devCellPy is a machine learning-enabled pipeline for automated annotation of complex multilayered single-cell transcriptomic data.
Francisco Xavier GaldosSidra XuWilliam R GoodyerLauren DuanYuhsin V HuangSoah LeeDarryl LeongCarissa LeeNicholas WeiDaniel LeeSean M WuPublished in: Nature communications (2022)
A major informatic challenge in single cell RNA-sequencing analysis is the precise annotation of datasets where cells exhibit complex multilayered identities or transitory states. Here, we present devCellPy a highly accurate and precise machine learning-enabled tool that enables automated prediction of cell types across complex annotation hierarchies. To demonstrate the power of devCellPy, we construct a murine cardiac developmental atlas from published datasets encompassing 104,199 cells from E6.5-E16.5 and train devCellPy to generate a cardiac prediction algorithm. Using this algorithm, we observe a high prediction accuracy (>90%) across multiple layers of annotation and across de novo murine developmental data. Furthermore, we conduct a cross-species prediction of cardiomyocyte subtypes from in vitro-derived human induced pluripotent stem cells and unexpectedly uncover a predominance of left ventricular (LV) identity that we confirmed by an LV-specific TBX5 lineage tracing system. Together, our results show devCellPy to be a useful tool for automated cell prediction across complex cellular hierarchies, species, and experimental systems.
Keyphrases
- single cell
- rna seq
- machine learning
- high throughput
- left ventricular
- deep learning
- big data
- induced pluripotent stem cells
- artificial intelligence
- heart failure
- endothelial cells
- induced apoptosis
- acute myocardial infarction
- mitral valve
- percutaneous coronary intervention
- data analysis
- oxidative stress
- coronary artery disease
- mesenchymal stem cells
- genetic diversity