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.

01

Non-Invasive Prenatal Testing (NIPT)

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, including trisomy 21 and other common aneuploidies. Using a simple maternal blood sample, NIPT provides an accurate, non-invasive alternative to invasive prenatal diagnostic procedures.

Non-Invasive Prenatal Testing (NIPT)

Complete Workflow

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

Delivering accurate and reliable sequencing data for confident prenatal screening.

Flexible Throughput

Multiple output options eliminate sample batching and accommodate varying testing volumes.

Broad Compatibility

Compatible with mainstream NGS library preparation methods, enabling both routine and expanded NIPT applications.

02

Preimplantation Genetic Testing for Aneuploidy (PGT-A)

Preimplantation Genetic Testing for Aneuploidy (PGT-A) is an NGS-based genetic testing method performed on embryos generated through in vitro fertilization (IVF). By sequencing amplified embryonic DNA, PGT-A evaluates chromosome copy number across all 23 chromosome pairs, enabling the detection of whole-chromosome aneuploidies and large copy number variations (CNVs). The comprehensive assessment of chromosomal status supports the identification of euploid embryos for embryo selection prior to implantation.

Preimplantation Genetic Testing for Aneuploidy (PGT-A)

High Accuracy

Delivering reliable sequencing performance for confident embryo chromosome analysis.

Streamlined Workflow

Simplifying laboratory operations with an efficient PGT-A sequencing workflow.

Flexible Throughput

Scalable sequencing output accommodates laboratories with different testing volumes.

Reliable Analysis

Supporting stable and reproducible PGT-A data analysis for reproductive genetics and IVF laboratories.

X1 Bioinformatics Workstation

X1 Bioinformatics Workstation is an integrated bioinformatics solution, designed to streamline sequencing data analysis from raw data to application-ready reports. Featuring flexible hardware configurations and pre-built bioinformatics pipelines, it delivers plug-and-run, end-to-end data analysis for diverse laboratory throughput needs.

X1 requires no complicated deployment or professional bioinformatics setup, allowing one-click standardized analysis to cut hands-on work, shorten turnaround time, boost data security and deliver actionable sequencing results faster.

X1 Bioinformatics Workstation

Highlights

Versatile Bioinformatics

Supports multiple bioinformatics plugins for a wide range of analysis applications.

Secure Offline Operation

Runs reliably offline to help keep sensitive data secure and private.

Easy to Use

No complex command-line operations required, enabling streamlined analysis with minimal training.

Intelligent System Management

Real-time memory and storage monitoring with early warnings to help prevent capacity issues.