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Vetrov, D.

Publications and source records attributed to Vetrov, D..

2 recordsLinked to original sources

Towards Robust Evaluation of Protein Generative Models: A Systematic Analysis of Metrics

AO_SCPLOWBSTRACTC_SCPLOWThe rapid advancement of protein generative models necessitates robust and principled methods for their evaluation and comparison. As new models of increasing complexity continue to emerge, it is crucial to ensure that the metrics used for assessment are well-understood and reliable. In this work, we conduct a systematic investigation of commonly used metrics for evaluating protein generative models, focusing on quality, diversity, and distributional similarity. We examine the behavior of these metrics under various conditions, including synthetic perturbations and real-world generative models. Our analysis explores different design choices, parameters, and underlying representation models, revealing how these factors influence metric performance. We identify several challenges in applying these metrics, such as sample size dependencies, sensitivity to data distribution shifts, and computational efficiency trade-offs. By testing metrics on both synthetic datasets with controlled properties and outputs from state-of-the-art protein generators, we provide insights into each metrics strengths, limitations, and practical applicability. Based on our findings, we offer a set of practical recommendations for researchers to consider when evaluating protein generative models, aiming to contribute to the development of more robust and meaningful evaluation practices in the field of protein design.

bioinformatics↗

Finemap-MiXeR: A variational Bayesian approach for genetic finemapping

Discoveries from genome-wide association studies often contain large clusters of highly correlated genetic variants, which makes them hard to interpret. In such cases, finemapping the underlying causal variants become important. Here we present a new method, the Finemap-MiXeR, based on a variational Bayesian approach for finemapping genomic data, i.e., determining the causal single nucleotide polymorphisms (SNPs) associated with a trait at a given locus after controlling for correlation among genetic variants due to linkage disequilibrium. Our approach is based on the optimization of Evidence Lower Bound of the likelihood function obtained from the MiXeR model. The optimization is done using Adaptive Moment Estimation Algorithm, allowing to obtain posterior probability of each SNP to be a causal variant. We tested Finemap-MiXeR in a range of different scenarios, using both synthetic and real data from the UK Biobank, using standing height phenotype as an example. In comparison to the existing finemapping methods FINEMAP and SuSiE methods, we observed that Finemap-MiXeR in most cases has better accuracy. Furthermore, it is computationally efficient, and unlike other methods the complexity is not increasing as the number of causal SNPs or the heritability increases. We show that our finemapping algorithm identifies a small number of genetic variants per locus which are informative for predicting the phenotype in an independent sample.

bioinformatics↗