<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Wang XJ</submitter><funding>Schwartz/Reisman Collaborative Science Program</funding><funding>Heritage Medical Research Institute</funding><funding>Pew-Stewart Cancer Scholars program</funding><funding>Israeli Council for Higher Education (CHE) via the Weizmann Data Science Research Center</funding><funding>Gordon and Betty Moore Foundation</funding><funding>National Institutes of Health</funding><funding>HHMI Freeman Hrabowski Scholar Program</funding><funding>Rita Allen Foundation</funding><funding>Susan E Riley Foundation</funding><funding>Shurl and Kay Curci Foundation</funding><funding>Schmidt Academy for Software Engineering</funding><funding>Abisch-Frenkel foundation</funding><funding>Enoch foundation research fund</funding><funding>Sharon Levine Foundation</funding><funding>European Research Council</funding><funding>Rising Tide foundation</funding><funding>Israel Science Foundation</funding><funding>NIH HHS</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>We present DeepCell Types, a novel approach to cell phenotyping for spatial proteomics that addresses the challenge of generalization across diverse datasets with varying marker panels collected across different platforms. Our approach utilizes a transformer with channel-wise attention to create a language-informed vision model; this model's semantic understanding of the underlying marker panel enables it to learn from and adapt to heterogeneous datasets. Leveraging a curated, diverse dataset named Expanded TissueNet with cell type labels spanning the literature and the NIH Human BioMolecular Atlas Program (HuBMAP) consortium, our model demonstrates robust performance across various cell types, tissues, and imaging modalities. Comprehensive benchmarking shows superior accuracy and generali</pubmed_abstract><journal>bioRxiv : the preprint server for biology</journal><pagination>2024.11.02.621624</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11601246</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Generalized cell phenotyping for spatial proteomics with language-informed vision models.</pubmed_title><pmcid>PMC11601246</pmcid><funding_grant_id>948811</funding_grant_id><funding_grant_id>OT2OD033759</funding_grant_id><funding_grant_id>DP2-GM149556</funding_grant_id><funding_grant_id>OT2 OD033759</funding_grant_id><funding_grant_id>DP2 GM149556</funding_grant_id><funding_grant_id>OT2 OD033756</funding_grant_id><funding_grant_id>OT2OD033756</funding_grant_id><funding_grant_id>2481/20</funding_grant_id><funding_grant_id>3830/21</funding_grant_id><pubmed_authors>Abt M</pubmed_authors><pubmed_authors>Bussi Y</pubmed_authors><pubmed_authors>Pradhan E</pubmed_authors><pubmed_authors>Van Valen D</pubmed_authors><pubmed_authors>Borner K</pubmed_authors><pubmed_authors>Yu K</pubmed_authors><pubmed_authors>Wang XJ</pubmed_authors><pubmed_authors>Brown C</pubmed_authors><pubmed_authors>Keren L</pubmed_authors><pubmed_authors>Barnowski R</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Iqbal AR</pubmed_authors><pubmed_authors>Dilip R</pubmed_authors><pubmed_authors>Jain Y</pubmed_authors><pubmed_authors>Yue Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Generalized cell phenotyping for spatial proteomics with language-informed vision models.</name><description>We present DeepCell Types, a novel approach to cell phenotyping for spatial proteomics that addresses the challenge of generalization across diverse datasets with varying marker panels collected across different platforms. Our approach utilizes a transformer with channel-wise attention to create a language-informed vision model; this model's semantic understanding of the underlying marker panel enables it to learn from and adapt to heterogeneous datasets. Leveraging a curated, diverse dataset named Expanded TissueNet with cell type labels spanning the literature and the NIH Human BioMolecular Atlas Program (HuBMAP) consortium, our model demonstrates robust performance across various cell types, tissues, and imaging modalities. Comprehensive benchmarking shows superior accuracy and generali</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Aug</publication><modification>2026-05-23T03:24:58.365Z</modification><creation>2025-04-03T23:55:48.37Z</creation></dates><accession>S-EPMC11601246</accession><cross_references><pubmed>39605651</pubmed><doi>10.1101/2024.11.02.621624</doi></cross_references></HashMap>