SearcharxivSearch

arXiv subjects

Leo Lahti

Publications and source records attributed to Leo Lahti.

At least 19 recordsLinked to original sources

Memory reshapes stability landscapes: resilience-resistance tradeoffs and critical transitions

Regime shifts in biology, ecology, and other complex systems are often interpreted through stability landscapes and early warning signals that implicitly assume dynamics without memory effects. Yet many real systems exhibit these effects, thus present dynamics depend on past states and past forcing. Here, we study how memory reshapes bistable stability landscapes and regime shifts using a minimal bistable model with a fractional derivative that controls memory strength. We connect landscape geometry to classical notions of resilience and resistance by quantifying basin curvature and the perturbation magnitude required to cross the unstable threshold, and we track how these quantities evolve in time after perturbations. Memory typically flattens basin floors, slowing recovery, while often increasing the perturbation threshold for stability transitions, revealing a tradeoff between resilience and resistance. Because the landscape becomes history-dependent and time-evolving, memory generates qualitative behaviors that do not appear in memory-free models, including delayed collapse or recovery after stress ends, rebound after apparently successful transition, and broadened hysteresis under gradual parameter change. Finally, we show that fitting a memory-free model to memory-driven data can reproduce trajectories while systematically shifting equilibrium branches and tipping locations, risking incorrect diagnosis and management of regime shifts. These results motivate a moving landscape view and provide practical guidance for interpreting observed anomalies and distinguishing memory-driven effects from noise.

math.DS

DiPPER: A Bayesian approach to differential prevalence analysis with applications in microbiome studies

Recent evidence suggests that analyzing the presence/absence of taxonomic features can offer a compelling alternative to differential abundance analysis in microbiome studies. However, standard approaches to differential prevalence analysis face challenges with boundary cases and multiple testing. To address these limitations, we developed DiPPER (Differential Prevalence via Probabilistic Estimation in R), a method based on Bayesian hierarchical modeling. We benchmarked our method against existing differential prevalence methods, along with two differential abundance tools, using publicly available data from 57 human gut microbiome studies. We observed considerable variation in performance across the evaluated methods. Importantly, DiPPER demonstrated high sensitivity to detect potentially differentially prevalent features while maintaining a well-calibrated family-wise error rate under the global null hypothesis. Most notably, it outperformed the alternatives in the replication of findings across independent studies. Furthermore, DiPPER provides differential prevalence estimates and uncertainty intervals that are inherently adjusted for multiple testing.

stat.ME

Elementary methods provide more replicable results in microbial differential abundance analysis

Differential abundance analysis is a key component of microbiome studies. Although dozens of methods exist there is currently no consensus on the preferred methods. While the correctness of results in differential abundance analysis is an ambiguous concept and cannot be fully evaluated without setting the ground truth and employing simulated data, we argue that a well-performing method should be effective in producing highly reproducible results. We compared the performance of 14 differential abundance analysis methods by employing datasets from 53 taxonomic profiling studies based on 16S rRNA gene or shotgun metagenomic sequencing. For each method, we examined how the results replicated between random partitions of each dataset and between datasets from separate studies. While certain methods showed good consistency, some widely used methods were observed to produce a substantial number of conflicting findings. Overall, when considering consistency together with sensitivity, the best performance was attained by analyzing relative abundances with a non-parametric method (Wilcoxon test or ordinal regression model) or linear regression/t-test. Moreover, a comparable performance was obtained by analyzing presence/absence of taxa with logistic regression.

stat.AP

Learning and teaching biological data science in the Bioconductor community

Modern biological research is increasingly data-intensive, leading to a growing demand for effective training in biological data science. In this article, we provide an overview of key resources and best practices available within the Bioconductor project - an open-source software community focused on omics data analysis. This guide serves as a valuable reference for both learners and educators in the field.

cs.CY

Reconstructing ecological community dynamics from limited observations

Ecosystems tend to fluctuate around stable equilibria in response to internal dynamics and environmental factors. Occasionally, they enter an unstable tipping region and collapse into an alternative stable state. Our understanding of how ecological communities vary over time and respond to perturbations depends on our ability to quantify and predict these dynamics. However, the scarcity of long, dense time series data poses a severe bottleneck for characterising community dynamics using existing methods. We overcome this limitation by combining information across multiple short time series using Bayesian inference. By decomposing dynamics into deterministic and stochastic components using Gaussian process priors, we predict stable and tipping regions along the community landscape and quantify resilience while addressing uncertainty. After validation with simulated and real ecological time series, we use the model to question common assumptions underlying classical potential analysis and re-evaluate the stability of previously proposed "tipping elements" in the human gut microbiota.

