scReClassify

scReClassify refines post hoc cell type annotations in single-cell RNA sequencing (scRNA-seq) datasets using a semi-supervised adaSampling approach to identify and correct mislabeled cells.


Key Features:

  • Semi-Supervised Learning Framework: Employs a semi-supervised approach that leverages both labeled and unlabeled scRNA-seq data to improve annotation accuracy.
  • Dimension Reduction via PCA: Uses Principal Component Analysis (PCA) for dimension reduction to preserve key variance in complex scRNA-seq datasets prior to classification.
  • Adaptive Sampling Algorithm (adaSampling): Implements the adaSampling algorithm to detect and reclassify mislabeled cells into their most probable cell types.
  • Post hoc Reclassification: Performs post hoc refinement of initial cell type annotations to address mislabeling arising from incomplete biological knowledge or subjective inspection.
  • Validation on Simulated and Experimental Data: Has been validated on both simulated and real-world experimental datasets across multiple tissues and biological systems.

Scientific Applications:

  • Developmental Biology: Provides more accurate cell type classifications for studying cellular differentiation and developmental processes.
  • Cell Reprogramming: Enhances precision in identifying reprogrammed cells for regenerative medicine and stem cell research.
  • Cancer Research: Improves discrimination between cancerous and non-cancerous cell types to aid studies of tumor heterogeneity.

Methodology:

Applies Principal Component Analysis (PCA) for dimension reduction followed by a semi-supervised adaSampling algorithm that leverages labeled and unlabeled scRNA-seq data to identify and reclassify mislabeled cells; validation used simulated and real-world experimental datasets.

Topics

Details

Programming Languages:
R
Added:
1/14/2020
Last Updated:
12/18/2020

Operations

Publications

Kim T, Lo K, Geddes TA, Kim HJ, Yang JYH, Yang P. scReClassify: post hoc cell type classification of single-cell rNA-seq data. BMC Genomics. 2019;20(S9). doi:10.1186/s12864-019-6305-x. PMID:31874628. PMCID:PMC6929456.