Multimodal Panels
These are genetic tests designed to analyze different types of biological data simultaneously. These panels typically combine DNA, RNA, and epigenetic information (such as methylation data) to create a more comprehensive biological profile. This approach allows for a better understanding of complex diseases, such as cancer, and facilitates the development of personalized treatment strategies.
WGS (Whole Genome Sequencing)
It is a technique for determining the entire DNA sequence of an organism. This method examines the entire genetic material to create a detailed map of genes, regulatory regions, and other genetic elements. WGS is widely used in fields such as genetic disease research, cancer genetics, evolutionary biology, and biomedical research.
WES (Whole Exome Sequencing)
It is a genetic analysis method that sequences the entire exome of an organism. The exome refers to the protein-coding regions of genes, which make up only about 1-2% of the entire genome. Therefore, WES is a highly effective method in the study of genetic diseases, particularly in identifying hereditary conditions.
CES (Clinical Exome Sequencing)
Clinical exome sequencing is a molecular genetic test used in the diagnosis of genetic diseases in individuals. The “exome” refers to the protein-coding regions of the genome, which make up about 1% of the human genome. This test aims to detect genetic mutations by sequencing only the exomes from the patient’s genetic material. Clinical exome […]
Targeted DNA/RNA Panels
NGS panels focused on the analysis of specific genes or gene groups. These panels are commonly used for diagnosing hereditary diseases, cancer genetics, and investigating other genetic disorders. Targeted panels are designed to detect specific genetic variations, offering a faster and more cost-effective solution compared to whole genome sequencing methods.
Genetic diseases
Genetic diseases are health issues that arise as a result of changes or mutations in genes. These diseases can be hereditary (passed down from family) or acquired (developed during life). Genetic diseases typically cause disruptions in the function of a specific gene or group of genes, which in turn affects the normal functioning of cells.
Hemato-oncology
Hematologic cancers encompass cancer types and other blood disorders that affect the blood system. These diseases arise due to abnormal growth or dysfunction of blood cells.
Somatic cancers
Somatic cancers are types of cancer that arise as a result of genetic changes occurring in the cells of the body. These cancers typically develop due to environmental factors, lifestyle choices, or the aging process that an individual is exposed to throughout their life. Somatic cancers vary from person to person, and treatment approaches are […]
Hemato-oncology
Hematologic cancers include cancer types and other blood disorders that affect the blood system. These diseases arise due to abnormal growth of blood cells or disruptions in their functionality.
Genetic diseases
Genetic diseases are health issues that arise as a result of changes or mutations in genes. These diseases can be hereditary (passed down from family) or acquired (developed during life). Genetic diseases typically cause disruptions in the function of a specific gene or group of genes, which affects the normal functioning of cells.
Designable (Custom) DNA/RNA Panels
These are NGS panels designed according to specific research needs or clinical conditions. These panels allow users to target specific genes or gene groups of interest, enabling more customized and meaningful results.
Methylation Detection Panels
These are specialized genetic analysis tools designed to study DNA methylation. DNA methylation is a significant epigenetic modification that regulates gene expression. Methylation levels can affect cell function and the development of genetic diseases. These panels aim to uncover genetic and epigenetic information by targeting specific methylation regions.