stat.AP

Fractional modelling of COVID-19 transmission incorporating asymptomatic and super-spreader individuals

The COVID-19 pandemic has presented unprecedented challenges worldwide, necessitating effective modelling approaches to understand and control its transmission dynamics. In this study, we propose a novel approach that integrates asymptomatic and super-spreader individuals in a single compartmental model. We highlight the advantages of utilizing incommensurate fractional order derivatives in ordinary differential equations, including increased flexibility in capturing disease dynamics and refined memory effects in the transmission process. We conduct a qualitative analysis of our proposed model, which involves determining the basic reproduction number and analysing the disease-free equilibrium's stability. By fitting the proposed model with real data from Portugal and comparing it with existing models, we demonstrate that the incorporation of supplementary population classes and fractional derivatives significantly improves the model's goodness of fit. Sensitivity analysis further provides valuable insights for designing effective strategies to mitigate the spread of the virus.

q-bio.PE

iSEEtree: interactive explorer for hierarchical data

$\textbf{Motivation:}$ Hierarchical data structures are prevalent across several fields of research, as they represent an organised and efficient approach to study complex interconnected systems. Their significance is particularly evident in microbiome analysis, where microbial communities are classified at various taxonomic levels along the phylogenetic tree. In light of this trend, the R/Bioconductor community has established a reproducible analytical framework for hierarchical data, which relies on the highly generic and optimised TreeSummarizedExperiment data container. However, using this framework requires basic proficiency in programming. $\textbf{Results:}$ To reduce the entry requirements, we developed iSEEtree, an R shiny app which provides a visual interface for the analysis and exploration of TreeSummarizedExperiment objects, thereby expanding the interactive graphics capabilities of related work to hierarchical structures. This way, users can interactively explore several aspects of their data without the need for extensive knowledge of R programming. We describe how iSEEtree enables the exploration of hierarchical multi-table data and demonstrate its functionality with applications to microbiome analysis. $\textbf{Availability and Implementation:}$ iSEEtree was implemented in the R programming language and is available on Bioconductor at https://bioconductor.org/packages/iSEEtree under an Artistic 2.0 license. $\textbf{Contact:}$ giulio.benedetti@utu.fi or leo.lahti@utu.fi.

cs.MS

Epidemic Transmission Modeling with Fractional Derivatives and Environmental Pathogens

This research presents an advanced fractional-order compartmental model designed to delve into the complexities of COVID-19 transmission dynamics, specifically accounting for the influence of environmental pathogens on disease spread. By enhancing the classical compartmental framework, our model distinctively incorporates the effects of order derivatives and environmental shedding mechanisms on the basic reproduction numbers, thus offering a holistic perspective on transmission dynamics. Leveraging fractional calculus, the model adeptly captures the memory effect associated with disease spread, providing an authentic depiction of the virus's real-world propagation patterns. A thorough mathematical analysis confirming the existence, uniqueness, and stability of the model's solutions emphasizes its robustness. Furthermore, the numerical simulations, meticulously calibrated with real COVID-19 case data, affirm the model's capacity to emulate observed transmission trends, demonstrating the pivotal role of environmental transmission vectors in shaping public health strategies. The study highlights the critical role of environmental sanitation and targeted interventions in controlling the pandemic's spread, suggesting new insights for research and policy-making in infectious disease management.

