There are obvious differences in cDNA library construction between bacterial RNA-Seq and Eukaryotic RNA-Seq. Bacterial RNA-Seq workflow’s first step is selection of mRNA transcripts. Ribo-Zero ribosomal RNA reduction chemistry is used in place a poly-A tail selection which makes this method particularly suited for bacteria mRNA lack a poly-A tail. Following purification, the mRNA is fragmented into small pieces, and copied into first strand cDNA using reverse transcriptase and random primers. Strand specificity is achieved by replacing dTTP with dUTP in the Second Strand Marking Mix (SMM), followed by second strand cDNA synthesis. Through the use of strand-specific RNA-Seq, a more complete understanding of the transcriptome could be achieved, this has the potential to identify new levels of regulation of gene expression.
项目工作流程

样品要求:
测序服务策略:
HiSeq X十,150 PE,1~3 G/每个样品
MGI DNBSEQ-T7/DNBSEQ-G400
数据分析
无参考的成绩单
带参考的成绩单
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