Scientific publications
JIND: Joint Integration and Discrimination for Automated Single-Cell Annotation. Scientific Publication
Mohit Goyal 1 , Guillermo Serrano 2 , Josepmaria Argemi 3 4 5 6 , Ilan Shomorony 1 , Mikel Hernaez 2 7 8 , Idoia Ochoa 1 8 9
Motivation: An important step in the transcriptomic analysis of individual cells involves manually determining the cellular identities. To ease this labor-intensive annotation of cell-types, there has been a growing interest in automated cell annotation, which can be achieved by training classification algorithms on previously annotated datasets.
Existing pipelines employ dataset integration methods in order to remove potential batch effects between source (annotated) and target (unannotated) datasets. However, the integration and classification steps are usually independent of each other and performed by different tools. We propose JIND, a neural-network-based framework for automated cell-type identification that performs integration in a space suitably chosen to facilitate cell classification.
To account for batch effects, JIND performs a novel asymmetric alignment in which unseen cells are mapped onto the previously learned latent space, avoiding the need of retraining the classification model for new datasets. JIND also learns cell-type-specific confidence thresholds to identify cells that cannot be reliably classified.
Results: We show on several batched datasets that the joint approach to integration and classification of JIND outperforms in accuracy existing pipelines, and a smaller fraction of cells is rejected as unlabeled as a result of the cell-specific confidence thresholds. Moreover, we investigate cells misclassified by JIND and provide evidence suggesting that they could be due to outliers in the annotated datasets or errors in the original approach used for annotation of the target batch.
Availability: Implementation for JIND is available at https://github.com/mohit1997/JIND and at https://doi.org/10.5281/zenodo.6246322.
CITATION Bioinformatics. 2022 Apr 28;38(9):2488-2495. doi: 10.1093/bioinformatics/btac140.