Find the test best matched to your needs

We aim to always provide access to the most useful and latest diagnostic tools. The following list is alphabetical by condition, and can be filtered by test category, and searched by condition.

Hereditary risk assessments
Precision cancer tests
Prenatal and women’s health tests
Condition
Test
 
Description

No Results Found

Achondroplasia
Achondroplasia mutation
Assesses the hereditary risk of achondroplasia, a common cause for dwarfism
Ankylosing spondylitis
HLA B27 Screening
Assesses the hereditary risk of ankylosing spondylitis, a degenerative arthritis that affects the spine and joints
Azoospermia
Y-chromosome microdeletion
Assesses the hereditary risk of Azoospermia, a condition that affects the sperm count in a man's ejaculate
Blood cancer
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Blood cancer
Cquence AML/MDS genotyping panel
Detects pathogenic mutations in 43 genes which are related to Acute myelogenous leukemia
Blood cancer
Cquence pan-heme panel
Detects pathogenic mutations in 76 most common genes which are related to 5 different types of blood cancer
Breast cancer
Mygenia BRCA1 and BRCA2 panel
Detects all the pathogenic mutations in BRCA1 and BRCA2 that commonly increases the risk for hereditary breast and ovarian cancer
Breast cancer
BRCA1 & 2 MLPA screening
Detects large mutations in BRCA1 and BRCA2 that increases the risk for hereditary breast and ovarian cancer
Breast cancer
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Breast cancer
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Breast cancer
PanBRCA™ Inherited Breast & Ovarian Cancer Screening Test
Screening all exons on BRCA1 & 2 for gene mutations covering up to 99.9% of Asian common mutations for ladies
Breast cancer
Cquence solid tumor panel
Detects pathogenic mutations in 37 genes which are commonly observed in solid tumor
Breast cancer
Cquence solid tumor fusion gene panel
Screens for 170 cancer mutation fusions that leads to cancer activaties in solid tumor
Calpainopathy
CAPN3 gene analysis
Detects CAPN3 gene mutation which causes calpainopathy
Cervical cancer
Mygenia ctDNA - Early Cancer Screening
Provide early detection of cancer and allow you to take action in time
Cervical cancer
HPV9 Antibody Test (Advance)
Designed for people who are vaccinated against HPV
Cervical cancer
HPV DNA genotyping
Identifies 33 known HPV types which may lead to cervical cancer and genital warts. (Companion testing with Pap test optional)
Cervical cancer
Cervical Cancer HPV DNA test
HPV DNA test features a self-collection kit; simple and easy protection for your health,
Colorectal cancer
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Colorectal cancer
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Colorectal cancer
Cquence colorectal cancer mutation panel
Detects pathogenic mutations in 3 most common genes which are related to colorectal cancer
Colorectal cancer
BRAF mutation screening
Detects BRAF gene mutations which relates to various types of cancers
Colorectal cancer
Colorectal cancer genes package (KRAS & NRAS)
Detects pathogenic mutations in KRAS and NRAS, which are related to colorectal cancer
Colorectal cancer
KRAS mutation screening
Detects KRAS mutations in solid tumor cancer genes
Colorectal cancer
Cquence solid tumor panel
Detects pathogenic mutations in 37 genes which are commonly observed in solid tumor
Colorectal cancer
Cquence solid tumor fusion gene panel
Screens for 170 cancer mutation fusions that leads to cancer activaties in solid tumor
Colorectal cancer
Mygenia ctDNA - Early Cancer Screening
Provide early detection of cancer and allow you to take action in time
Cystic fibrosis
Cystic fibrosis mutation screening
Assesses the hereditary risk of cystic fibrosis, a disease that can damage the respiratory and digestive system
Down’s syndrome
Trisomy 21, 18, 13 & X, Y screening test
Screens for genetic disorders (Trisomy) in newborns that lead to mental retardation and developmental issues
Duchenne and Becker muscular dystrophy
DMD deletion / conversion analysis
Assesses DMD gene condition which relates to Duchenne and Becker muscular dystrophy
Duchenne and Becker muscular dystrophy
NJ Series Carrier Risk Assessment
Hereditary diseases carrier status in one test A comprehensive protection for you and your family
Edward syndrome
Trisomy 21, 18, 13 & X, Y screening test
Screens for genetic disorders (Trisomy) in newborns that lead to mental retardation and developmental issues
Endocrine cancer
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Endocrine cancer
BRAF mutation screening
Detects BRAF gene mutations which relates to various types of cancers
Endocrine cancer
Mygenia ctDNA - Early Cancer Screening
Provide early detection of cancer and allow you to take action in time
Eye infection in new-born baby
STD DNA screening
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Fragile X syndrome
Fragile X screening
Assesses the hereditary risk of fragile X syndrome, a condition that leads to mental retardation
Fragile X syndrome
NJ Series Carrier Risk Assessment
Hereditary diseases carrier status in one test A comprehensive protection for you and your family
Head & Neck cancer
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Head & Neck cancer
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Head & Neck cancer
Mygenia ctDNA - Early Cancer Screening
Provide early detection of cancer and allow you to take action in time
Heart conditions
Mygenia Cardiac Health Risk Assessment
Assesses the hereditary risk of 23 cardiac diseases, including 6 Sudden Arrhythmia Death Syndromes and various myocardium related diseases
Infertility
Y-chromosome microdeletion
Assesses the hereditary risk of Azoospermia, a condition that affects the sperm count in a man's ejaculate
Infertility
STD DNA screening
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Kidney cancer
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Kidney cancer
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Lung cancer
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Lung cancer
Cquence NSCLC genotyping panel
Detects pathogenic mutations in 23 most common genes which are related to non-small cell lung cancer
Lung cancer
KRAS mutation screening
Detects KRAS mutations in solid tumor cancer genes
Lung cancer
ROS1 gene fusion screening
