| Library |
| Library name |
Construction protocol |
Strategy |
Source |
Selection |
Layout |
|
Qualified DNA fragmentation were carried out by Ultrasonic Processor, the length of insert fragment was approximately 350 bp. Then terminal repair, add base A, add sequence adapter, purification, PCR amplification were implemented to complete the 350 bp library preparation. Subsequently, preliminary quantitative by Qubit 2.0, library concentration was diluted to 1 ng/ul. Then library's insert size was verified by Agilent 2100, finally Q-PCR were implemented to ensure the effective quantitative concentrations of library. |
WGS |
GENOMIC |
unspecified |
PAIRED
|
|
