Experiment information
Accession CRX038441
Organism Plutella xylostella
Title third
BioProject PRJCA001194
BioSample SAMC053462
Platform Illumina HiSeq X Ten
Library
Library name Construction protocol Strategy Source Selection Layout
Total RNA from these 10 samples (eggs, 1st larvae, 2nd larvae, 3rd larvae, 4th male larvae, 4th female larvae, male pupae, female pupae, male adults, female adults) were grinded in TRIzol regent on the dry ice, and then processed following the protocol of RNAeasy Mini Kit (manufacturer: Qiagen). To remove DNA, total RNA was treated with DNaseI (manufacturer: Qiagen). We used the Agilent 2100 with an RNA Integrity Number (RIN) value to assess the total RNA quality. RNA samples with RIN > 8 were used for following analyses. RNA-seq libraries were constructed using 20 µg total RNA from all samples (2 µg for each sample) following the protocol from ScriptSeq kit. Finally, Illumina HiSeq 2507 platform was used to generate the PE (Paired-end) reads. RNA-Seq TRANSCRIPTOMIC PolyA PAIRED
Processing Planned read length (bp) for mate 1: 151
Planned read length (bp) for mate 2: 151
Insert size (bp): 400
Release date2019-01-20
Run
Run accession Run data file information
File nameFile size (MB)
CRR043112 CRR043112_f1.fastq.gz
CRR043112_r2.fastq.gz
3,062.11
3,625.6
Submitterlin jing (lolyemily@163.com)
OrganizationBeijing Institute of Genomics, Chinese Academy of Sciences
Date submitted2019-01-10