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ABSTRACT: Summary
Single-cell data are being generated at an accelerating pace. How best to project data across single-cell atlases is an open problem. We developed a boosted learner that overcomes the greatest challenge with status quo classifiers: low sensitivity, especially when dealing with rare cell types. By comparing novel and published data from distinct scRNA-seq modalities that were acquired from the same tissues, we show that this approach preserves cell-type labels when mapping across diverse platforms.Availability and implementation
https://github.com/diazlab/ELSA.Contact
aaron.diaz@ucsf.edu.Supplementary information
Supplementary data are available at Bioinformatics online.
SUBMITTER: Wang L
PROVIDER: S-EPMC7267838 | biostudies-literature |
REPOSITORIES: biostudies-literature