利用RECODE平台对单细胞数据进行全面降噪。

IF 4.5 Q1 BIOCHEMICAL RESEARCH METHODS
Yusuke Imoto
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引用次数: 0

摘要

单细胞测序能够对数千个单个细胞进行基因组和表观基因组分析,提供前所未有的生物学见解。然而,技术噪声和批处理效应模糊了高分辨率结构,阻碍了稀有细胞类型的检测和跨数据集的比较。为了全面解决这些挑战,本研究升级了RECODE,这是一种基于高维统计的单细胞RNA测序(RNA-seq)技术降噪工具,包括一个名为iRECODE的功能,可以同时降低技术和批量噪声。此外,RECODE的适用性扩展到多种单细胞模式,包括单细胞高通量染色体构象捕获(Hi-C)和空间转录组学。该算法最近的改进大大提高了精度和计算效率。因此,RECODE平台提供了一种强大而通用的降噪解决方案,可以跨转录组、表观基因组和空间域进行更准确的下游分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive noise reduction in single-cell data with the RECODE platform.

Single-cell sequencing enables genome- and epigenome-wide profiling of thousands of individual cells, offering unprecedented biological insights. However, technical noise and batch effects obscure high-resolution structures, hindering rare-cell-type detection and cross-dataset comparisons. To comprehensively address these challenges, this study upgrades RECODE, a high-dimensional statistics-based tool for technical noise reduction in single-cell RNA sequencing (RNA-seq), to include a function called iRECODE, which simultaneously reduces technical and batch noise. Further, RECODE's applicability is extended to diverse single-cell modalities, including single-cell high-throughput chromosome conformation capture (Hi-C) and spatial transcriptomics. Recent improvements in the algorithm have substantially enhanced both accuracy and computational efficiency. The RECODE platform thus provides a robust and versatile solution for noise mitigation, enabling more accurate downstream analyses across transcriptomic, epigenomic, and spatial domains.

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来源期刊
Cell Reports Methods
Cell Reports Methods Chemistry (General), Biochemistry, Genetics and Molecular Biology (General), Immunology and Microbiology (General)
CiteScore
3.80
自引率
0.00%
发文量
0
审稿时长
111 days
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