Multiplexed droplet single-cell RNA-sequencing using natural genetic variation
- PMID: 29227470
- PMCID: PMC5784859
- DOI: 10.1038/nbt.4042
"VSports手机版" Multiplexed droplet single-cell RNA-sequencing using natural genetic variation
Erratum in
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V体育平台登录 - Author Correction: Multiplexed droplet single-cell RNA-sequencing using natural genetic variation.Nat Biotechnol. 2020 Nov;38(11):1356. doi: 10.1038/s41587-020-0715-9. Nat Biotechnol. 2020. PMID: 33057163
Abstract
Droplet single-cell RNA-sequencing (dscRNA-seq) has enabled rapid, massively parallel profiling of transcriptomes. However, assessing differential expression across multiple individuals has been hampered by inefficient sample processing and technical batch effects. Here we describe a computational tool, demuxlet, that harnesses natural genetic variation to determine the sample identity of each droplet containing a single cell (singlet) and detect droplets containing two cells (doublets). These capabilities enable multiplexed dscRNA-seq experiments in which cells from unrelated individuals are pooled and captured at higher throughput than in standard workflows VSports手机版. Using simulated data, we show that 50 single-nucleotide polymorphisms (SNPs) per cell are sufficient to assign 97% of singlets and identify 92% of doublets in pools of up to 64 individuals. Given genotyping data for each of eight pooled samples, demuxlet correctly recovers the sample identity of >99% of singlets and identifies doublets at rates consistent with previous estimates. We apply demuxlet to assess cell-type-specific changes in gene expression in 8 pooled lupus patient samples treated with interferon (IFN)-β and perform eQTL analysis on 23 pooled samples. .
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"VSports注册入口" References
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- Nagano T, et al. Nature. 2013;502:59–64. - PMC (VSports) - PubMed
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- Patel AP, et al. Science. Vol. 344. American Association for the Advancement of Science; 2014. pp. 1396–1401. - PubMed
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