<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Carazo F</submitter><funding>Eusko Jaurlaritza</funding><funding>Provincial Council of Gipuzkoa</funding><pagination>521</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6592009</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Splicing is a genetic process that has important implications in several diseases including cancer. Deciphering the complex rules of splicing regulation is crucial to understand and treat splicing-related diseases. Splicing factors and other RNA-binding proteins (RBPs) play a key role in the regulation of splicing. The specific binding sites of an RBP can be measured using CLIP experiments. However, to unveil which RBPs regulate a condition, it is necessary to have a priori hypotheses, as a single CLIP experiment targets a single protein.&lt;h4>Results&lt;/h4>In this work, we present a novel methodology to predict context-specific splicing factors from transcriptomic data. For this, we systematically collect, integrate and analyze more than 900 CLIP experiments stored in four </pubmed_abstract><journal>BMC genomics</journal><pubmed_title>Integration of CLIP experiments of RNA-binding proteins: a novel approach to predict context-dependent splicing factors from transcriptomic data.</pubmed_title><pmcid>PMC6592009</pmcid><funding_grant_id>MINEDRUG project: “Predicting therapy response in oncology using Big Data analysis&amp;quot;</funding_grant_id><funding_grant_id>MINEDRUG project: "Predicting therapy response in oncology using Big Data analysis"</funding_grant_id><funding_grant_id>PRE_2017_2_0033</funding_grant_id><pubmed_authors>Ferrer-Bonsoms JA</pubmed_authors><pubmed_authors>Rubio A</pubmed_authors><pubmed_authors>Carazo F</pubmed_authors><pubmed_authors>Gimeno M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Integration of CLIP experiments of RNA-binding proteins: a novel approach to predict context-dependent splicing factors from transcriptomic data.</name><description>&lt;h4>Background&lt;/h4>Splicing is a genetic process that has important implications in several diseases including cancer. Deciphering the complex rules of splicing regulation is crucial to understand and treat splicing-related diseases. Splicing factors and other RNA-binding proteins (RBPs) play a key role in the regulation of splicing. The specific binding sites of an RBP can be measured using CLIP experiments. However, to unveil which RBPs regulate a condition, it is necessary to have a priori hypotheses, as a single CLIP experiment targets a single protein.&lt;h4>Results&lt;/h4>In this work, we present a novel methodology to predict context-specific splicing factors from transcriptomic data. For this, we systematically collect, integrate and analyze more than 900 CLIP experiments stored in four </description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jun</publication><modification>2025-05-18T11:02:44.26Z</modification><creation>2025-05-18T11:02:44.26Z</creation></dates><accession>S-EPMC6592009</accession><cross_references><pubmed>31238884</pubmed><doi>10.1186/s12864-019-5900-1</doi></cross_references></HashMap>