Evidence map›Paper›PMID 37308294›Full record

ArticleGenome research2023

Accurate integration of multiple heterogeneous single-cell RNA-seq data sets by learning contrastive biological variation.

Yang Zhou, Qiongyu Sheng, Jing Qi, Jiao Hua, Bo Yang, Lei Wan, Shuilin Jin

Abstract read
In one paragraph

Article in Genome research, 2023. 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

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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Integrating single-cell data with biological variables.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Single-Cell Hi-C Technologies and Computational Data Analysis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Review
  5. Review
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

7 authors.

Yang ZhouSchool of Mathematics, Harbin Institute of Technology, Harbin, Heilongjiang Province, China, 150001.
Qiongyu ShengSchool of Mathematics, Harbin Institute of Technology, Harbin, Heilongjiang Province, China, 150001.
Jing QiSchool of Mathematics, Harbin Institute of Technology, Harbin, Heilongjiang Province, China, 150001.
Jiao HuaSchool of Mathematics, Harbin Institute of Technology, Harbin, Heilongjiang Province, China, 150001.
Bo YangSchool of Mathematics, Harbin Institute of Technology, Harbin, Heilongjiang Province, China, 150001.
Lei WanSchool of Mathematics, Harbin Institute of Technology, Harbin, Heilongjiang Province, China, 150001.
Shuilin JinSchool of Mathematics, Harbin Institute of Technology, Harbin, Heilongjiang Province, China, 150001 jinsl@hit.edu.cn.ORCID 0000-0002-2318-432X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

For most biological and medical applications of single-cell transcriptomics, an integrative study of multiple heterogeneous single-cell RNA sequencing (scRNA-seq) data sets is crucial. However, present approaches are unable to integrate diverse data sets from various biological conditions effectively because of the confounding effects of biological and technical differences. We introduce single-cell integration (scInt), an integration method based on accurate, robust cell-cell similarity construction and unified contrastive biological variation learning from multiple scRNA-seq data sets. scInt provides a flexible and effective approach to transfer knowledge from the already integrated reference to the query. We show that scInt outperforms 10 other cutting-edge approaches using both simulated and real data sets, particularly in the case of complex experimental designs. Application of scInt to mouse developing tracheal epithelial data shows its ability to integrate development trajectories from different developmental stages. Furthermore, scInt successfully identifies functionally distinct condition-specific cell subpopulations in single-cell heterogeneous samples from a variety of biological conditions.

Indexed as

Single-Cell AnalysisSingle-Cell Gene Expression AnalysisAnimalsExome SequencingGene Expression ProfilingMiceSequence Analysis, RNA

Identifiers

PMID37308294
PMCPMC10317120

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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.