ELeFHAnt: A supervised machine learning approach for label harmonization and annotation of single cell RNA-seq data
Chatuverdi, P.; Zorn, A.; Thorner, K.
Show abstract
Annotation of single cells has become an important step in the single cell analysis framework. With advances in sequencing technology thousands to millions of cells can be processed to understand the intricacies of the biological system in question. Annotation through manual curation of markers based on a priori knowledge is cumbersome given this exponential growth. There are currently ~200 computational tools available to help researchers automatically annotate single cells using supervised/unsupervised machine learning, cell type markers, or tissue-based markers from bulk RNA-seq. But with the expansion of publicly available data there is also a need for a tool which can help integrate multiple references into a unified atlas and understand how annotations between datasets compare. Here we present ELeFHAnt: Ensemble learning for harmonization and annotation of single cells. ELeFHAnt is an easy-to-use R package that employs support vector machine and random forest algorithms together to perform three main functions: 1) CelltypeAnnotation 2) LabelHarmonization 3) DeduceRelationship. CelltypeAnnotation is a function to annotate cells in a query Seurat object using a reference Seurat object with annotated cell types. LabelHarmonization can be utilized to integrate multiple cell atlases (references) into a unified cellular atlas with harmonized cell types. Finally, DeduceRelationship is a function that compares cell types between two scRNA-seq datasets. ELeFHAnt can be accessed from GitHub at https://github.com/praneet1988/ELeFHAnt.
Matching journals
The top 6 journals account for 50% of the predicted probability mass.
Similar papers in this journal
Similar papers in this journal
- Flexible comparison of batch correction methods for single-cell RNA-seq using BatchBench 96%
- MarcoPolo: a clustering-free approach to the exploration of differentially expressed genes along with group information in single-cell RNA-seq data 96%
- CelLink: integrating single-cell multi-omics data with weak feature linkage and imbalanced cell populations 95%
Similar papers in this journal
Similar papers in this journal
- Decoding Single-Cell Multiomics: scMaui - A Deep Learning Framework for Uncovering Cellular Heterogeneity in Presence of Batch Effects and Missing Data 95%
- SC2Spa: a deep learning based approach to map transcriptome to spatial origins at cellular resolution 95%
- On the importance of data transformation for data integration in single-cell RNA sequencing analysis 95%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.