Gan Huaiyan, Feng Tieshan, Wu Yuqian, Liu Chun, Xia Qingyou, Cheng Tingcai
State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400716, China.
Data Brief. 2017 Oct 18;15:709-711. doi: 10.1016/j.dib.2017.10.028. eCollection 2017 Dec.
Circular transcriptome sequencing of the middle silk gland (MSG) and posterior silk gland (PSG) in the are presented. The middle silk gland and posterior silk gland were collected from the third day of fifth-instar larvae. The circular RNAs enriched by using RNase R to degrade the linear RNA molecules, and circular RNA sequencing (circRNA-seq) was performed using an Illumina Hiseq. 2500 sequencing platform. Samples are described in the SRA portal (SRP100385) and FASTQ files have been deposited in Sequence Read Archive (accession numbers: SRX2577343 and SRX2577342). The interpretation of these data is presented in the following research article: "Identification of circular RNA in the silk gland" [1] (Gan et al., 2017).
本文展示了家蚕中丝腺(MSG)和后丝腺(PSG)的环状转录组测序结果。中丝腺和后丝腺取自五龄幼虫的第三天。使用RNase R降解线性RNA分子来富集环状RNA,并使用Illumina Hiseq. 2500测序平台进行环状RNA测序(circRNA-seq)。样本在SRA数据库(SRP100385)中有所描述,FASTQ文件已存入序列读取存档库(登录号:SRX2577343和SRX2577342)。这些数据的解读发表于以下研究文章:《家蚕丝腺中环状RNA的鉴定》[1](Gan等人,2017年)。