转录组
铬
前列腺癌
细胞
小RNA
计算生物学
信使核糖核酸
生物
RNA序列
核糖核酸
注释
遗传学
生物信息学
癌症
化学
基因
基因表达
有机化学
作者
Stefan Salcher,Isabel Heidegger,Gerold Untergasser,Georgios Fotakis,Alexandra Scheiber,Agnieszka Martowicz,Asma Noureen,Anne Krogsdam,Christoph Schatz,Georg Schäfer,Zlatko Trajanoski,Dominik Wolf,Sieghart Sopper,Andreas Pircher
出处
期刊:Heliyon
[Elsevier BV]
日期:2024-03-19
卷期号:10 (7): e28358-e28358
被引量:26
标识
DOI:10.1016/j.heliyon.2024.e28358
摘要
The development of single-cell omics tools has enabled scientists to study the tumor microenvironment (TME) in unprecedented detail. However, each of the different techniques may have its unique strengths and limitations. Here we directly compared two commercially available high-throughput single-cell RNA sequencing (scRNA-seq) technologies - droplet-based 10X Chromium vs. microwell-based BD Rhapsody - using paired samples from patients with localized prostate cancer (PCa) undergoing a radical prostatectomy. Although high technical consistency was observed in unraveling the whole transcriptome, the relative abundance of cell populations differed. Cells with low mRNA content such as T cells were underrepresented in the droplet-based system, at least partly due to lower RNA capture rates. In contrast, microwell-based scRNA-seq recovered less cells of epithelial origin. Moreover, we discovered platform-dependent variabilities in mRNA quantification and cell-type marker annotation. Overall, our study provides important information for selection of the appropriate scRNA-seq platform and for the interpretation of published results.
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