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splatPop:模拟群体规模单细胞 RNA 测序数据。

splatPop: simulating population scale single-cell RNA sequencing data.

机构信息

St. Vincent's Institute of Medical Research, 9 Princes Street, Fitzroy, 3065, VIC, Australia.

University of Melbourne, Royal Parade, Parkville, 3010, VIC, Australia.

出版信息

Genome Biol. 2021 Dec 15;22(1):341. doi: 10.1186/s13059-021-02546-1.

DOI:10.1186/s13059-021-02546-1
PMID:34911537
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8672480/
Abstract

Population-scale single-cell RNA sequencing (scRNA-seq) is now viable, enabling finer resolution functional genomics studies and leading to a rush to adapt bulk methods and develop new single-cell-specific methods to perform these studies. Simulations are useful for developing, testing, and benchmarking methods but current scRNA-seq simulation frameworks do not simulate population-scale data with genetic effects. Here, we present splatPop, a model for flexible, reproducible, and well-documented simulation of population-scale scRNA-seq data with known expression quantitative trait loci. splatPop can also simulate complex batch, cell group, and conditional effects between individuals from different cohorts as well as genetically-driven co-expression.

摘要

现在,基于人群的单细胞 RNA 测序(scRNA-seq)已经可行,这使得更精细的功能基因组学研究成为可能,并促使人们急于采用批量方法并开发新的单细胞特异性方法来进行这些研究。模拟在开发、测试和基准测试方法方面很有用,但目前的 scRNA-seq 模拟框架不能模拟具有遗传效应的基于人群的数据。在这里,我们提出了 splatPop,这是一种用于灵活、可重复和记录良好的基于人群的 scRNA-seq 数据模拟的模型,这些数据具有已知的表达数量性状基因座。splatPop 还可以模拟来自不同队列的个体之间的复杂批量、细胞群和条件效应,以及遗传驱动的共表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5097/8672480/668db659e102/13059_2021_2546_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5097/8672480/809bbefe27a9/13059_2021_2546_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5097/8672480/43eb6b4b76ea/13059_2021_2546_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5097/8672480/bc09b299a281/13059_2021_2546_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5097/8672480/e55fbb4da8f2/13059_2021_2546_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5097/8672480/668db659e102/13059_2021_2546_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5097/8672480/809bbefe27a9/13059_2021_2546_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5097/8672480/43eb6b4b76ea/13059_2021_2546_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5097/8672480/bc09b299a281/13059_2021_2546_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5097/8672480/e55fbb4da8f2/13059_2021_2546_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5097/8672480/668db659e102/13059_2021_2546_Fig5_HTML.jpg

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Scater: pre-processing, quality control, normalization and visualization of single-cell RNA-seq data in R.Scater:R语言中单细胞RNA测序数据的预处理、质量控制、标准化和可视化
Bioinformatics. 2017 Apr 15;33(8):1179-1186. doi: 10.1093/bioinformatics/btw777.
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A step-by-step workflow for low-level analysis of single-cell RNA-seq data with Bioconductor.使用Bioconductor进行单细胞RNA测序数据低级分析的逐步工作流程。
F1000Res. 2016 Aug 31;5:2122. doi: 10.12688/f1000research.9501.2. eCollection 2016.
ti-scMR:基于轨迹推断的动态单细胞孟德尔随机化识别表型差异背后的因果基因。
NAR Genom Bioinform. 2025 Jul 4;7(3):lqaf082. doi: 10.1093/nargab/lqaf082. eCollection 2025 Sep.
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scMetaIntegrator: a meta-analysis approach to paired single-cell differential expression analysis.scMetaIntegrator:一种用于配对单细胞差异表达分析的荟萃分析方法。
bioRxiv. 2025 Jun 8:2025.06.04.657898. doi: 10.1101/2025.06.04.657898.
5
Explainable deep neural networks for predicting sample phenotypes from single-cell transcriptomics.用于从单细胞转录组学预测样本表型的可解释深度神经网络。
Brief Bioinform. 2024 Nov 22;26(1). doi: 10.1093/bib/bbae673.
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scCTS: identifying the cell type-specific marker genes from population-level single-cell RNA-seq.scCTS:从群体水平的单细胞 RNA-seq 中识别细胞类型特异性标记基因。
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Nat Biotechnol. 2024 Sep 23. doi: 10.1038/s41587-024-02411-z.
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