Evidence map›Paper›PMID 38352531›Full record

ArticlebioRxiv : the preprint server for biology2024

RNA3DB: A structurally-dissimilar dataset split for training and benchmarking deep learning models for RNA structure prediction.

Marcell Szikszai, Marcin Magnus, Siddhant Sanghi, Sachin Kadyan, Nazim Bouatta, Elena Rivas

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In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Marcell SzikszaiDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, 02138, MA, USA.
Marcin MagnusDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, 02138, MA, USA.
Siddhant SanghiDepartment of Systems Biology, Columbia University, New York, 10027, NY, USA.
Sachin KadyanDepartment of Systems Biology, Columbia University, New York, 10027, NY, USA.
Nazim BouattaLaboratory of Systems Pharmacology, Harvard Medical School, Boston, 02115, MA, USA.
Elena RivasDepartment of Molecular and Cellular Biology, Harvard University, Cambridge, 02138, MA, USA.ORCID 0000-0002-2084-269X

Funding

Discovery of structural RNAs involved in human health and diseaseR01GM144423 · NIGMS · HARVARD UNIVERSITY · PI RIVAS, ELENA · 2022 to 2025
$1.4M
An all-in-one web server for RNA structure prediction using evolutionary informationR21GM148902 · NIGMS · HARVARD UNIVERSITY · PI RIVAS, ELENA, VICENS, QUENTIN · 2023 to 2024
$415k
NIGMS NIH HHS R01 GM144423NIGMS NIH HHS R21 GM148902
6 · The paper itself

Abstract

With advances in protein structure prediction thanks to deep learning models like AlphaFold, RNA structure prediction has recently received increased attention from deep learning researchers. RNAs introduce substantial challenges due to the sparser availability and lower structural diversity of the experimentally resolved RNA structures in comparison to protein structures. These challenges are often poorly addressed by the existing literature, many of which report inflated performance due to using training and testing sets with significant structural overlap. Further, the most recent Critical Assessment of Structure Prediction (CASP15) has shown that deep learning models for RNA structure are currently outperformed by traditional methods. In this paper we present RNA3DB, a dataset of structured RNAs, derived from the Protein Data Bank (PDB), that is designed for training and benchmarking deep learning models. The RNA3DB method arranges the RNA 3D chains into distinct groups (Components) that are non-redundant both with regard to sequence as well as structure, providing a robust way of dividing training, validation, and testing sets. Any split of these structurally-dissimilar Components are guaranteed to produce test and validations sets that are distinct by sequence and structure from those in the training set. We provide the RNA3DB dataset, a particular train/test split of the RNA3DB Components (in an approximate 70/30 ratio) that will be updated periodically. We also provide the RNA3DB methodology along with the source-code, with the goal of creating a reproducible and customizable tool for producing structurally-dissimilar dataset splits for structural RNAs.

Identifiers

PMID38352531
PMCPMC10862857

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.