Life Sciences

From DNA extraction to tertiary analysis, we take care of the whole process and offer the most professional genome sequencing service to our clients.

Our Services

01

WGS (Whole Genome Sequencing)

We provide both short-read and long-read WGS to our clients.

Short read WGS

Short read WGS

Short read WGS (Next Generation Sequencing) has been widely used in research purposes for decades and is getting into clinical use due to the gradual cost reduction nowadays.
icon Region : Whole genome
icon Depth : 30X
icon Read length: 151bp
icon Cover : SNPs, Indels, and Structure Variance
icon Ideal for PRS, disease studies, population genetics, or clinical practice.
Long read WGS

Long read WGS

Long read WGS (Third Generation sequencing) offers improved accuracy for complex variant detection, like repetitive sequences and structural variants, and haplotype phasing. It’s currently used for research purposes due to the high cost.
icon Region : Whole genome
icon Depth : 30X
icon Read length: >1000bp
icon Cover : SNPs, Indels, Structure Variance, Repetitive Sequence, Haplotype Phasing, and De Novo Genome Assembly.
icon Most accurate and particularly suited for complex structural variants studies or De Novo Genome Assembly.
02

WES (Whole Exome Sequencing) & lcWGS (Low Coverage WGS)

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.

WES

WES

Whole Exome Sequencing is widely used in both research and clinical because it’s a cost-efficient method to have deeper sequence coverage of the exome, the protein coding region.
icon Region : Whole exome
icon Depth : 100X~200X
icon Read length: 151bp
icon Cover : SNPs, Indels and Structure Variance in protein coding region
icon Cost-effective alternative to WGS in clinical practice.
WES + lcWGS

WES + lcWGS

WES + lcWGS is a package that combines WES and low coverage WGS (WGS with only 2-3X depth compared to traditional 30X depth). This package offers our clients a lower-budget option compared to WGS to discover the whole genome.
icon Region : Whole genome
icon Depth : 30X
icon Read length: 151bp
icon Cover : SNPs, Indels, Structure Variance and PRS.
icon Cost-effective alternative to WGS in PRS or research.

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