Evidence map›Paper›PMID 33767393›Full record

ArticleNature biotechnology2021

Robust integration of multiple single-cell RNA sequencing datasets using a single reference space.

Yang Liu, Tao Wang, Bin Zhou, Deyou Zheng

Abstract read
In one paragraph

Article in Nature biotechnology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing 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

30 citing papers in PubMed.

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  11. Deep Batch Integration and Denoise of Single-Cell RNA-Seq Data.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
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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.

Yang LiuDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
Tao WangDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
Bin ZhouDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA.
Deyou ZhengDepartment of Genetics, Albert Einstein College of Medicine, Bronx, NY, USA. deyou.zheng@einsteinmed.org.ORCID http://orcid.org/0000-0003-4354-5337

Funding

Project 2: Genetic Mechanisms of Non-syndromic Congenital Cardiac DefectsP01HD070454 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI GOLDMUNTZ, ELIZABETH · 2011 to 2020
$14.0M
Molecular and Cellular Mechanisms in Coronary Artery Development and AnomaliesR01HL133120 · NHLBI · UNIVERSITY OF CHICAGO · PI BIN ZHOU · 2016 to 2026
$4.6M
Cell fate choices by Tbx1 in forming the mammalian heartR01HL153920 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI BERNICE E MORROW, Deyou Zheng · 2020 to 2026
$4.0M
Single Cell RNA-seq to Identify Endocardial Ontogenic Factors for the HeartR21HD092944 · NICHD · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI ZHENG, DEYOU, ZHOU, BIN · 2018 to 2019
$459k
NHLBI NIH HHS R01 HL133120NHLBI NIH HHS R01 HL153920NICHD NIH HHS P01 HD070454NICHD NIH HHS R21 HD092944
6 · The paper itself

Abstract

In many biological applications of single-cell RNA sequencing (scRNA-seq), an integrated analysis of data from multiple batches or studies is necessary. Current methods typically achieve integration using shared cell types or covariance correlation between datasets, which can distort biological signals. Here we introduce an algorithm that uses the gene eigenvectors from a reference dataset to establish a global frame for integration. Using simulated and real datasets, we demonstrate that this approach, called Reference Principal Component Integration (RPCI), consistently outperforms other methods by multiple metrics, with clear advantages in preserving genuine cross-sample gene expression differences in matching cell types, such as those present in cells at distinct developmental stages or in perturbated versus control studies. Moreover, RPCI maintains this robust performance when multiple datasets are integrated. Finally, we applied RPCI to scRNA-seq data for mouse gut endoderm development and revealed temporal emergence of genetic programs helping establish the anterior-posterior axis in visceral endoderm.

Indexed as

Computer SimulationDatabases, FactualSingle-Cell AnalysisBase SequenceGene DeletionHumansModels, BiologicalSequence Analysis, RNA

Identifiers

PMID33767393
PMCPMC8456427

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Registered trials

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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.