<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ochoteco Asensio J</submitter><funding>Seventh Framework Programme</funding><pagination>2057-2069</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9077535</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20</volume><pubmed_abstract>Proteins are often considered the main biological element in charge of the different functions and structures of a cell. However, proteomics, the global study of all expressed proteins, often performed by mass spectrometry, is limited by its stochastic sampling and can only quantify a limited amount of protein per sample. Transcriptomics, which allows an exhaustive analysis of all expressed transcripts, is often used as a surrogate. However, the transcript level does not present a high level of correlation with the corresponding protein level, notably due to the existence of several post-transcriptional regulatory mechanisms. In this publication, we hypothesize that the missing protein values in proteomics could be predicted using machine learning regression methods, trained with many feat</pubmed_abstract><journal>Computational and structural biotechnology journal</journal><pubmed_title>Predicting missing proteomics values using machine learning: Filling the gap using transcriptomics and other biological features.</pubmed_title><pmcid>PMC9077535</pmcid><funding_grant_id>602156</funding_grant_id><pubmed_authors>Caiment F</pubmed_authors><pubmed_authors>Ochoteco Asensio J</pubmed_authors><pubmed_authors>Verheijen M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Predicting missing proteomics values using machine learning: Filling the gap using transcriptomics and other biological features.</name><description>Proteins are often considered the main biological element in charge of the different functions and structures of a cell. However, proteomics, the global study of all expressed proteins, often performed by mass spectrometry, is limited by its stochastic sampling and can only quantify a limited amount of protein per sample. Transcriptomics, which allows an exhaustive analysis of all expressed transcripts, is often used as a surrogate. However, the transcript level does not present a high level of correlation with the corresponding protein level, notably due to the existence of several post-transcriptional regulatory mechanisms. In this publication, we hypothesize that the missing protein values in proteomics could be predicted using machine learning regression methods, trained with many feat</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-31T20:59:43.847Z</modification><creation>2025-02-19T04:21:03.794Z</creation></dates><accession>S-EPMC9077535</accession><cross_references><pubmed>35601960</pubmed><doi>10.1016/j.csbj.2022.04.017</doi></cross_references></HashMap>