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Deep generative models in biological sequence and structure analysis and design.

Deep generative models have transformed biological sequence modeling from predictive analysis toward increasingly controllable design. Early biological applications of Variational Autoencoders (VAEs) and Generative Adversarial Networks (GANs) established latent representation learning and sequence synthesis, while recent advances in transformer-based language models, discrete diffusion, flow-matching, and multimodal generative frameworks have substantially expanded the scope of biological design. This review examines generative models for DNA, RNA, and protein sequence design, emphasizing how different model classes represent biological constraints, operate over discrete and continuous spaces, and integrate sequence, structure, and function. We compare VAEs, GANs, autoregressive and masked language models, diffusion models, and flow-based approaches across genomics, transcriptomics, and proteomics, with particular attention to controllability, long-range dependency modeling, structural grounding, generalization, and experimental utility. We further examine evaluation strategies, out-of-distribution generalization, and closed-loop design-build-test-learn workflows that connect in silico generation with empirical validation. We distinguish fundamental modality-dependent constraints including sequence discreteness, context length, structural coupling, and physical or thermodynamic requirements from architecture-dependent advantages that reflect the current state of the field. Current studies suggest that long-context models are particularly useful for genome-scale representation and sequence modeling, whereas structure-aware diffusion, flow-based, and inverse-folding approaches provide better frameworks for geometry-constrained RNA and protein design. This perspective provides a critical framework for understanding the present capabilities, limitations, and convergence of generative approaches toward reliable and experimentally grounded biological design.

Biological sequence analysis↗

Experiments with a universe for molecular modelling of biological processes.

A computer simulation program and results of preliminary simulations of an abstract two-dimensional universe are presented, in which biological and physical processes can be modelled at the molecular level. Two types of permanent elements (atoms) occupy squares of the universe: called 0 and 1. Atoms sharing a common square form a particle, with properties determined by its component atoms. Atoms, particles, and complexes of particles move and collide according to rules like those of classical mechanics. At a higher level of organization, the string of atoms in a particle is viewed as a program, whose execution can affect the space around the particle. The computer program (written in Turbo-Pascal language) can simulate the evolution of the universe starting from any given initial configuration of the particles. Three examples of simulations, showing the development of ordered spatial structures from initial sets of randomly distributed particles, illustrate the universe's potential in modelling various molecular processes.

Cell Wall↗

[Synthesis and characterization of model system in biological related function--model compounds for investigation of metal-metal interaction and nucleobase-aromatics interaction].

Several kinds of compounds available as model systems to investigation on metal-metal interaction in metalloproteins and on interaction of aromatics with nucleobases in arene intercalation to DNA were synthesized and characterized by spectrometry. Double and triple layered porphyrinophanes linked with 1,1'- or 1,3-disubstituted ferrocene moieties and their iron and cobalt complexes were prepared. Stabilities of their oxygenation complexes depended on bridging mode, lengths of alkyl linkers, distance between metals, and feature of hydrophobic cavity. Ferrocenophane derivatives in which nucleobase and aromatic hydrocarbon (naphthalene or anthracene) moieties substituted to their cyclopentadienyl rings in a stacking mode between the two chromophores were synthesized, as a model system of intercalation of aromatic condensed-ring hydrocarbons to DNA. Characterization of the ferrocenophanes by spectrometry and molecular modeling suggested that these chromophores interacted due to NH-pi hydrogen bonding and pi-pi charge transfer. A number of porphyrin derivatives covalently connected with a nucleobase or a nucleobase pair in a face-to-face mode between the porphyrin and nucleobase moiety were synthesized. The spectroscopic behavior of the derivatives indicate a greater affinity of the guanine-cytosine pair for porphyrin in comparison with the adenine-thymine pair. These results are compatible with the already reported spectroscopic and kinetic properties of mixing system of DNA and porphyrin derivatives. Moreover, the fluorescence spectra of the nucleobase-porphyrin derivatives gave a piece of evidence to cause DNA cleavage by photosensitizer via "type I" mechanism, in which direct action of singlet or triplet state of photosensitizer excited by laser irradiation brings about damage of cell or DNA.

DNA Damage↗

Spatial self-organization in a cyclic resource-species model.

