Library |
Library name |
Construction protocol |
Strategy |
Source |
Selection |
Layout |
hifi |
The genomic library for second-generation short-read sequencing of the samples was constructed as follows: Firstly, high-quality genomic DNA was randomly sheared using a Covaris sonicator (Covaris, USA). Next, the TruSeq Nano DNA HT Library Preparation Kit (Illumina, USA) was utilized to create an Illumina sequencing library with a target insert size of 350 bp. Finally, the purified library was loaded onto the Illumina NovaSeq 6000 platform for sequencing. |
WGS |
GENOMIC |
unspecified |
SINGLE
|
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