Evidence map›Paper›PMID 38493095›Full record

ArticleBMC bioinformatics2024

Integration of scRNA-seq data by disentangled representation learning with condition domain adaptation.

Renjing Liu, Kun Qian, Xinwei He, Hongwei Li

Abstract read
In one paragraph

Article in BMC bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 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.

Renjing Liu *School of Mathematics and Physics, China University of Geosciences (Wuhan), Wuhan, 430074, China.
Kun Qian *School of Mathematics and Physics, China University of Geosciences (Wuhan), Wuhan, 430074, China.
Xinwei HeSchool of Mathematics and Physics, China University of Geosciences (Wuhan), Wuhan, 430074, China.
Hongwei LiSchool of Mathematics and Physics, China University of Geosciences (Wuhan), Wuhan, 430074, China. hwli@cug.edu.cn.

Funding

National Natural Science Foundation of China No.42374174 and No.42274172
6 · The paper itself

Abstract

backgroundThe integration of single-cell RNA sequencing data from multiple experimental batches and diverse biological conditions holds significant importance in the study of cellular heterogeneity.

resultsTo expedite the exploration of systematic disparities under various biological contexts, we propose a scRNA-seq integration method called scDisco, which involves a domain-adaptive decoupling representation learning strategy for the integration of dissimilar single-cell RNA data. It constructs a condition-specific domain-adaptive network founded on variational autoencoders. scDisco not only effectively reduces batch effects but also successfully disentangles biological effects and condition-specific effects, and further augmenting condition-specific representations through the utilization of condition-specific Domain-Specific Batch Normalization layers. This enhancement enables the identification of genes specific to particular conditions. The effectiveness and robustness of scDisco as an integration method were analyzed using both simulated and real datasets, and the results demonstrate that scDisco can yield high-quality visualizations and quantitative outcomes. Furthermore, scDisco has been validated using real datasets, affirming its proficiency in cell clustering quality, retaining batch-specific cell types and identifying condition-specific genes.

conclusionscDisco is an effective integration method based on variational autoencoders, which improves analytical tasks of reducing batch effects, cell clustering, retaining batch-specific cell types and identifying condition-specific genes.

Indexed as

LearningSingle-Cell Gene Expression AnalysisAlgorithmsCluster AnalysisGene Expression ProfilingRNASequence Analysis, RNASingle-Cell AnalysisRNACellular heterogeneityCondition domain adaptationDisentangled representation learningIntegrationScRNA-seqVariational autoencoder

Identifiers

PMID38493095
PMCPMC10944609

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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.