Genetic Disease IVD Solutions

Genetic diseases are health problems caused by genomic abnormalities. Their diagnosis typically requires genetic testing to identify specific gene mutations. As a supplier of in vitro diagnostic (IVD) products, Alta DiagnoTech provides professional institutions with advanced and comprehensive genetic disease testing solutions to ensure timely and accurate diagnostic support.

Overview of Genetic Diseases

Genetic disease is a disease that is passed on genetically through families and is characterized by a single gene mutation, multiple gene mutations, or chromosomal abnormalities. Diagnosing genetic diseases usually relies on genetic testing, which analyzes DNA to detect genetic changes that may cause the disease. However, the diagnostic process is complex. This is because some hereditary diseases may have delayed-onset symptoms or exhibit significant phenotypic variation. In addition, the interaction of environmental and genetic factors may affect the diagnosis of the disease.

Market Analysis of Genetic Disease Diagnostics

In Vitro Diagnostic of Genetic Disease

In vitro diagnostics (IVDs) are medical tests or diagnostic procedures performed in a controlled laboratory environment using samples such as blood, urine, and other bodily fluids. These tests can help accurately identify genetic abnormalities and genetic diseases, which is crucial for early diagnosis and personalized treatment. Below are some IVD test kits designed for common genetic diseases.

Our Solutions

As a global leading supplier of IVD products, Alta DiagnoTech has delved deeply into the field of precise genetic disease detection and launched a series of genetic disease detection kits covering the entire life cycle. This product line utilizes human samples such as blood, urine, saliva, and tissue, combined with cutting-edge technologies such as high-throughput sequencing (NGS) and quantitative PCR, to enable precise screening, diagnosis, and dynamic monitoring of conditions such as single-gene disorders, chromosomal abnormalities, mitochondrial diseases, and genetic tumor susceptibility.

IVD Solutions for Genetic Disease

Genetic Screening Kits

Molecular Diagnostics Products

NGS Solutions

Genetic Screening Kits

Our genetic screening kit is easy to use and provides rapid initial screening for large populations, accurately identifying potential genetic disease risk signals. It provides strong support for the early detection and timely intervention of genetic problems, helping to improve overall health. Specific coverage:

• Newborn Genetic Disease Screening Kits
• Pre-pregnancy/Prenatal Genetic Screening Kits
• Carrier Screening Kits

• Cancer Genetic Risk Screening Kits
• Cancer Genetic Risk Screening Kits
• Drug Metabolism Gene Screening Kits

Molecular Diagnostics Products

Relying on advanced molecular detection technology, our molecular diagnostic products cover the genetic level and accurately identify gene mutations related to various genetic diseases, providing a solid and reliable basis for accurate diagnosis, detailed classification, and the formulation of personalized treatment plans. Specific coverage:

• qPCR/RT-PCR Reagents
• Virus Integration Detection Kits
• Pathogenic Mutation Detection Panels

• Gene Chips
• Microarray Kits
• Single Gene Detection Kits

NGS Solutions

Our next-generation sequencing technology (NGS) solutions utilize high-throughput sequencing technology to comprehensively and deeply analyze genomic information, efficiently identifying rare and unknown genetic variations, and providing powerful and effective tools for the precise diagnosis and in-depth research of complex genetic diseases. Specific coverage:

• Whole Exome Sequencing (WES) Kits
• Whole Genome Sequencing (WGS) Kits
• Plasmid Library Construction Products

• Targeted Sequencing Panels
• Multi-omics Sequencing Instruments
• Sequencing Chips

Types of Genetic Diseases

Applications

Advantages

• Precision Detection Technology: Based on NGS and advanced algorithms, the products enable precise identification of pathogenic mutations at the single-base level, providing reliable evidence for clinical diagnosis.
• Comprehensive Disease Coverage: The product covers a wide range of genetic disease types, including rare and common genetic disorders, supporting early diagnosis and treatment of genetic diseases.
• Multi-Omics Integration: Simultaneous detection of genomic DNA, mitochondrial DNA, and epigenetic markers significantly improves diagnostic accuracy for complex diseases.
• Rapid Turnaround Time: Our solution combines automated processes with sequencing technology to enable rapid sample testing.

Alta DiagnoTech integrates cutting-edge technologies and continuous innovation to lead the field of genetic disease diagnostics. We offer a comprehensive range of IVD products, enabling early detection, personalized treatment, and improved patient outcomes. From single-gene mutation analysis to multi-gene panel testing, our IVD solutions are precisely tailored to the specific application scenarios in the genetic disease field. If you need more information about our products or want a quote, please feel free to contact us!