Biological communities are remarkable in their ability to form cooperative ensembles that lead to coexistence through various types of niche partitioning, usually intimately tied to spatial structure. This is especially true in microbial settings where differential expression and regulation of genes allows members of a given species to alter their lifestyle so as to fill a functional role within the community. The resulting species interactions can involve feedback, as in the case of some bacterial consortia that participate in the cooperative degradation of a given resource in a succession of steps and in such a way that certain "later" species provide catalytic support for the primary degrader. We seek to capture the essential features of such spatially extended biological systems by introducing a lattice-based stochastic spatial model (interacting particle system) with cyclic local dynamics. Here, a given site progresses through a sequence of resource and species states in a prescribed order. Furthermore, this succession of states (at a site) is assumed to form a cyclic pattern due to a natural feedback mechanism. We explore conditions under which all the species are able to coexist and consider the extent to which this coexistence requires the development of spatio-temporal patterns, including spiral waves. This self-organization, if it occurs, results when synchronization of the dynamics at the microscopic level leads to macroscopic patterns. These patterns result in consumer-driven resource fluctuations that generate a form of spatio-temporal niche partitioning. As with most models of this complexity, we employ a mixture of mathematical analysis and simulations to develop an understanding of the resulting dynamics.

Adaptation, Biological↗

The modelling of biological systems in three dimensions using the time domain finite-difference method: I. The implementation of the model.

A computer method has been developed which uses the time domain finite-difference (TDFD) algorithm to calculate the deposition of the electromagnetic (EM) field in three-dimensional biological models. This, the first of two papers, describes the algorithm and the computer programs developed. The method is demonstrated by calculating the penetration of the EM field from a rectangular waveguide radiating into a homogeneous model, the calculation being carried out in two dimensions for simplicity in this paper.

Computer Simulation↗

Quantitative modeling and biology: the multivariate approach.

Even though elegant examples of mathematical modeling of biological problems exist, such approaches still remain outside the domain of most biologists. It is proposed that, for a wider and more systematic use of mathematical models in biology, the soft modeling approaches, which are applicable to phenomena with a limited level of definition, should be investigated and preferred. In particular, multivariate data analysis (MDA) is indicated as an important tool toward fulfilling this goal. This paper reviews the general principles of MDA and examines in detail principal component analysis and cluster analysis, which are two of the most important MDA techniques. A number of applications to real biological problems are presented. These examples show how the construction of classifications corresponds to the generation of new knowledge and new concepts, which are hierarchically on a higher level than the initial information. This new form of knowledge is obtained without superimposing a priori theories on the data. It is demonstrated how the MDA can lead to the identification of biological systems; also shown is their ability to describe multiple scale phenomena, a typical feature of biological systems. Moreover, the multivariate analyses provide new descriptors for a given biological system; these descriptors are quantitative, thus allowing the system to be described in a "metric space," where it then becomes possible to use any other mathematical tool.

Animals↗

Global positive coexistence of a nonlinear elliptic biological interacting model.

The purpose of this note is to give a necessary and sufficient condition for the coexistence of positive solutions to a rather general type of elliptic predator-prey system of the Dirichlet problem on the bounded domain omega when omega is a subset of Rn is large. The result is that the partial differential equation system possesses positive coexistence if and only if the corresponding ordinary differential equation system has positive equilibrium, the positive constant states. This result thus yields an algebraically computable criterion for the positive coexistence of predator and prey in many biological models.

Animals↗

"Dynamic" biological exposure indexes for n-hexane and 2,5-hexanedione, suggested by a physiologically based pharmacokinetic model.

Biological exposure index (BEI) of n-hexane was studied for accuracy using a physiologically based pharmacokinetic (PB-PK) model. The kinetics of n-hexane in alveolar air, blood, urine, and other tissues were simulated for different values of alveolar ventilations and also for constant and variable exposures. The kinetics of 2,5-hexanedione, the toxic n-hexane metabolite, were also simulated. The ranges of n-hexane concentrations in biological media and the urinary concentrations of 2,5-hexanedione are discussed in connection with a mean n-hexane exposure of 180 mg/m3 (50 ppm) (threshold limit value [TLV] suggested by American Conference of Governmental Industrial Hygienists [ACGIH] for 1988-89). The experimental and field data as well as those predicted by simulation with the PB-PK model were comparable. The physiological-pharmacokinetic simulations are used to propose the "dynamic" BEIs of n-hexane and 2,5-hexanedione. The use of simulation with PB-PK models enables a better understanding of the limits, advantages, and issues associated with biological monitoring of exposures to industrial solvents.

