Evidence map›Paper›PMID 38000911›Full record

ArticleGigaScience2022

Imputation method for single-cell RNA-seq data using neural topic model.

Yueyang Qi, Shuangkai Han, Lin Tang, Lin Liu

Abstract read
In one paragraph

Article in GigaScience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Yueyang QiYunnan Normal University, School of Information, Kunming 650500, China.ORCID 0009-0006-3210-6055
Shuangkai HanYunnan Normal University, School of Information, Kunming 650500, China.ORCID 0009-0002-9337-5890
Lin TangYunnan Normal University, Faculty of Education, Kunming 650500, China.
Lin LiuYunnan Normal University, School of Information, Kunming 650500, China.ORCID 0000-0002-8773-6162

Funding

National Natural Science Foundation of China 61862067
6 · The paper itself

Abstract

Single-cell RNA sequencing (scRNA-seq) technology studies transcriptome and cell-to-cell differences from higher single-cell resolution and different perspectives. Despite the advantage of high capture efficiency, downstream functional analysis of scRNA-seq data is made difficult by the excess of zero values (i.e., the dropout phenomenon). To effectively address this problem, we introduced scNTImpute, an imputation framework based on a neural topic model. A neural network encoder is used to extract underlying topic features of single-cell transcriptome data to infer high-quality cell similarity. At the same time, we determine which transcriptome data are affected by the dropout phenomenon according to the learning of the mixture model by the neural network. On the basis of stable cell similarity, the same gene information in other similar cells is borrowed to impute only the missing expression values. By evaluating the performance of real data, scNTImpute can accurately and efficiently identify the dropout values and imputes them accurately. In the meantime, the clustering of cell subsets is improved and the original biological information in cell clustering is solved, which is covered by technical noise. The source code for the scNTImpute module is available as open source at https://github.com/qiyueyang-7/scNTImpute.git.

Indexed as

Single-Cell AnalysisSingle-Cell Gene Expression AnalysisCluster AnalysisGene Expression ProfilingSequence Analysis, RNASoftwareTranscriptomedropoutimputationneural topic modelSingle-cell RNA sequencing

Identifiers

PMID38000911
PMCPMC10673642

What OpenQuestion holds

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LicenceCC BY
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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.