<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Wayment-Steele HK</submitter><funding>NIGMS NIH HHS</funding><pubmed_abstract>Messenger RNA-based medicines hold immense potential, as evidenced by their rapid deployment as COVID-19 vaccines. However, worldwide distribution of mRNA molecules has been limited by their thermostability, which is fundamentally limited by the intrinsic instability of RNA molecules to a chemical degradation reaction called in-line hydrolysis. Predicting the degradation of an RNA molecule is a key task in designing more stable RNA-based therapeutics. Here, we describe a crowdsourced machine learning competition ("Stanford OpenVaccine") on Kaggle, involving single-nucleotide resolution measurements on 6043 102-130-nucleotide diverse RNA constructs that were themselves solicited through crowdsourcing on the RNA design platform Eterna. The entire experiment was completed in less than 6 month</pubmed_abstract><journal>ArXiv</journal><pagination>arXiv:2110.07531v2</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8528079</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Deep learning models for predicting RNA degradation via dual crowdsourcing.</pubmed_title><pmcid>PMC8528079</pmcid><funding_grant_id>R35 GM122579</funding_grant_id><pubmed_authors>Steenwinckel B</pubmed_authors><pubmed_authors>Participants E</pubmed_authors><pubmed_authors>Ito T</pubmed_authors><pubmed_authors>Das R</pubmed_authors><pubmed_authors>Vandewiele G</pubmed_authors><pubmed_authors>Gao J</pubmed_authors><pubmed_authors>Mao H</pubmed_authors><pubmed_authors>Wayment-Steele HK</pubmed_authors><pubmed_authors>Tunguz B</pubmed_authors><pubmed_authors>Fujikawa K</pubmed_authors><pubmed_authors>Kim DS</pubmed_authors><pubmed_authors>Kladwang W</pubmed_authors><pubmed_authors>Ishi K</pubmed_authors><pubmed_authors>Romano J</pubmed_authors><pubmed_authors>Fares M</pubmed_authors><pubmed_authors>Wellington-Oguri R</pubmed_authors><pubmed_authors>Ozturk F</pubmed_authors><pubmed_authors>Tinti M</pubmed_authors><pubmed_authors>Ozturk E</pubmed_authors><pubmed_authors>Watkins AM</pubmed_authors><pubmed_authors>Demkin M</pubmed_authors><pubmed_authors>Chiu A</pubmed_authors><pubmed_authors>He S</pubmed_authors><pubmed_authors>Onodera K</pubmed_authors><pubmed_authors>Noumi T</pubmed_authors><pubmed_authors>Reade W</pubmed_authors><pubmed_authors>Lee Y</pubmed_authors><pubmed_authors>Nicol JJ</pubmed_authors><pubmed_authors>Amer K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Deep learning models for predicting RNA degradation via dual crowdsourcing.</name><description>Messenger RNA-based medicines hold immense potential, as evidenced by their rapid deployment as COVID-19 vaccines. However, worldwide distribution of mRNA molecules has been limited by their thermostability, which is fundamentally limited by the intrinsic instability of RNA molecules to a chemical degradation reaction called in-line hydrolysis. Predicting the degradation of an RNA molecule is a key task in designing more stable RNA-based therapeutics. Here, we describe a crowdsourced machine learning competition ("Stanford OpenVaccine") on Kaggle, involving single-nucleotide resolution measurements on 6043 102-130-nucleotide diverse RNA constructs that were themselves solicited through crowdsourcing on the RNA design platform Eterna. The entire experiment was completed in less than 6 month</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Oct</publication><modification>2026-05-31T03:15:13.601Z</modification><creation>2025-04-06T08:09:50.353Z</creation></dates><accession>S-EPMC8528079</accession><cross_references><pubmed>34671698</pubmed></cross_references></HashMap>