生物
RNA序列
计算生物学
转录组
单细胞测序
大规模并行测序
cDNA文库
DNA测序
单细胞分析
遗传学
互补DNA
基因
细胞
基因表达
外显子组测序
表型
作者
Kedar Nath Natarajan,Zhichao Miao,Miaomiao Jiang,Xiaoyun Huang,Hongpo Zhou,Jiarui Xie,Chunqing Wang,Shishang Qin,Zhikun Zhao,Liang Wu,Naibo Yang,Bo Li,Yong Hou,Shiping Liu,Sarah A. Teichmann
出处
期刊:Genome Biology
[Springer Nature]
日期:2019-04-08
卷期号:20 (1)
被引量:104
标识
DOI:10.1186/s13059-019-1676-5
摘要
Single-cell RNA-seq technologies require library preparation prior to sequencing. Here, we present the first report to compare the cheaper BGISEQ-500 platform to the Illumina HiSeq platform for scRNA-seq. We generate a resource of 468 single cells and 1297 matched single cDNA samples, performing SMARTer and Smart-seq2 protocols on two cell lines with RNA spike-ins. We sequence these libraries on both platforms using single- and paired-end reads. The platforms have comparable sensitivity and accuracy in terms of quantification of gene expression, and low technical variability. Our study provides a standardized scRNA-seq resource to benchmark new scRNA-seq library preparation protocols and sequencing platforms.
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