Search bioRxiv⌕ Search

Biology subjects

Sverdlov, S.

Publications and source records attributed to Sverdlov, S..

2 recordsLinked to original sources

The Epistasis Boundary: Linear vs. Nonlinear Genotype-Phenotype Relationships

Nonlinearity in the genotype-phenotype relationship can take the form of dominance, epistasis, or gene-environment interaction. The importance of nonlinearity, especially epistasis, in real complex traits is controversial. Network models in systems biology are typically highly nonlinear, yet the predictive power of linear quantitative genetic models is rarely improved by addition of nonlinear terms, and association studies detect few strong gene-gene interactions. We find that complex traits satisfying certain conditions can be well represented by a linear genetic model on an appropriate scale despite underlying biological complexity. Recent mathematical results in separability theory determine these conditions, which correspond to three biological criteria (Directional Consistency, Environmental Compensability, and Pathway Redundancy) together making up an Epistatic Boundary between systems suitable and unsuitable for linear modeling. For nonlinear traits, we introduce a classification of types of nonlinearity from a systems perspective, and use this to illustrate how upstream controlling genes, potentially more important to explaining biological function, can be intrinsically harder to detect by GWAS than their downstream controlled counterparts.

genomics↗

An Experiment in Learning the Language of Sequence Motifs: Sequence Logos vs. Finite-State Machines

Position weight matrices (PWMs) are the standard way to model binding site affinities in bioinformatics. However, they assume that symbol occurrences are position independent and, hence, they do not take into account symbols co-occurrence at different sequence positions. To address this problem, we propose to construct finite-state machines (FSMs) instead. A modified version of the Evidence-Driven State Merging (EDSM) heuristic is used to reduce the number of states as FSMs grow too quickly as a function of the number of sequences to reveal any useful structure. We tested our approach on sequence data for the transcription factor HNF4 and found out that the constructed FSMs provide small representations and an intuitive visualization. Furthermore, the FSM was better than PWMs at discriminating the positive and negative sequences in our data set.

bioinformatics↗