CellSavior: an open-source framework for improved cell calling in targeted single-cell DNA sequencing
Related Experiment Video
Updated: Nov 11, 2026

Detection of Copy Number Alterations Using Single Cell Sequencing
Published on: February 17, 2017
Taehyeon Kim1, Young-Soo Chung2,3,4, Dongwoo Park1
1Department of Biomedical Systems Informatics, Graduate School of Medical Science, Brain Korea 21 FOUR Project, Yonsei University College of Medicine, Seoul 03722, Republic of Korea.
Motivation:
Single-cell DNA sequencing (scDNA-seq) has emerged as a key approach for studying complex genomic variation, including tumor heterogeneity. Despite its increasing commercial availability, exemplified by the Tapestri platform, analytical reproducibility remains limited due to reliance on proprietary and non-transparent pipelines. Among preprocessing steps, cell calling is particularly critical, as it determines which barcodes correspond to true cells rather than background noise and directly shapes all downstream analyses. However, existing methods typically rely on empirical thresholding and exhibit inconsistent performance across datasets. These limitations underscore the need for a robust and generalizable cell calling framework for reliable scDNA-seq analysis.
Results:
We developed CellSavior, an open-source cell calling algorithm with an integrated downstream pipeline that produces standardized outputs. CellSavior employs an ensemble clustering strategy across multiple distance metrics, combined with confidence-weighted merging, to generate a consensus classification that reduces bias and improves robustness. Across 33 public and in-house single-cell DNA sequencing datasets, CellSavior recapitulated cell annotations generated by commercial software (CellFinder) in 31 cases (93.9%). In the remaining discordant cases, CellSavior yielded more biologically interpretable annotations, rescuing previously undetected clusters enriched for key hotspot genomic alterations.
Availability:
The source code for CellSavior is freely available at https://github.com/dauer-tgilab/CellSavior; DOI: https://doi.org/10.5281/zenodo.22744146.
Supplementary Information:
Supplementary data are available at Bioinformatics online.
Related Concept Videos
Cell Lines
Next-generation Sequencing
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.
Sanger Sequencing
RNA-seq
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...
Cell Diversity
Multicellular organisms...
Cell Culture

