<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wayment-Steele HK</submitter><funding>Stanford University</funding><funding>U.S. Department of Health &amp;amp; Human Services | National Institutes of Health</funding><pagination>1174-1184</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9771809</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>4(12)</volume><pubmed_abstract>Medicines based on messenger RNA (mRNA) 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 6,043 diverse 102-130-nucleotide RNA constructs that were themselves solicited through crowdsourcing on the RNA design platform Eterna. The entire experiment was completed in less t</pubmed_abstract><journal>Nature machine intelligence</journal><pubmed_title>Deep learning models for predicting RNA degradation via dual crowdsourcing.</pubmed_title><pmcid>PMC9771809</pmcid><funding_grant_id>R35 GM122579</funding_grant_id><funding_grant_id>RISE</funding_grant_id><pubmed_authors>Steenwinckel B</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>Chiu KY</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>Eterna Participants</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>Medicines based on messenger RNA (mRNA) 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 6,043 diverse 102-130-nucleotide RNA constructs that were themselves solicited through crowdsourcing on the RNA design platform Eterna. The entire experiment was completed in less t</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-25T19:59:06.861Z</modification><creation>2025-02-19T01:08:01.465Z</creation></dates><accession>S-EPMC9771809</accession><cross_references><pubmed>36567960</pubmed><doi>10.1038/s42256-022-00571-8</doi></cross_references></HashMap>