From DNA extraction to tertiary analysis, we take care of the whole process and offer the most professional genome sequencing service to our clients.
From DNA extraction to tertiary analysis, we take care of the whole process and offer the most professional genome sequencing service to our clients.
We provide both short-read and long-read WGS to our clients.
Region : Whole genome
Depth : 30X
Read length: 151bp
Cover : SNPs, Indels, and Structure Variance
Ideal for PRS, disease studies, population genetics, or clinical practice.
Region : Whole genome
Depth : 30X
Read length: >1000bp
Cover : SNPs, Indels, Structure Variance, Repetitive Sequence, Haplotype Phasing, and De Novo Genome Assembly.
Most accurate and particularly suited for complex structural variants studies or De Novo Genome Assembly.
We provide not only WES but also the option of adding lcWGS (Low coverage WGS) to our clients with our proprietary integrated WES-lcWGS library construction method.
Region : Whole exome
Depth : 100X~200X
Read length: 151bp
Cover : SNPs, Indels and Structure Variance in protein coding region
Cost-effective alternative to WGS in clinical practice.
Region : Whole genome
Depth : 30X
Read length: 151bp
Cover : SNPs, Indels, Structure Variance and PRS.
Cost-effective alternative to WGS in PRS or research.