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文库构建方法 |
建库策略 |
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文库布局 |
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Total RNA was isolated using RNeasy mini kit (Qiagen, Germany). Strand-specific libraries were prepared using the TruSeq® Stranded Total RNA Sample Preparation kit (Illumina, USA) following the manufacturer’s instructions. Ribosomal RNA was removed from total RNA using Ribo-Zero rRNA removal beads.Purified libraries were quantified by Qubit® 2.0 Fluorometer (Life Technologies, USA) and validated by Agilent 2100 bioanalyzer (Agilent Technologies, USA) to confirm the insert size and calculate the mole concentration. Cluster was generated by cBot with the library diluted to 10 pM and then were sequenced on the Illumina HiSeq 2500 (Illumina, USA). |
RNA-Seq |
TRANSCRIPTOMIC |
RANDOM |
PAIRED
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