<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yao S</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>Division of Chemistry</funding><funding>Office of the Vice President for Research and Partnerships</funding><funding>NIAID NIH HHS</funding><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><pagination>19238-19247</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11673283</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>96(49)</volume><pubmed_abstract>Single-cell mass spectrometry (SCMS) is an emerging tool for studying cell heterogeneity according to variation of molecular species in single cells. Although it has become increasingly common to employ machine learning models in SCMS data analysis, such as the classification of cell phenotypes, the existing machine learning models often suffer from low adaptability and transferability. In addition, SCMS studies of rare cells can be restricted by limited number of cell samples. To overcome these limitations, we performed SCMS analyses of melanoma cancer cell lines with two phenotypes (i.e., primary and metastatic cells). We then developed a meta-learning-based model, MetaPhenotype, that can be trained using a small amount of SCMS data to accurately classify cells into primary or metastatic</pubmed_abstract><journal>Analytical chemistry</journal><pubmed_title>MetaPhenotype: A Transferable Meta-Learning Model for Single-Cell Mass Spectrometry-Based Cell Phenotype Prediction Using Limited Number of Cells.</pubmed_title><pmcid>PMC11673283</pmcid><funding_grant_id>R01AI177469</funding_grant_id><funding_grant_id>R01 GM135392</funding_grant_id><funding_grant_id>R01GM135392</funding_grant_id><funding_grant_id>R01 AI177469</funding_grant_id><funding_grant_id>2305182</funding_grant_id><pubmed_authors>Yang W</pubmed_authors><pubmed_authors>Nguyen TD</pubmed_authors><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Shao Y</pubmed_authors><pubmed_authors>Yao S</pubmed_authors><pubmed_authors>Lan Y</pubmed_authors><pubmed_authors>Chen D</pubmed_authors></additional><is_claimable>false</is_claimable><name>MetaPhenotype: A Transferable Meta-Learning Model for Single-Cell Mass Spectrometry-Based Cell Phenotype Prediction Using Limited Number of Cells.</name><description>Single-cell mass spectrometry (SCMS) is an emerging tool for studying cell heterogeneity according to variation of molecular species in single cells. Although it has become increasingly common to employ machine learning models in SCMS data analysis, such as the classification of cell phenotypes, the existing machine learning models often suffer from low adaptability and transferability. In addition, SCMS studies of rare cells can be restricted by limited number of cell samples. To overcome these limitations, we performed SCMS analyses of melanoma cancer cell lines with two phenotypes (i.e., primary and metastatic cells). We then developed a meta-learning-based model, MetaPhenotype, that can be trained using a small amount of SCMS data to accurately classify cells into primary or metastatic</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Dec</publication><modification>2025-04-04T01:33:15.919Z</modification><creation>2025-04-04T01:33:15.919Z</creation></dates><accession>S-EPMC11673283</accession><cross_references><pubmed>39570119</pubmed><doi>10.1021/acs.analchem.4c02038</doi></cross_references></HashMap>