q-bio.PE

FdeSolver: A Julia Package for Solving Fractional Differential Equations

Implementing and executing numerical algorithms to solve fractional differential equations has been less straightforward than using their integer-order counterparts, posing challenges for practitioners who wish to incorporate fractional calculus in applied case studies. Hence, we created an open-source Julia package, FdeSolver, that provides numerical solutions for fractional-order differential equations based on product-integration rules, predictor-corrector algorithms, and the Newton-Raphson method. The package covers solutions for one-dimensional equations with orders of positive real numbers. For high-dimensional systems, the orders of positive real numbers are limited to less than (and equal to) one. Incommensurate derivatives are allowed and defined in the Caputo sense. Here, we summarize the implementation for a representative class of problems, provide comparisons with available alternatives in Julia and Matlab, describe our adherence to good practices in open research software development, and demonstrate the practical performance of the methods in two applications; we show how to simulate microbial community dynamics and model the spread of Covid-19 by fitting the order of derivatives based on epidemiological observations. Overall, these results highlight the efficiency, reliability, and practicality of the FdeSolver Julia package.

math.NA

Probabilistic multivariate early warning signals

A broad range of natural and social systems from human microbiome to financial markets can go through critical transitions, where the system suddenly collapses to another stable configuration. Critical transitions can be unexpected, with potentially catastrophic consequences. Anticipating them early and accurately can facilitate controlled system manipulation and mitigation of undesired outcomes. Obtaining reliable predictions have been difficult, however, as often only a small fraction of the relevant variables can be monitored, and even minor perturbations can induce drastic changes in fragile states of a complex system. Data-driven indicators have been proposed as an alternative to prediction and signal an increasing risk of forthcoming transitions. Autocorrelation and variance are examples of generic indicators that tend to increase at the vicinity of an approaching tipping point across a range of systems. An important shortcoming in these and other widely studied indicators is that they deal with simplified one-dimensional representations of complex systems. Here, we demonstrate that a probabilistic data aggregation strategy can provide new ways to improve early warning detection by more efficiently utilizing the available information from multivariate time series. In particular, we consider a probabilistic variant of a vector autoregression model as a novel early warning indicator and argue that it has theoretical advantages related to model regularization, treatment of uncertainties, and parameter interpretation. We evaluate the performance against alternatives in a simulation benchmark and show improved sensitivity in EWS detection in a common ecological model encompassing multiple interacting species.

stat.AP

Three-species predator-prey model with respect to Caputo and Caputo-Fabrizio fractional operators

We study distributed lag effects in three-dimensional Lotka-Volterra systems by applying the concept of fractional calculus. We derive a new numerical method that provides enhanced stability for the Caputo-Fabrizio operator based on Adams-Bashforth method, considering non-singular kernel in the definition of Caputo-Fabrizio operator. We investigate the stability conditions of this system with comparisons to the Caputo fractional derivative. Numerical results show that the type of differential operators and the value of orders significantly influence the stability of the numerical solution, and dynamics of the Lotka-Volterra system.

math.NA

Linking statistical and ecological theory: Hubbell's unified neutral theory of biodiversity as a hierarchical Dirichlet process

Neutral models which assume ecological equivalence between species provide null models for community assembly. In Hubbell's Unified Neutral Theory of Biodiversity (UNTB), many local communities are connected to a single metacommunity through differing immigration rates. Our ability to fit the full multi-site UNTB has hitherto been limited by the lack of a computationally tractable and accurate algorithm. We show that a large class of neutral models with this mainland-island structure but differing local community dynamics converge in the large population limit to the hierarchical Dirichlet process. Using this approximation we developed an efficient Bayesian fitting strategy for the multi-site UNTB. We can also use this approach to distinguish between neutral local community assembly given a non-neutral metacommunity distribution and the full UNTB where the metacommunity too assembles neutrally. We applied this fitting strategy to both tropical trees and a data set comprising 570,851 sequences from 278 human gut microbiomes. The tropical tree data set was consistent with the UNTB but for the human gut neutrality was rejected at the whole community level. However, when we applied the algorithm to gut microbial species within the same taxon at different levels of taxonomic resolution, we found that species abundances within some genera were almost consistent with local community assembly. This was not true at higher taxonomic ranks. This suggests that the gut microbiota is more strongly niche constrained than macroscopic organisms, with different groups adopting different functional roles, but within those groups diversity may at least partially be maintained by neutrality.We also observed a negative correlation between body mass index and immigration rates within the family Ruminococcaceae.

