计算生物学
大规模并行测序
RNA序列
单细胞测序
Illumina染料测序
DNA测序
转录组
水准点(测量)
计算机科学
深度测序
cDNA文库
生物
互补DNA
基因
遗传学
基因表达
基因组
突变
大地测量学
地理
外显子组测序
作者
Kedar Nath Natarajan,Zhichao Miao,Miaomiao Jiang,Xiaoyun Huang,Hongpo Zhou,Jiarui Xie,Chunqing Wang,Shishang Qin,Zhikun Zhao,Liang Wu,Bo Li,Yong Hou,Shiping Liu,Sarah A. Teichmann
摘要
Abstract All single-cell RNA-seq protocols and technologies require library preparation prior to sequencing on a platform such as Illumina. Here, we present the first report to utilize the BGISEQ-500 platform for scRNA-seq, and compare the sensitivity and accuracy to Illumina sequencing. We generate a scRNA-seq resource of 468 unique single-cells and 1,297 matched single cDNA samples, performing SMARTer and Smart-seq2 protocols on mESCs and K562 cells with RNA spike-ins. We sequence these libraries on both BGISEQ-500 and Illumina HiSeq platforms using single- and paired-end reads. The two platforms have comparable sensitivity and accuracy in terms of quantification of gene expression, and low technical variability. Our study provides a standardised scRNA-seq resource to benchmark new scRNA-seq library preparation protocols and sequencing platforms.
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