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Effective multi-modal clustering method via skip aggregation network for parallel scRNA-seq and scATAC-seq data.
Hu, Dayu; Liang, Ke; Dong, Zhibin; Wang, Jun; Zhao, Yawei; He, Kunlun.
Afiliação
  • Hu D; School of Computer, National University of Defense Technology, No. 109 Deya Road, 410073 Changsha, Hunan, China.
  • Liang K; School of Computer, National University of Defense Technology, No. 109 Deya Road, 410073 Changsha, Hunan, China.
  • Dong Z; School of Computer, National University of Defense Technology, No. 109 Deya Road, 410073 Changsha, Hunan, China.
  • Wang J; School of Computer, National University of Defense Technology, No. 109 Deya Road, 410073 Changsha, Hunan, China.
  • Zhao Y; Medical Big Data Research Center, Chinese PLA General Hospital, No. 28 Fuxing Road, 100853 Beijing, China.
  • He K; Medical Big Data Research Center, Chinese PLA General Hospital, No. 28 Fuxing Road, 100853 Beijing, China.
Brief Bioinform ; 25(2)2024 Jan 22.
Article em En | MEDLINE | ID: mdl-38493338
ABSTRACT
In recent years, there has been a growing trend in the realm of parallel clustering analysis for single-cell RNA-seq (scRNA) and single-cell Assay of Transposase Accessible Chromatin (scATAC) data. However, prevailing methods often treat these two data modalities as equals, neglecting the fact that the scRNA mode holds significantly richer information compared to the scATAC. This disregard hinders the model benefits from the insights derived from multiple modalities, compromising the overall clustering performance. To this end, we propose an effective multi-modal clustering model scEMC for parallel scRNA and Assay of Transposase Accessible Chromatin data. Concretely, we have devised a skip aggregation network to simultaneously learn global structural information among cells and integrate data from diverse modalities. To safeguard the quality of integrated cell representation against the influence stemming from sparse scATAC data, we connect the scRNA data with the aggregated representation via skip connection. Moreover, to effectively fit the real distribution of cells, we introduced a Zero Inflated Negative Binomial-based denoising autoencoder that accommodates corrupted data containing synthetic noise, concurrently integrating a joint optimization module that employs multiple losses. Extensive experiments serve to underscore the effectiveness of our model. This work contributes significantly to the ongoing exploration of cell subpopulations and tumor microenvironments, and the code of our work will be public at https//github.com/DayuHuu/scEMC.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromatina / RNA Citoplasmático Pequeno Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromatina / RNA Citoplasmático Pequeno Idioma: En Ano de publicação: 2024 Tipo de documento: Article