Your browser doesn't support javascript.
loading
scROSHI: robust supervised hierarchical identification of single cells.
Prummer, Michael; Bertolini, Anne; Bosshard, Lars; Barkmann, Florian; Yates, Josephine; Boeva, Valentina; Stekhoven, Daniel; Singer, Franziska.
Afiliación
  • Prummer M; Nexus Personalized Health Technologies, ETH Zurich, Zurich, Switzerland.
  • Bertolini A; Swiss Institute of Bioinformatics (SIB), Zurich, Switzerland.
  • Bosshard L; Nexus Personalized Health Technologies, ETH Zurich, Zurich, Switzerland.
  • Barkmann F; Swiss Institute of Bioinformatics (SIB), Zurich, Switzerland.
  • Yates J; Nexus Personalized Health Technologies, ETH Zurich, Zurich, Switzerland.
  • Boeva V; Swiss Institute of Bioinformatics (SIB), Zurich, Switzerland.
  • Stekhoven D; Institute for Machine Learning, Department of Computer Science, ETH Zurich, Zurich, Switzerland.
  • Singer F; Swiss Institute of Bioinformatics (SIB), Zurich, Switzerland.
NAR Genom Bioinform ; 5(2): lqad058, 2023 Jun.
Article en En | MEDLINE | ID: mdl-37332656
Identifying cell types based on expression profiles is a pillar of single cell analysis. Existing machine-learning methods identify predictive features from annotated training data, which are often not available in early-stage studies. This can lead to overfitting and inferior performance when applied to new data. To address these challenges we present scROSHI, which utilizes previously obtained cell type-specific gene lists and does not require training or the existence of annotated data. By respecting the hierarchical nature of cell type relationships and assigning cells consecutively to more specialized identities, excellent prediction performance is achieved. In a benchmark based on publicly available PBMC data sets, scROSHI outperforms competing methods when training data are limited or the diversity between experiments is large.

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: NAR Genom Bioinform Año: 2023 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: NAR Genom Bioinform Año: 2023 Tipo del documento: Article