| 实验编号 | CRX105729 |
| 物种名称 | Camellia sinensis |
| 标题 | Camellia sinensis var. sinensis cv. Biyun PB02 |
| 项目编号 | PRJCA002071 |
| 样本编号 | SAMC126111 |
| 测序平台 | PacBio Sequel |
| 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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The SMRTbell template libraries were prepared following the standard protocol for long insert libraries according to the instructions. Genomic DNA was firstly sheared. The large fragments were enriched and enzymatically repaired and converted into the three SMRTbell template libraries. These fragments were ligated with hairpin adapters. The remaining damaged DNA fragments and those without adapters at both ends were eliminated by digestion with exonucleases. The resulting SMRTbell templates were selected by Blue Pippin electrophoresis and sequenced on a Sequel instrument. |
WGS |
GENOMIC |
unspecified |
SINGLE
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| 处理信息 |
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| 发布日期 | 2020-04-28 |
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| 测序反应 |
| Run编号 |
Run序列文件信息 |
| File name | File size (MB) |
|---|
| CRR130322 |
CRR130322.fastq.gz
|
1,567.93
|
|
| 提交者 | Wei Li (liweisdau@126.com) |
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| 所属单位 | South China Agricultural University |
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| 提交日期 | 2020-04-23 |
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