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Overcoming Expressional Drop-outs in Lineage Reconstruction from Single-Cell RNA-Sequencing Data

机译:从单细胞RNA排序数据克服谱系重建中的表达辍学

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摘要

Single-cell lineage tracing provides crucial insights into the fates of individual cells. Single-cell RNA sequencing (scRNA-seq) is commonly applied in modern biomedical research, but genetics-based lineage tracing for scRNA-seq data is still unexplored. Variant calling from scRNA-seq data uniquely suffers from “expressional drop-outs,” including low expression and allelic bias in gene expression, which presents significant obstacles for lineage reconstruction. We introduce SClineager, which infers accurate evolutionary lineages from scRNA-seq data by borrowing information from related cells to overcome expressional drop-outs. We systematically validate SClineager and show that genetics-based lineage tracing is applicable for single-cell-sequencing studies of both tumor and non-tumor tissues using SClineager. Overall, our work provides a powerful tool that can be applied to scRNA-seq data to decipher the lineage histories of cells and that could address a missing opportunity to reveal valuable information from the large amounts of existing scRNA-seq data.
机译:单细胞谱系跟踪为单个细胞的命运提供了重要的洞察力。单细胞RNA测序(ScRNA-SEQ)通常应用于现代生物医学研究,但基于遗传的谱系追踪SCRNA-SEQ数据仍然是未开发的。来自ScRNA-SEQ数据的变体呼叫唯一地遭受“表达辍学”,包括基因表达中的低表达和等位基因偏压,这提出了谱系重建的重要障碍。我们介绍Sclineager,它通过借用相关细胞借用从相关细胞借用以克服表达的辍学来源的精确进化谱系。我们系统地验证了SclineAger,并表明基于遗传学的谱系跟踪适用于使用Scllineger的肿瘤和非肿瘤组织的单细胞排序研究。总的来说,我们的工作提供了一种强大的工具,可以应用于ScrNA-SEQ数据以破译细胞的谱系历史,这可能会解决从大量现有SCRNA-SEQ数据中揭示有价值信息的遗失机会。

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