q-bio.PE

Tipping Elements in the Human Intestinal Ecosystem

Recent studies show that the microbial communities inhabiting the human intestine can have profound impact on our well-being and health. However, we have limited understanding of the mechanisms that control this complex ecosystem. Based on a deep phylogenetic analysis of the intestinal microbiota in a thousand western adults we identified groups of bacteria that tend to be either nearly absent, or abundant in most individuals. The abundances of these bimodally distributed bacteria vary independently, and their contrasting alternative states are associated with host factors such as ageing and overweight. We propose that such bimodal groups represent independent tipping elements of the intestinal microbiota. These reflect the overall state of the intestinal ecosystem whose critical transitions can have profound health implications and diagnostic potential.

q-bio.QM

RPA: Probabilistic analysis of probe performance and robust summarization

Probe-level models have led to improved performance in microarray studies but the various sources of probe-level contamination are still poorly understood. Data-driven analysis of probe performance can be used to quantify the uncertainty in individual probes and to highlight the relative contribution of different noise sources. Improved understanding of the probe-level effects can lead to improved preprocessing techniques and microarray design. We have implemented probabilistic tools for probe performance analysis and summarization on short oligonucleotide arrays. In contrast to standard preprocessing approaches, the methods provide quantitative estimates of probe-specific noise and affinity terms and tools to investigate these parameters. Tools to incorporate prior information of the probes in the analysis are provided as well. Comparisons to known probe-level error sources and spike-in data sets validate the approach. Implementation is freely available in R/BioConductor: http://www.bioconductor.org/packages/release/bioc/html/RPA.html

cs.CE

Fully scalable online-preprocessing algorithm for short oligonucleotide microarray atlases

Accumulation of standardized data collections is opening up novel opportunities for holistic characterization of genome function. The limited scalability of current preprocessing techniques has, however, formed a bottleneck for full utilization of contemporary microarray collections. While short oligonucleotide arrays constitute a major source of genome-wide profiling data, scalable probe-level preprocessing algorithms have been available only for few measurement platforms based on pre-calculated model parameters from restricted reference training sets. To overcome these key limitations, we introduce a fully scalable online-learning algorithm that provides tools to process large microarray atlases including tens of thousands of arrays. Unlike the alternatives, the proposed algorithm scales up in linear time with respect to sample size and is readily applicable to all short oligonucleotide platforms. This is the only available preprocessing algorithm that can learn probe-level parameters based on sequential hyperparameter updates at small, consecutive batches of data, thus circumventing the extensive memory requirements of the standard approaches and opening up novel opportunities to take full advantage of contemporary microarray data collections. Moreover, using the most comprehensive data collections to estimate probe-level effects can assist in pinpointing individual probes affected by various biases and provide new tools to guide array design and quality control. The implementation is freely available in R/Bioconductor at http://www.bioconductor.org/packages/devel/bioc/html/RPA.html

q-bio.QM

Global modeling of transcriptional responses in interaction networks

Motivation: Cell-biological processes are regulated through a complex network of interactions between genes and their products. The processes, their activating conditions, and the associated transcriptional responses are often unknown. Organism-wide modeling of network activation can reveal unique and shared mechanisms between physiological conditions, and potentially as yet unknown processes. We introduce a novel approach for organism-wide discovery and analysis of transcriptional responses in interaction networks. The method searches for local, connected regions in a network that exhibit coordinated transcriptional response in a subset of conditions. Known interactions between genes are used to limit the search space and to guide the analysis. Validation on a human pathway network reveals physiologically coherent responses, functional relatedness between physiological conditions, and coordinated, context-specific regulation of the genes. Availability: Implementation is freely available in R and Matlab at http://netpro.r-forge.r-project.org

q-bio.MN

Cancer gene prioritization by integrative analysis of mRNA expression and DNA copy number data: a comparative review

A variety of genome-wide profiling techniques are available to probe complementary aspects of genome structure and function. Integrative analysis of heterogeneous data sources can reveal higher-level interactions that cannot be detected based on individual observations. A standard integration task in cancer studies is to identify altered genomic regions that induce changes in the expression of the associated genes based on joint analysis of genome-wide gene expression and copy number profiling measurements. In this review, we provide a comparison among various modeling procedures for integrating genome-wide profiling data of gene copy number and transcriptional alterations and highlight common approaches to genomic data integration. A transparent benchmarking procedure is introduced to quantitatively compare the cancer gene prioritization performance of the alternative methods. The benchmarking algorithms and data sets are available at http://intcomp.r-forge.r-project.org

cs.CE