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Biology subjects

Lazarev, D.

Publications and source records attributed to Lazarev, D..

2 recordsLinked to original sources

Constrained Diffusion as a Paradigm for Evolution

A foundational question in computational biology is how to utilize data to describe the forces driving evolution. Here, we view evolution as a novel diffusion process constrained by many biological, physical, and environmental factors affecting organism viability at any given time. We introduce DiffEvol, a framework that models evolution as constrained diffusion over a discrete genotype space. Using real-world genomic sequence data alone, DiffEvol estimates complex evolutionary constraints by inverting the diffusion dynamics to recover a constrained subspace representing the viable genotype manifold, as well as its evolution over time. Applied to SARS-CoV-2 sequence data from 2020-2024, DiffEvol reconstructs constraint functions that recapitulate known viral fitness trends, including a pronounced "phase transition" that occurred following the widespread adoption of the SARS-CoV-2 vaccine. Our constraint subspace representation of the data characterizes such features and trends more clearly. This framework could be used not only to improve forecasting of emergent pathogenic strains, but also to produce more accurate reverse time analyses of their evolutionary dynamics to help identify ancestral variants and the forces having shaped a pathogens evolutionary trajectory. More generally, this formulation provides a method for linking observed sequence mutations to an evolving fitness landscape. Thus, constrained subspace diffusion offers a mathematical language for evolutionary dynamics in any system where random variation interacts with slowly-changing structural or global constraints, and can be applied to more complex evolutionary phenomena such as vaccine resistance, viral escape, and protein evolution.

bioinformatics↗

GUIDE deconstructs genetic architectures using association studies

Genome-wide association studies have revealed that the genetic architecture of most complex traits is characterized by a large number of distinct effects scattered across the genome. Functional enrichment analyses help provide some biological interpretation of associated variants but more work is needed to further translate GWAS hits into meaningful biological insights. Thus, we set out to leverage the genetic association results from many traits with a view to identifying the set of modules, or latent factors, that mediate these associations. The identification of such modules may aid in disease classification as well as the elucidation of complex disease mechanisms. We propose a method, Genetic Unmixing by Independent Decomposition (GUIDE), to estimate a set of statistically independent latent factors that best express the patterns of association across many traits. The resulting latent factors not only have desirable mathematical properties, such as sparsity and a higher variance explained for the latent factors that are significantly associated with a given trait, but are also able to single out and prioritize key biological features or pathophysiological mechanisms underlying a given trait or disease. Moreover, we show that these latent factors can isolate biological pathways as well as epidemiological and environmental influences that compose the genetic architecture of complex traits.

genetics↗