Focus Areas

Focus Areas

Focus Areas

Reliable, flexible sequencing solutions across reproductive health, pathogen detection, and genetic disease.

01

Reproductive Health: NIPT & PGT-A

Reproductive health applications increasingly rely on next-generation sequencing (NGS) to support prenatal screening and assisted reproductive technologies, enabling non-invasive or minimally invasive testing with reduced procedural risks, while delivering high accuracy, efficiency, and scalability.

Reproductive Health: NIPT & PGT-A

Non-Invasive Prenatal Testing (NIPT) is an NGS-based screening method that analyzes cell-free fetal DNA (cfDNA) in maternal plasma to assess the risk of chromosomal aneuploidies, while PGT-A evaluates chromosome copy number in IVF embryos to support embryo selection.

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Supporting the entire NIPT workflow from library preparation to sequencing, enabling non-invasive, low-risk prenatal screening while minimizing procedure-related infection risks.

High-quality data for confident prenatal screening

PGT-A analysis of all 23 chromosome pairs

Flexible throughput for varying testing volumes

02

Pathogen Detection: mNGS & tNGS

mNGS and tNGS support infectious disease research and clinical testing through complementary approaches, enabling broad, unbiased pathogen detection or targeted detection of clinically relevant pathogens with high sensitivity and accuracy.

Pathogen Detection: mNGS & tNGS

mNGS detects bacteria, viruses, fungi, and parasites without prior assumptions, while tNGS focuses sequencing on predefined panels of key pathogens associated with different infection sites, along with relevant resistance markers.

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Metagenomics sequencing (mNGS)

Broad-spectrum detection of bacteria, viruses, fungi, and parasites

Targeted panels for clinically relevant pathogens

Flexible throughput with rapid turnaround

03

Genetic Disease: WES & WGS

Next-generation sequencing (NGS) has transformed genetic disease research and clinical diagnostics by enabling comprehensive analysis of the human genome.

Genetic Disease: WES & WGS

WES focuses on protein-coding regions for efficient and cost-effective variant detection, while WGS provides comprehensive coverage of the entire genome, capturing variants across both coding and non-coding regions.

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Whole exome sequencing for coding variants

Whole genome sequencing for genome-wide variation

Uniform coverage and high-accuracy variant detection

Scalable throughput from individual samples to large studies