The whole genome sequence of the genome means the entire genome is read and analysed, providing the most detailed genetic variation information.
The first household genome map was completed by Genephenomics and various fauna-flora genes such as whales and tigers were successfully decrypted.
De novo sequencing is commonly achieved without prior knowledge of the sequencing. De novo sequencing has proven successful in confirming and expanding upon consequences from database searches, providing splendid assets for knowledge of species.
Some of the most important information obtained through the re-sequencing of the genome DNA of an organism are the human genetic variations, such as single nucleotide polymorphism(SNP), copy number variation(CNV), and structural variation(SV)
Sequencing Platforms
- NovaSeq 6000
- NextSeq 500, MiSeq
- PacBio RS II, PacBio Sequel
Service overview
- SNV/Indels
- Structure Variation
- Copy Number Variation
- Trio Analysis
