| Literature DB >> 31491452 |
Yiwen Zhou1, Hao Xu1, Haiyang Wu2, Haili Yu1, Peng Zhou2, Xin Qiu2, Zihan Zheng1, Qin Chen2, Fa Xu2, Gang Li3, Jianzhi Zhou4, Gang Cheng1, Wei He5, Liyun Zou6, Ying Wan7.
Abstract
High-throughput sequencing for transcriptome profiling is an increasingly accessible and important tool for biological research. However, accurate profiling of small cell populations remains challenging due to issues with gene detection sensitivity and experimental complexity. Here we describe a streamlined RNAseq protocol (EASY RNAseq) for sensitive transcriptome assessment starting from low amount of input materials. EASY RNAseq is technically robust enough for sequencing small pools of cells, recovering information on larger amounts of genes and with a more even expression distribution pattern than other commonly used methods. Application of EASY RNAseq to single-human embryos at the 8-cell stage led to detection of 70% of currently annotated protein-coding genes. This workflow may thus serve as a useful tool for sensitive interrogation of rare cell populations.Entities:
Keywords: RNAseq; T cells; embryo; low input; mRNA
Mesh:
Year: 2019 PMID: 31491452 DOI: 10.1016/j.jmb.2019.08.002
Source DB: PubMed Journal: J Mol Biol ISSN: 0022-2836 Impact factor: 5.469