Instrument: Illumina HiSeq 2000
Strategy: EST
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Messenger RNA (mRNA) was isolated using the Dynabeads mRNA Purification Kit (Invitrogen, Carlsbad Ca. USA) and then sheared using divalent cations at 72*C. These cleaved RNA fragments were transcribed into first-strand cDNA using SuperScript™II Reverse Transcriptase (Invitrogen, Carlsbad Ca. USA) and N6 primer (IDT). The second-strand cDNA was subsequently synthesized using RNase H (Invitrogen, Carlsbad Ca. USA) and DNA polymerase I (Invitrogen, Shanghai China). The double-stranded cDNA then underwent end-repair, a single ‘A’ base addition, adapter ligation, and size selection on anagarose gel (250 * 20 bp). At last, the product was indexed and PCR amplified to finalize the library prepration for the paired-end cDNA.