Experiment information
Accession CRX180805
Organism Phyllostachys edulis
Title M1
BioProject PRJCA003853
BioSample SAMC271313
Platform BGISEQ-500
Library
Library name Construction protocol Strategy Source Selection Layout
Oligo(dT)-attached magnetic beads were used to purified mRNA. Purified mRNA was fragmented into small pieces with fragment buffer at appropriate temperature. Then First-strand cDNA was generated using random hexamer-primed reverse transcription, followed by a second-strand cDNA synthesis. afterwards, A-Tailing Mix and RNA Index Adapters were added by incubating to end repair. The cDNA fragments obtained from previous step were amplified by PCR, and products were purified by Ampure XP Beads, then dissolved in EB solution. The product was validated on the Agilent Technologies 2100 bioanalyzer for quality control. The double stranded PCR products from previous step were heated denatured and circularized by the splint oligo sequence to get the final library. The single strand circle DNA (ssCir DNA) was formatted as the final library. The final library was amplified with phi29 to make DNA nanoball (DNB) which had more than 300 copies of one molecule, DNBs were loaded into the patterned nanoarray and single end 50 bases reads were generated on BGIseq500 platform. RNA-Seq TRANSCRIPTOMIC PolyA SINGLE
Processing Planned read length (bp): 50
Release date2021-02-19
Run
Run accession Run data file information
File nameFile size (MB)
CRR213452 CRR213452.bam 4,783
SubmitterYan Xiang (xiangyanahau@sina.com)
OrganizationAnhui Agricultural University
Date submitted2020-11-11