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dc.contributor.authorMurphy, Michael
dc.contributor.authorJegelka, Stefanie
dc.contributor.authorFraenkel, Ernest
dc.date.accessioned2023-01-31T19:11:55Z
dc.date.available2023-01-31T19:11:55Z
dc.date.issued2022-06-24
dc.identifier.urihttps://hdl.handle.net/1721.1/147819
dc.description.abstract<jats:title>Abstract</jats:title> <jats:sec> <jats:title>Motivation</jats:title> <jats:p>Advances in bioimaging now permit in situ proteomic characterization of cell–cell interactions in complex tissues, with important applications across a spectrum of biological problems from development to disease. These methods depend on selection of antibodies targeting proteins that are expressed specifically in particular cell types. Candidate marker proteins are often identified from single-cell transcriptomic data, with variable rates of success, in part due to divergence between expression levels of proteins and the genes that encode them. In principle, marker identification could be improved by using existing databases of immunohistochemistry for thousands of antibodies in human tissue, such as the Human Protein Atlas. However, these data lack detailed annotations of the types of cells in each image.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>We develop a method to predict cell type specificity of protein markers from unlabeled images. We train a convolutional neural network with a self-supervised objective to generate embeddings of the images. Using non-linear dimensionality reduction, we observe that the model clusters images according to cell types and anatomical regions for which the stained proteins are specific. We then use estimates of cell type specificity derived from an independent single-cell transcriptomics dataset to train an image classifier, without requiring any human labelling of images. Our scheme demonstrates superior classification of known proteomic markers in kidney compared to selection via single-cell transcriptomics.</jats:p> </jats:sec> <jats:sec> <jats:title>Availability and implementation</jats:title> <jats:p>Code and trained model are available at www.github.com/murphy17/HPA-SimCLR.</jats:p> </jats:sec> <jats:sec> <jats:title>Supplementary information</jats:title> <jats:p>Supplementary data are available at Bioinformatics online.</jats:p> </jats:sec>en_US
dc.language.isoen
dc.publisherOxford University Press (OUP)en_US
dc.relation.isversionof10.1093/bioinformatics/btac263en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceOxford University Pressen_US
dc.titleSelf-supervised learning of cell type specificity from immunohistochemical imagesen_US
dc.typeArticleen_US
dc.identifier.citationMurphy, Michael, Jegelka, Stefanie and Fraenkel, Ernest. 2022. "Self-supervised learning of cell type specificity from immunohistochemical images." Bioinformatics, 38 (Supplement_1).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.relation.journalBioinformaticsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2023-01-31T18:58:14Z
dspace.orderedauthorsMurphy, M; Jegelka, S; Fraenkel, Een_US
dspace.date.submission2023-01-31T18:58:15Z
mit.journal.volume38en_US
mit.journal.issueSupplement_1en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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