Hexanes↗

A new model for biological pattern formation.

Various non-equilibrium growth models have been used to explore the development of morphology in biological systems. Here we review a class of biological growth models which exhibit fractal structures and discuss the relationship of these models to a variety of other phenomena.

Diffusion↗

Advances in systems biology: measurement, modeling and representation.

Systems biology is frequently defined as the study of all of the elements in a biological system and their relationship to one another in response to perturbation. Advances in science and technology are enabling the development of this emerging and cross-disciplinary field by allowing researchers to explore how biological components function as a network in cells, tissues and organisms. Recently, pharmaceutical companies have begun to embrace systems approaches in an effort to better understand physiology, pathogenic processes and pharmacological responses. This review focuses on recent advances within three core areas of systems biology: data collection, data analysis, and the integration and sharing of data.

Animals↗

Causality in epidemiology.

Epidemiology represents an interesting and unique example of cross-fertilization between social and natural sciences. Epidemiology has evolved from a monocausal to a multicausal concept of the "web of causation", thus mimicking a similar and much earlier shift in the social sciences. However, in comparison with the social sciences epidemiology is both more sensitive to underlying biological models (which condition the interpretation of population findings), and more prone to a simplification of the causal pathways. Paradoxically, epidemiology has developed more sophisticated theoretical models for bias and confounding than the social sciences did, but for the practical purpose of identifying single preventable risk factors. Epidemiology makes use more often of study designs that simulate experimentation, than of surveys in the general population.

Bias↗

Models of intervention in menopause: proposal of a holistic or integral model.

OBJECTIVE: On the threshold of the third millennium, menopause has become a crucial social and health problem in developed countries. In the present work, we analyze possible healthcare strategies, describing their advantages and disadvantages within the context of different underlying conceptions of menopause. DESIGN: We have considered three theoretical frameworks or "menopause models": the biological model, the psychosocial model, and the holistic or integral model. Each model is examined under three subheadings: concept, contributions, and criticisms. RESULTS: The holistic model is proposed and defended as a valid option for the management of menopause. CONCLUSIONS: Adoption of the holistic model by health personnel may improve the attention given to menopausal women. As characteristics of such a model, the following are important: (1) The positive vision of the climacteric transition as an opportunity for personal growth, (2) the biopsychosocial perspective of the phenomena responsible for the different effects on the level of health and quality of life of women, (3) the development of health policies focused on health promotion, (4) the protagonism of women through strategies based on self-care and self-help groups, and (5) individualized use of hormone replacement therapy.

Aged↗

Solvable biological evolution model with a parallel mutation-selection scheme.

Based on the connection between a quantum spin model and an asexual biological evolution model with a single-peak fitness function in parallel mutation-selection scheme, we solve exactly both static and dynamics of the evolution model. We find that relaxation in such a parallel scheme is faster than that in a connected scheme of Eigen model. Our method can also be extended to other fitness functions.

Journal Article↗

Gene transfer to epidermal stem cells: implications for tissue engineering.

The skin is an attractive target for gene therapy because it is easily accessible and shows great potential as an ectopic site for protein delivery in vivo. Genetically modified epidermal cells can be used to engineer three-dimensional skin substitutes, which when transplanted can act as in vivo 'bioreactors' for delivery of therapeutic proteins locally or systemically. Although some gene transfer technologies have the potential to afford permanent genetic modification, differentiation and eventual loss of genetically modified cells from the epidermis results in temporary transgene expression. Therefore, to achieve stable long-term gene expression, it is critical to deliver genes to epidermal stem cells, which possess unlimited growth potential and self-renewal capacity. This review discusses the recent advances in epidermal stem cell isolation, gene transfer and engineering of skin substitutes. Recent efforts that employ gene therapy and tissue engineering for the treatment of genetic diseases, chronic wounds and systemic disorders, such as leptin deficiency or diabetes, are reviewed. Finally, the use of gene-modified tissue-engineered skin as a biological model for understanding tissue development, wound healing and epithelial carcinogenesis is also discussed.

Animals↗