Evidence map›Paper›PMID 38267858›Full record

ArticleBMC bioinformatics2024

InClust+: the deep generative framework with mask modules for multimodal data integration, imputation, and cross-modal generation.

Lifei Wang, Rui Nie, Xuexia Miao, Yankai Cai, Anqi Wang, Hanwen Zhang, Jiang Zhang, Jun Cai

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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 5 papers.

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5citing papers in PubMed
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5 citing papers in PubMed.

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5 · Who and what money

Authors and funding

8 authors.

Lifei Wang *Shulan (Hangzhou) Hospital, Affiliated to Zhejiang Shuren University Shulan International Medical College, Hangzhou, China. wanglf1020@gmail.com.
Rui Nie *China National Center for Bioinformation, Beijing, China.
Xuexia MiaoChina National Center for Bioinformation, Beijing, China.
Yankai CaiSchool of Economic and Management, China University of Geoscience, Wuhan, China.
Anqi WangShulan (Hangzhou) Hospital, Affiliated to Zhejiang Shuren University Shulan International Medical College, Hangzhou, China.
Hanwen ZhangShulan (Hangzhou) Hospital, Affiliated to Zhejiang Shuren University Shulan International Medical College, Hangzhou, China.
Jiang ZhangSchool of Systems Science, Beijing Normal University, Beijing, 100875, China. zhangjiang@bnu.edu.cn.
Jun CaiChina National Center for Bioinformation, Beijing, China. juncai@big.ac.cn.

Funding

National Key Research and Development Program of China 2021YFF1200904National Natural Science Foundation of China 61673070
6 · The paper itself

Abstract

backgroundWith the development of single-cell technology, many cell traits can be measured. Furthermore, the multi-omics profiling technology could jointly measure two or more traits in a single cell simultaneously. In order to process the various data accumulated rapidly, computational methods for multimodal data integration are needed.

resultsHere, we present inClust+, a deep generative framework for the multi-omics. It's built on previous inClust that is specific for transcriptome data, and augmented with two mask modules designed for multimodal data processing: an input-mask module in front of the encoder and an output-mask module behind the decoder. InClust+ was first used to integrate scRNA-seq and MERFISH data from similar cell populations, and to impute MERFISH data based on scRNA-seq data. Then, inClust+ was shown to have the capability to integrate the multimodal data (e.g. tri-modal data with gene expression, chromatin accessibility and protein abundance) with batch effect. Finally, inClust+ was used to integrate an unlabeled monomodal scRNA-seq dataset and two labeled multimodal CITE-seq datasets, transfer labels from CITE-seq datasets to scRNA-seq dataset, and generate the missing modality of protein abundance in monomodal scRNA-seq data. In the above examples, the performance of inClust+ is better than or comparable to the most recent tools in the corresponding task.

conclusionsThe inClust+ is a suitable framework for handling multimodal data. Meanwhile, the successful implementation of mask in inClust+ means that it can be applied to other deep learning methods with similar encoder-decoder architecture to broaden the application scope of these models.

Indexed as

ChromatinTranscriptomePhenotypeChromatinCross-modal generationCross-modal imputationData integrationDeep generative framework with mask modulesMulti-omics

Identifiers

PMID38267858
PMCPMC10809631

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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.