4.7 Article

Identification of cell-type-specific genes in multimodal single-cell data using deep neural network algorithm

期刊

COMPUTERS IN BIOLOGY AND MEDICINE
卷 166, 期 -, 页码 -

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.compbiomed.2023.107498

关键词

Bioinformatics; Multimodal single-cell study; Deep learning

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The emergence of single-cell RNA sequencing technology allows for simultaneous measurement of DNA, RNA, and protein in a single cell. The CITE-seq method enables the capture of RNA and surface protein expression simultaneously. In this study, CITE-seq datasets were analyzed to identify differentially expressed genes in seven cell types during bone marrow stem cell differentiation, and the relation between RNA and protein levels was predicted with a high score using a deep neural network model. Three cell-type-specific genes were identified in erythrocyte progenitor. This study provides valuable insights into stem cell differentiation in the bone marrow.
The emergence of single-cell RNA sequencing (scRNA-seq) technology makes it possible to measure DNA, RNA, and protein in a single cell. Cellular Indexing of Transcriptomes and Epitopes by sequencing (CITE-seq) is a powerful multimodal single-cell research innovation, allowing researchers to capture RNA and surface protein expression on the same cells. Currently, identification of cell-type-specific genes in CITE-seq data is still challenging. In this study, we obtained a set of CITE-seq datasets from Kaggle database, which included the sequencing dataset of seven cell types during bone marrow stem cell differentiation. We used Student's t-test to analyze these transcription RNAs and pick out 133 significantly differentially expressed genes (DEGs) among all cell types. Functional enrichment revealed that these DEGs were strongly associated with blood-related diseases, providing important insights into the cellular heterogeneity within bone marrow stem cells. The relation between RNA and protein levels was performed by deep neural network (DNN) model and achieved a high prediction score of 0.867. Based on their coefficients in the DNN model, three genes (LGALS1, CENPV, TRIM24) were identified as cell-type-specific genes in erythrocyte progenitor. Our works provide a novel perspective regarding the differentiation of stem cells in the bone marrow and provide valuable insights for further research in this field.

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