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Abstract
Background: Single-cell RNA-sequencing (scRNA-seq) is becoming indispensable in the study of cell-specific transcriptomes. However, in scRNA-seq techniques, only a small fraction of the genes are captured due to “dropout” events. These dropout events require intensive treatment when analyzing scRNA-seq data. For example, imputation tools have been proposed to estimate dropout events and de-noise data. The performance of these imputation tools are often evaluated, or fine-tuned, using various clustering criteria based on ground-truth cell subgroup labels. This limits their effectiveness in the cases where we lack cell subgroup knowledge. We consider an alternative strategy which requires the imputation to follow a “self-consistency” principle; that is, the imputation process is to refine its results until there is no internal inconsistency or dropouts from the data. Results: We propose the use of “self-consistency” as a main criteria in performing imputation. To demonstrate this principle we devised I-Impute, a “self-consistent” method, to impute scRNA-seq data. I-Impute optimizes continuous similarities and dropout probabilities, in iterative refinements until a self-consistent imputation is reached. On the in silico data sets, I-Impute exhibited the highest Pearson correlations for different dropout rates consistently compared with the state-of-art methods SAVER and scImpute. Furthermore, we collected three wetlab datasets, mouse bladder cells dataset, embryonic stem cells dataset, and aortic leukocyte cells dataset, to evaluate the tools. I-Impute exhibited feasible cell subpopulation discovery efficacy on all the three datasets. It achieves the highest clustering accuracy compared with SAVER and scImpute. Conclusions: A strategy based on “self-consistency”, captured through our method, I-Impute, gave imputation results better than the state-of-the-art tools. Source code of I-Impute can be accessed at https://github.com/xikanfeng2/I-Impute.
Original language | English |
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Article number | 618 |
Journal | BMC Genomics |
Volume | 21 |
Issue number | Suppl. 10 |
Online published | 18 Nov 2020 |
DOIs | |
Publication status | Published - 2020 |
Event | 18th Asia Pacific Bioinformatics Conference (APBC 2020) - Samjung Hotel, Seoul, Korea, Republic of Duration: 18 Aug 2020 → 20 Aug 2020 http://epigenomics.snu.ac.kr/APBC2020/ |
Research Keywords
- scRNA-seq
- Imputation
- Self-consistency
- Cell subpopulation identification
Publisher's Copyright Statement
- This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/
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GRF: Algorithms and Models for Local Genomics Map of Oncogenic Virus Integration
LI, S. (Principal Investigator / Project Coordinator)
1/10/16 → 8/09/20
Project: Research