| 实验编号 | CRX1576199 |
| 物种名称 | Berchemiella wilsonii |
| 外部数据库编号 |
: |
| 标题 | Ber_genome_DNBSEQ |
| 项目编号 | PRJCA037665 |
| 样本编号 | SAMC4889365 |
| 测序平台 | DNBSEQ-T7 |
| 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 |
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After confirming the quality of DNA sample, the Covaris ultrasound fragmentor was used to randomly break it apart. This was followed by terminal repair, A-tailing, sequencing adapter addition, purification, and PCR amplification to complete the whole library preparation process. After the construction of the library, Qubit 3.0 was used for preliminary quantification, and the library was diluted. Then Agilent 2100 was used to detect the inserted fragments of the library |
WGS |
GENOMIC |
PCR |
PAIRED
|
|
| 处理信息 |
Planned read length (bp) for mate 1: 150
Planned read length (bp) for mate 2: 150
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| 发布日期 | 2025-09-19 |
|---|
| 测序反应 |
| Run编号 |
Run序列文件信息 |
| File name | File size (MB) |
|---|
| CRR1703329 |
CRR1703329_r1.fq.gz
CRR1703329_r2.fq.gz
|
125,768.15
132,366.91
|
|
| 提交者 | jianghao pang (2062992008@qq.com) |
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| 所属单位 | Wuhan Botanical Garden, Chinese Academy of Sciences |
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| 提交日期 | 2025-03-25 |
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