user is not restricted to a predefined set of models and can specify a variety of evolutionary and branching models. We illustrate the software with a simulation-reestimation study focused around the branching Ornstein-Uhlenbeck process, where the branching rate depends non-linearly on the value of the driving Ornstein-Uhlenbeck process. Included in this work is a tutorial on how to use the software.

q-bio.PE↗

PSICA: decision trees for probabilistic subgroup identification with categorical treatments

Personalized medicine aims at identifying best treatments for a patient with given characteristics. It has been shown in the literature that these methods can lead to great improvements in medicine compared to traditional methods prescribing the same treatment to all patients. Subgroup identification is a branch of personalized medicine which aims at finding subgroups of the patients with similar characteristics for which some of the investigated treatments have a better effect than the other treatments. A number of approaches based on decision trees has been proposed to identify such subgroups, but most of them focus on the two-arm trials (control/treatment) while a few methods consider quantitative treatments (defined by the dose). However, no subgroup identification method exists that can predict the best treatments in a scenario with a categorical set of treatments. We propose a novel method for subgroup identification in categorical treatment scenarios. This method outputs a decision tree showing the probabilities of a given treatment being the best for a given group of patients as well as labels showing the possible best treatments. The method is implemented in an R package \textbf{psica} available at CRAN. In addition to numerical simulations based on artificial data, we present an analysis of a community-based nutrition intervention trial that justifies the validity of our method.

stat.ML↗

Fast likelihood evaluation for multivariate phylogenetic comparative methods: the PCMBase R package

We introduce an R package, PCMBase, to rapidly calculate the likelihood for multivariate phylogenetic comparative methods. The package is not specific to particular models but offers the user the functionality to very easily implement a wide range of models where the transition along a branch is multivariate normal. We demonstrate the package's possibilities on the now standard, multitrait Ornstein-Uhlenbeck process as well as the novel multivariate punctuated equilibrium model. The package can handle trees of various types (e.g. ultrametric, nonultrametric, polytomies, e.t.c.), as well as measurement error, missing measurements or non-existing traits for some of the species in the tree.

q-bio.PE↗

The phylogenetic effective sample size and jumps

The phylogenetic effective sample size is a parameter that has as its goal the quantification of the amount of independent signal in a phylogenetically correlated sample. It was studied for Brownian motion and Ornstein-Uhlenbeck models of trait evolution. Here, we study this composite parameter when the trait is allowed to jump at speciation points of the phylogeny. Our numerical study indicates that there is a non-trivial limit as the effect of jumps grows. The limit depends on the value of the drift parameter of the Ornstein-Uhlenbeck process.

q-bio.PE↗