Timestamp calibration for time-series single cell RNA-seq expression data
Xiran Chen, Sha Lin, Xiaofeng Chen, Weikai Li, Yifei Li

TL;DR
This paper introduces ScPace, a novel timestamp calibration model for noisy time-series single-cell RNA-seq data, improving annotation accuracy and downstream pseudotime analysis by effectively detecting and handling noisy labels.
Contribution
The paper presents a new latent variable-based calibration method, ScPace, that outperforms existing approaches in handling noisy timestamps in time-series scRNA-seq data.
Findings
ScPace outperforms previous methods in simulated and real datasets.
Calibrated timestamps improve pseudotime analysis accuracy.
The method robustly detects and handles noisy labels across datasets.
Abstract
Timestamp automatic annotation (TAA) is a crucial procedure for analyzing time-series ScRNA-seq data, as they unveil dynamic biological developments and cell regeneration process. However, current TAA methods heavily rely on manual timestamps, often overlooking their reliability. This oversight can significantly degrade the performance of timestamp automatic annotation due to noisy timestamps. Nevertheless, the current approach for addressing this issue tends to select less critical cleaned samples for timestamp calibration. To tackle this challenge, we have developed a novel timestamp calibration model called ScPace for handling noisy labeled time-series ScRNA-seq data. This approach incorporates a latent variable indicator within a base classifier instead of probability sampling to detect noisy samples effectively. To validate our proposed method, we conducted experiments on both…
Peer Reviews
No public reviews on file for this paper yet. If you reviewed it on a platform where reviews are public (OpenReview, ICLR, NeurIPS, ICML), you can paste yours below so the community can read it here.
Code & Models
Videos
No videos yet. Explain this paper in a talk, walkthrough, or lecture? Add one.
Taxonomy
TopicsSingle-cell and spatial transcriptomics
MethodsBalanced Selection
