Department of Medical Biology, Faculty of Medicine, University of Szeged, Szeged 6720, Hungary.
Department of Genetics, School of Medicine, Stanford University, Stanford, California 94305, USA.
Sci Data. 2018 Jun 19;5:180119. doi: 10.1038/sdata.2018.119.
Pseudorabies virus (PRV) is an alphaherpesvirus of swine. PRV has a large double-stranded DNA genome and, as the latest investigations have revealed, a very complex transcriptome. Here, we present a large RNA-Seq dataset, derived from both short- and long-read sequencing. The dataset contains 1.3 million 100 bp paired-end reads that were obtained from the Illumina random-primed libraries, as well as 10 million 50 bp single-end reads generated by the Illumina polyA-seq. The Pacific Biosciences RSII non-amplified method yielded 57,021 reads of inserts (ROIs) aligned to the viral genome, the amplified method resulted in 158,396 PRV-specific ROIs, while we obtained 12,555 ROIs using the Sequel platform. The Oxford Nanopore's MinION device generated 44,006 reads using their regular cDNA-sequencing method, whereas 29,832 and 120,394 reads were produced by using the direct RNA-sequencing and the Cap-selection protocols, respectively. The raw reads were aligned to the PRV reference genome (KJ717942.1). Our provided dataset can be used to compare different sequencing approaches, library preparation methods, as well as for validation and testing bioinformatic pipelines.
伪狂犬病病毒(PRV)是一种猪的α疱疹病毒。PRV 具有一个大的双链 DNA 基因组,正如最新的研究揭示的那样,它具有一个非常复杂的转录组。在这里,我们提供了一个大型的 RNA-Seq 数据集,源自短读和长读测序。该数据集包含 130 万个 100bp 配对末端读取,这些读取是从 Illumina 随机引物文库中获得的,以及 1000 万个 50bp 单端读取,这些读取是由 Illumina polyA-seq 生成的。Pacific Biosciences RSII 非扩增方法产生了 57021 个与病毒基因组对齐的插入物(ROI)reads,扩增方法产生了 158396 个 PRV 特异性 ROI,而我们使用 Sequel 平台获得了 12555 个 ROI。Oxford Nanopore 的 MinION 设备使用其常规 cDNA 测序方法生成了 44006 个reads,而分别使用直接 RNA-seq 和 Cap-selection 协议生成了 29832 和 120394 个 reads。原始reads 被映射到 PRV 参考基因组(KJ717942.1)上。我们提供的数据集可用于比较不同的测序方法、文库制备方法,以及用于验证和测试生物信息学管道。