Detects ROS1 gene fusions which leads to non-small cell lung cancer
Lung cancer
Cquence solid tumor panel
Detects pathogenic mutations in 37 genes which are commonly observed in solid tumor
Lung cancer
Cquence solid tumor fusion gene panel
Screens for 170 cancer mutation fusions that leads to cancer activaties in solid tumor
Lung cancer
ALK FISH Test
Detects ALK gene fusions which leads to non-small cell lung cancer
Lung cancer
EGFR mutation plasma screening
Detects EGFR mutations in circulating cell free tumor DNA (cfDNA)
Lung cancer
EML4-ALK fusion gene screening
Detects EML4-ALK gene fusions which leads to non-small cell lung cancer
Lung cancer
EGFR mutation screening
Detects EGFR mutations in solid tumor cancer genes
Lung cancer
Mygenia ctDNA - Early Cancer Screening
Provide early detection of cancer and allow you to take action in time
Lung cancer
Mygenia ctDNA - Early Cancer Screening
Provide early detection of cancer and allow you to take action in time
Neuroblastoma
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Neuroblastoma
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Neurofibromatosis
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Neurofibromatosis
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Ovarian cancer
Mygenia BRCA1 and BRCA2 panel
Detects all the pathogenic mutations in BRCA1 and BRCA2 that commonly increases the risk for hereditary breast and ovarian cancer
Ovarian cancer
BRCA1 & 2 MLPA screening
Detects large mutations in BRCA1 and BRCA2 that increases the risk for hereditary breast and ovarian cancer
Ovarian cancer
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Ovarian cancer
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Ovarian cancer
PanBRCA™ Inherited Breast & Ovarian Cancer Screening Test
Screening all exons on BRCA1 & 2 for gene mutations covering up to 99.9% of Asian common mutations for ladies
Ovarian cancer
BRAF mutation screening
Detects BRAF gene mutations which relates to various types of cancers
Ovarian cancer
Cquence solid tumor panel
Detects pathogenic mutations in 37 genes which are commonly observed in solid tumor
Ovarian cancer
Cquence solid tumor fusion gene panel
Screens for 170 cancer mutation fusions that leads to cancer activaties in solid tumor
Pancreatic cancer
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Pancreatic cancer
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Pancreatic cancer
Mygenia ctDNA - Early Cancer Screening
Provide early detection of cancer and allow you to take action in time
Paraganglimo cancer
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Paraganglimo cancer
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Patau syndrome
Trisomy 21, 18, 13 & X, Y screening test
Screens for genetic disorders (Trisomy) in newborns that lead to mental retardation and developmental issues
Pelvic Inflammatory Disease
STD DNA screening
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Premature labour
Thrombophilia test
Assesses the hereditary risk of thrombophilia, a condition associated with an increased risk of pregnancy loss
Premature labour
STD DNA screening
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Prostate cancer
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Prostate cancer
Prostate Cancer Screeing Test (BRCA1+2 & PSA)
Professional protection of your health
Prostate cancer
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Prostate cancer
Mygenia ctDNA - Early Cancer Screening
Provide early detection of cancer and allow you to take action in time
Prostate cancer
STD DNA screening
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Rare inherited diseases
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Retinoblastoma
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Retinoblastoma
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Sexually transmitted disease (STD)
HPV DNA genotyping
Identifies 33 known HPV types which may lead to cervical cancer and genital warts. (Companion testing with Pap test optional)
Sexually transmitted disease (STD)
STD DNA screening
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Skin cancer
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Skin cancer
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Skin cancer
BRAF mutation screening
Detects BRAF gene mutations which relates to various types of cancers
Spinal muscular atrophy
SMA SMN1&2 Deletion/ Conversion Analysis
Assesses the hereditary risk of spinal muscular atrophy, a neuromuscular disorder that leads to muscle weakness
Spinal muscular atrophy
NJ Series Carrier Risk Assessment
Hereditary diseases carrier status in one test A comprehensive protection for you and your family
Still-births
Thrombophilia test
Assesses the hereditary risk of thrombophilia, a condition associated with an increased risk of pregnancy loss
Still-births
STD DNA screening
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Stomach cancer
Mygenia One Health Risk Assessment
The premium service which screens for 2700+ genes, 900+diseases in one single test
Stomach cancer
Mygenia Cancer Health Risk Assessment Test
Assesses120 most common hereditary cancer diseases.
Stomach cancer
Cquence GIST genotyping panel
Detects pathogenic mutations in 23 most common genes which are found in gastro-intestinal stromal tumors
Stomach cancer
Cquence solid tumor panel
Detects pathogenic mutations in 37 genes which are commonly observed in solid tumor
Stomach cancer
Cquence solid tumor fusion gene panel
Screens for 170 cancer mutation fusions that leads to cancer activaties in solid tumor
Thrombophilia
Thrombophilia test
Assesses the hereditary risk of thrombophilia, a condition associated with an increased risk of pregnancy loss
Trisomy X, Y syndrome
Trisomy 21, 18, 13 & X, Y screening test
Screens for genetic disorders (Trisomy) in newborns that lead to mental retardation and developmental issues
α thalassemia
Alpha(α)-thalassemia mutation screening
Assesses the hereditary risk of α-thalassemia
α thalassemia
NJ Series Carrier Risk Assessment
Hereditary diseases carrier status in one test A comprehensive protection for you and your family
β thalassemia
Beta(β)-thalassemia mutation screening
Assesses the hereditary risk of β-thalassemia
β thalassemia
NJ Series Carrier Risk Assessment
Hereditary diseases carrier status in one test A comprehensive protection for you and your family