| 实验编号 | CRX637424 |
| 物种名称 | Bacteria |
| 标题 | pe-2-2 |
| 项目编号 | PRJCA015536 |
| 样本编号 | SAMC1153860 |
| 测序平台 | Illumina HiSeq 2500 |
| 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 DNA of sludge samples were extracted. Primers 515F (5’-GTGCCAGCMGCCGCGGTAA-3’) and 818R (5’-GGACTACHVGGGTWTCTAAT-3’) were used for 16S rRNA gene V4 region amplification. The PCR products with different barcodes were purified, quantified, and pooled tighter to construct the DNA library, and high throughput sequencing was performed on Illumina sequencing platform. |
AMPLICON |
OTHER |
PCR |
PAIRED
|
|
| 处理信息 |
Planned read length (bp) for mate 1: 250
Planned read length (bp) for mate 2: 250
|
| 发布日期 | 2023-03-16 |
|---|
| 测序反应 |
| Run编号 |
Run序列文件信息 |
| File name | File size (MB) |
|---|
| CRR711339 |
CRR711339_f1.fq.gz
CRR711339_r2.fq.gz
|
7.76
7.14
|
|
| 提交者 | Qiao Ma (xiaoma0556@qq.com) |
|---|
| 所属单位 | Dalian Maritime University |
|---|
| 提交日期 | 2023-03-16 |
|---|
