Evidence map›Paper›PMID 33602306›Full record

ArticleGenome biology2021

iMAP: integration of multiple single-cell datasets by adversarial paired transfer networks.

Dongfang Wang, Siyu Hou, Lei Zhang, Xiliang Wang, Baolin Liu, Zemin Zhang

Abstract read
In one paragraph

Article in Genome biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing 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

36 citing papers in PubMed.

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

6 authors.

Dongfang Wang *BIOPIC and School of Life Sciences, Peking University, Beijing, China. wangdf19@pku.edu.cn.
Siyu Hou *MOE Key Laboratory for Bioinformatics, BNRIST Bioinformatics Division, Department of Automation, Tsinghua University, Beijing, China.
Lei ZhangInstitute of Cancer Research, Shenzhen Bay Laboratory, Shenzhen, China.
Xiliang WangAnalytical Biosciences Limited, Beijing, China.
Baolin LiuBIOPIC and School of Life Sciences, Peking University, Beijing, China.
Zemin ZhangBIOPIC and School of Life Sciences, Peking University, Beijing, China. zemin@pku.edu.cn.ORCID 0000-0003-3789-6536

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The integration of single-cell RNA-sequencing datasets from multiple sources is critical for deciphering cell-to-cell heterogeneities and interactions in complex biological systems. We present a novel unsupervised batch effect removal framework, called iMAP, based on both deep autoencoders and generative adversarial networks. Compared with current methods, iMAP shows superior, robust, and scalable performance in terms of both reliably detecting the batch-specific cells and effectively mixing distributions of the batch-shared cell types. Applying iMAP to tumor microenvironment datasets from two platforms, Smart-seq2 and 10x Genomics, we find that iMAP can leverage the powers of both platforms to discover novel cell-cell interactions.

Indexed as

RNA-SeqSingle-Cell AnalysisAlgorithmsComputational BiologyDeep LearningGenomicsHumansOrgan SpecificityReproducibility of ResultsSequence Analysis, RNAData integrationDeep learningGANscRNA-seq

Identifiers

PMID33602306
PMCPMC7891139

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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.