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Narges Zarnaghinaghsh

Publications and source records attributed to Narges Zarnaghinaghsh.

2 recordsLinked to original sources

A Conditional Structure-Aware Generative Transformer for Multi-Objective Design of m1Ψ-Modified RNA 5' UTRs

The 5' untranslated region is a major determinant of translation initiation, and its effect becomes especially important in modified mRNA sequences, where start-codon context, cap-proximal secondary structure, upstream AUGs and upstream open reading frames, and nucleotide chemistry can alter ribosome scanning and initiation recruitment, scanning, and decoding in sequence-dependent ways. Recent computational studies have moved the field from prediction toward design, including massively trained predictive models such as Smart5UTR for m1$Ψ$-modified mRNA, broader 5' UTR generation and optimization frameworks such as UTRGAN and UTailoR, and structure-guided RNA design systems such as RhoDesign. Here, we describe a conditional generative framework for 50-nt modified-RNA 5' UTR design that optionally conditions on ribosome load, GC content, minimum free energy, and target secondary structure. The implementation uses a Transformer-based generator followed by sequence ranking and local refinement with a Smart5UTR-derived ribosome-load oracle and ViennaRNA-based folding metrics, including support for modified-base folding parameters. Across multiple simulation scenarios and experimental settings, different combinations of RL, GC, MFE, and structural constraints produced distinct performance tradeoffs, enabling ablation-based identification of the best-performing formulation.

q-bio.GN

Efficient design of rna sequences with desired properties, structure, and motifs using a grammar variational autoencoder

Designing structurally stable RNA sequences with specific motifs and other desirable properties is an important challenge in bioinformatics. The potential design space increases exponentially with the length of the RNA to be engineered, which makes this a difficult combinatorial optimization problem. In this paper, we propose an RNA grammar variational autoencoder (RGVAE) that can efficiently generate novel RNA sequences with specific target properties. The proposed RGVAE builds on the recently proposed grammar VAE, where we incorporate the stochastic context-free grammar (SCFG) to design strutural RNAs with desired motifs and characteristics. Using the SCFG can ensure that the generated RNA sequence can form a thermodynamically stable secondary structure. Given a RNA sequence, the SCFT is used to find the parse tree, which is represented in a continuous low-dimensional latent space by the RGVAE encoder. We can optimize the RNA in the latent space, where the latent representation can be decoded by the RGVAE decoder to reconstruct the RNA sequence. Based on a number of practical uses cases, we demonstrate that RGVAE can be used to efficiently design structurally stable RNAs with specific target properties, which significantly outperform other alternatives such as randomized design and regular VAEs that do not utilize the SCFG. Code availability: the source code of RGVAE and the data used in this study are provided in https://github.com/nzarnaghinaghsh/RGVAE/tree/main, DOI 10.5281/zenodo.15569206.

q-bio.QM