| 实验编号 | CRX203497 |
| 物种名称 | Microhyla fissipes |
| 标题 | L6-3 |
| 项目编号 | PRJCA004230 |
| 样本编号 | SAMC308924 |
| 测序平台 | Illumina HiSeq 4000 |
| 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 |
|
The library fragments were purified with AMPure XP system. Then the cDNA was amplified by PCR with aPhusion High-Fidelity DNA polymerase, universal PCR primers andIndex (X) primer. The PCR products were purified (AMPure XP system)and cDNA libraries were generated according to the manufacturer's instructions.After cluster generation, the libraries were sequenced on an IlluminaHiSeq 4032 platform, and paired-end reads were generated. |
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 | 2023-01-01 |
|---|
| 测序反应 |
| Run编号 |
Run序列文件信息 |
| File name | File size (MB) |
|---|
| CRR241838 |
CRR241838_f1.fq.gz
CRR241838_r2.fq.gz
|
1,442.12
1,522.56
|
|
| 提交者 | Liming Chang (changliming16@outlook.com) |
|---|
| 所属单位 | Chengdu Institute of Biology, Chinese Academy of Sciences |
|---|
| 提交日期 | 2021-01-13 |
|---|
