| Accession | CRX165654 |
| Organism | Bacteria |
| Title | M371_16S |
| BioProject | PRJCA003568 |
| BioSample | SAMC250442 |
| Platform | Illumina MiSeq |
| Library |
| Library name |
Construction protocol |
Strategy |
Source |
Selection |
Layout |
|
DNA was extracted using a MagNA Pure LC 2.0 system and a MagNA Pure LC Total NA Isolation kit in accordance with the manufacturer’s instructions and quantified using a QuantiT PicoGreen dsDNA Assay kit. PCR amplification of the V3-V4 region was performed with the following primers containing Illumina adapter sequences and dual-index barcodes to tag each sample. The amplicon sequencing libraries were constructed in accordance with the 16S Metagenomic Sequencing Library Preparation. |
AMPLICON |
GENOMIC |
PCR |
PAIRED
|
|
| Processing |
Planned read length (bp) for mate 1: 250
Planned read length (bp) for mate 2: 250
|
| Release date | 2021-05-13 |
|---|
| Run |
| Run accession |
Run data file information |
| File name | File size (MB) |
|---|
| CRR193531 |
CRR193531_f1.fq.gz
CRR193531_r2.fq.gz
|
2.54
2.79
|
|
| Submitter | Jiarui Li (li.jiarui@ccmu.edu.cn) |
|---|
| Organization | Beijing Ditan Hospital, Capital Medical University |
|---|
| Submitted date | 2020-09-30 |
|---|
