Transcriptome-wide survey of pseudorabies virus using next- and third-generation sequencing platforms

被引:19
|
作者
Tombacz, Dora [1 ]
Sharon, Donald [2 ]
Szucs, Attila [1 ]
Moldovan, Norbert [1 ]
Snyder, Michael [2 ]
Boldogkoi, Zsolt [1 ]
机构
[1] Univ Szeged, Dept Med Biol, Fac Med, H-6720 Szeged, Hungary
[2] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
关键词
IMMUNIZATION; ALIGNMENT; PIGS; RNA;
D O I
10.1038/sdata.2018.119
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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. [GRAPHICS] .
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页数:13
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