| 实验编号 | CRX1334059 |
| 物种名称 | Orchidaceae |
| 标题 | Gastrodia elata_A_S1 |
| 项目编号 | PRJCA034717 |
| 样本编号 | SAMC4534265 |
| 测序平台 | Illumina NovaSeq 6000 |
| 建库信息 |
| 文库名称 |
文库构建方法 |
建库策略 |
样品来源 |
实验选择 |
文库布局 |
|
After the total RNA extracted from the sample was qualified, the eukaryotic mRNA was enriched by magnetic beads connected with Oligo(dT).
The extracted mRNA was divided into fragments randomly by Fragmentation Buffer.
A cDNA strand was synthesized using six-base Random hexamers based on the fragment mRNA template.
Buffer solution, dNTPs, RNaseH and DNA Polymerase I were then added to synthesize two-strand cDNA. |
RNA-Seq |
TRANSCRIPTOMIC |
PCR |
PAIRED
|
|
| 处理信息 |
Planned read length (bp) for mate 1: 150
Planned read length (bp) for mate 2: 150
|
| 发布日期 | 2025-01-10 |
| 测序反应 |
| Run编号 |
Run序列文件信息 |
| File name | File size (MB) |
| CRR1451618 |
CRR1451618_r1.fastq.gz
CRR1451618_r2.fastq.gz
|
1,121.66
1,192.11
|
|
| 提交者 | jie Liu (liujie6470@163.com) |
| 所属单位 | China Three Gorges University |
| 提交日期 | 2025-01-08 |