eHSCPr

eHSCPr predicts early hematopoietic stem cell (HSC) developmental stages from single-cell transcriptomic data using machine learning.


Key Features:

  • Input data: Processes large-scale single-cell transcriptomic datasets.
  • Gene selection (F-score comparison): Uses the F-score for differential gene selection and compares it with limma, DESeq2, and edgeR, reporting an ROC AUC of 0.987 for selected markers.
  • Surface marker identification: Identifies critical surface markers for endothelial cells and hematopoietic cells.
  • Classifier: Implements a support vector machine (SVM)-based classifier.
  • Validation metrics: Reports 10-fold cross-validation accuracies of 94.19% on the training dataset and 94.84% on an independent dataset, alongside ROC AUC values.
  • Transcription analysis: Performs transcription analysis on the F-score gene set to enrich signal markers associated with HSC developmental stages.

Scientific Applications:

  • Early HSC stage prediction: Predicts early developmental stages of hematopoietic stem cells from single-cell data.
  • Surface marker selection: Selects candidate surface markers for endothelial and hematopoietic cell populations.
  • In vitro blood regeneration: Provides marker and stage predictions to inform in vitro blood regeneration studies.
  • Extracorporeal blood research: Supports extracorporeal blood research by identifying early HSC developmental signatures.
  • Experimental design support: Supports hypothesis-driven experimental design through computational marker and stage predictions.

Methodology:

Processes single-cell transcriptomic data with machine learning using F-score-based differential gene selection compared against limma, DESeq2, and edgeR, applies a support vector machine (SVM) classifier with 10-fold cross-validation, and conducts transcription analysis on the F-score gene set.

Topics

Details

Tool Type:
web application
Added:
3/19/2021
Last Updated:
5/5/2021

Operations

Publications

Wang H, Liang P, Zheng L, Long C, Li H, Zuo Y. eHSCPr discriminating the cell identity involved in endothelial to hematopoietic transition. Bioinformatics. 2021;37(15):2157-2164. doi:10.1093/bioinformatics/btab071. PMID:33532815.

PMID: 33532815
Funding: - National Nature Scientific Foundation of China: 61702290, 61861036, 62061034 - Program for Young Talents of Science and Technology in Universities of Inner Mongolia Autonomous Region: NJYT-18-B01 - Fund for Excellent Young Scholars of Inner Mongolia: 2017JQ04