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Frazer, S. A.

Publications and source records attributed to Frazer, S. A..

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Accessible and Robust Machine Learning Approaches to Improve the Opsin Genotype-Phenotype Map

Predicting phenotypes from genetic variation is a central challenge in biology. Linking genotypes and phenotypes using machine learning (ML) offers great promise, but its use is limited by poor accessibility, overestimated performance, and a "data-cliff"--a gap between abundant sequences and scarce functional measurements. To develop more robust methods for genotype-phenotype prediction, an outstanding model system is opsin genes, visual pigments with extensive phenotypic information that strongly influence animal spectral sensitivity. Here we advance ML characterization of the opsin genotype-phenotype map through four main contributions. First, we introduce the Opsin Phenotype Tool for Inference of Color Sensitivity (OPTICS), a user-friendly platform for predicting maximum wavelength sensitivity ({lambda}max) from amino-acid sequences. Second, we show that encoding sequences with amino-acid physicochemical properties improves predictive performance and reveals mechanistic relationships. Third, we develop Phylogenetically Weighted Cross-Validation (PW-CV), a method that accounts for non-independence among related sequences, providing more realistic assessments of model generalizability. Finally, we present the Mine-N-Match (MNM) pipeline, which systematically links published opsin sequences to compiled in-vivo {lambda}max data, expanding genotype-phenotype coverage and improving prediction, especially for invertebrate opsins with undersampled heterologous data. By integrating accessible software, biologically informed encoding, phylogeny-aware evaluation, and data harmonization, our framework improves confidence, accuracy, and interpretability of genotype-phenotype prediction. An accurate genotype-phenotype map allows simulating molecular evolution of function, reconstructing the history of visual phenotypes, designing functional proteins, and generating new hypotheses that can be tested with heterologous phenotyping.

bioinformatics↗

Discovering genotype-phenotype relationships with machine learning and the Visual Physiology Opsin Database (VPOD)

BackgroundPredicting phenotypes from genetic variation is foundational for fields as diverse as bioengineering and global change biology, highlighting the importance of efficient methods to predict gene functions. Linking genetic changes to phenotypic changes has been a goal of decades of experimental work, especially for some model gene families including light-sensitive opsin proteins. Opsins can be expressed in vitro to measure light absorption parameters, including {lambda}max - the wavelength of maximum absorbance - which strongly affects organismal phenotypes like color vision. Despite extensive research on opsins, the data remain dispersed, uncompiled, and often challenging to access, thereby precluding systematic and comprehensive analyses of the intricate relationships between genotype and phenotype. ResultsHere, we report a newly compiled database of all heterologously expressed opsin genes with {lambda}max phenotypes called the Visual Physiology Opsin Database (VPOD). VPOD_1.0 contains 864 unique opsin genotypes and corresponding {lambda}max phenotypes collected across all animals from 73 separate publications. We use VPOD data and deepBreaks to show regression-based machine learning (ML) models often reliably predict {lambda}max, account for non-additive effects of mutations on function, and identify functionally critical amino acid sites. ConclusionThe ability to reliably predict functions from gene sequences alone using ML will allow robust exploration of molecular-evolutionary patterns governing phenotype, will inform functional and evolutionary connections to an organisms ecological niche, and may be used more broadly for de-novo protein design. Together, our database, phenotype predictions, and model comparisons lay the groundwork for future research applicable to families of genes with quantifiable and comparable phenotypes. Key PointsO_LIWe introduce the Visual Physiology Opsin Database (VPOD_1.0), which includes 864 unique animal opsin genotypes and corresponding {lambda}max phenotypes from 73 separate publications. C_LIO_LIWe demonstrate that regression-based ML models can reliably predict {lambda}max from gene sequence alone, predict non-additive effects of mutations on function, and identify functionally critical amino acid sites. C_LIO_LIWe provide an approach that lays the groundwork for future robust exploration of molecular-evolutionary patterns governing phenotype, with potential broader applications to any family of genes with quantifiable and comparable phenotypes. C_LI

bioinformatics↗