| Library |
| Library name |
Construction protocol |
Strategy |
Source |
Selection |
Layout |
|
A total amount of 1.5µg DNA per sample was used as input material for the DNA sample preparations. Sequencing libraries were generated using Truseq Nano DNA HT Sample preparation Kit (Illumina USA) following manufacturer’s recommendations and index codes were added to attribute sequences to each sample. Briefly, the DNA sample was fragmented by sonication to a size of 350bp, then DNA fragments were end polished, A-tailed, and ligated with the full-length adapter for Illumina sequencing with further PCR amplification. At last, PCR products were purified (AMPure XP system) and libraries were analyzed for size distribution by Agilent2100 Bioanalyzer and quantified using real-time PCR. The qualified libraries were sequenced on MGISEQ-2000 platform. |
WGS |
GENOMIC |
PCR |
PAIRED
|
|
