Molecular Medicine and Gene Therapy, Wallenberg Centre for Molecular Medicine, Lund Stem Cell Center, Lund University, Lund, Sweden.
Department of Cell and Molecular Biology, Karolinska Institute, Stockholm, Sweden.
Life Sci Alliance. 2023 May 17;6(8). doi: 10.26508/lsa.202301979. Print 2023 Aug.
Single-cell sequencing (sc-seq) provides a species agnostic tool to study cellular processes. However, these technologies are expensive and require sufficient cell quantities and biological replicates to avoid artifactual results. An option to address these problems is pooling cells from multiple individuals into one sc-seq library. In humans, genotype-based computational separation (i.e., demultiplexing) of pooled sc-seq samples is common. This approach would be instrumental for studying non-isogenic model organisms. We set out to determine whether genotype-based demultiplexing could be more broadly applied among species ranging from zebrafish to non-human primates. Using such non-isogenic species, we benchmark genotype-based demultiplexing of pooled sc-seq datasets against various ground truths. We demonstrate that genotype-based demultiplexing of pooled sc-seq samples can be used with confidence in several non-isogenic model organisms and uncover limitations of this method. Importantly, the only genomic resource required for this approach is sc-seq data and a de novo transcriptome. The incorporation of pooling into sc-seq study designs will decrease cost while simultaneously increasing the reproducibility and experimental options in non-isogenic model organisms.
单细胞测序 (sc-seq) 提供了一种通用的工具,可以用于研究细胞过程。然而,这些技术昂贵,需要足够的细胞数量和生物学重复,以避免人为的结果。解决这些问题的一种选择是将来自多个个体的细胞汇集到一个 sc-seq 文库中。在人类中,基于基因型的计算分离(即解复用)是常见的。这种方法对于研究非同源模型生物将是非常有用的。我们着手确定基于基因型的解复用是否可以更广泛地应用于从斑马鱼到非人类灵长类动物等不同物种。使用这些非同源物种,我们根据各种真实情况来评估基于基因型的汇集 sc-seq 数据集的解复用。我们证明,基于基因型的汇集 sc-seq 样本的解复用可以在几种非同源模型生物中自信地使用,并揭示了这种方法的局限性。重要的是,这种方法只需要 sc-seq 数据和从头转录组作为基因组资源。将汇集纳入 sc-seq 研究设计将降低成本,同时提高非同源模型生物的可重复性和实验选择。