Evidence map›Paper›PMID 33208097›Full record

ArticleBMC genomics2020

I-Impute: a self-consistent method to impute single cell RNA sequencing data.

Xikang Feng, Lingxi Chen, Zishuai Wang, Shuai Cheng Li

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Article in BMC genomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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3 · Its place in the literature

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4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Xikang FengSchool of Software, Northwestern Polytechnical University, Xi'an, Shaanxi, 710072, China.
Lingxi ChenDepartment of Computer Science, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong, China.
Zishuai WangDepartment of Computer Science, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong, China.
Shuai Cheng LiDepartment of Computer Science, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong, China. shuaicli@cityu.edu.hk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSingle-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.

resultsWe 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.

conclusionsA 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 .

Indexed as

RNASingle-Cell AnalysisAnimalsGene Expression ProfilingMiceSequence Analysis, RNASoftwareRNACell subpopulation identificationImputationscRNA-seqSelf-consistency

Identifiers

PMID33208097
PMCPMC7677776

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.