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

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Achondroplasia
Assesses the hereditary risk of achondroplasia, a common cause for dwarfism
Achondroplasia
Reporting reproductive risk for couples with 400+ most common diseases
Ankylosing spondylitis
Assesses the hereditary risk of ankylosing spondylitis, a degenerative arthritis that affects the spine and joints
Azoospermia
Assesses the hereditary risk of Azoospermia, a condition that affects the sperm count in a man's ejaculate
Blood cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Blood cancer
Reporting reproductive risk for couples with 400+ most common diseases
Blood cancer
Detects pathogenic mutations in 43 genes which are related to Acute myelogenous leukemia
Blood cancer
Detects pathogenic mutations in 76 most common genes which are related to 5 different types of blood cancer
Breast cancer
Detects all the pathogenic mutations in BRCA1 and BRCA2 that commonly increases the risk for hereditary breast and ovarian cancer
Breast cancer
Detects large mutations in BRCA1 and BRCA2 that increases the risk for hereditary breast and ovarian cancer
Breast cancer
Scans 29 regions in BRCA1 and BRCA2 that increases the risk for hereditary breast and ovarian cancer in Asian population
Breast cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Breast cancer
Assesses120 most common hereditary cancer diseases.
Breast cancer
Detects pathogenic mutations in 37 genes which are commonly observed in solid tumor
Breast cancer
Screens for 170 cancer mutation fusions that leads to cancer activaties in solid tumor
Calpainopathy
Detects CAPN3 gene mutation which causes calpainopathy
Cervical cancer
Identifies 33 known HPV types which may lead to cervical cancer and genital warts. (Companion testing with Pap test optional)
Colorectal cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Colorectal cancer
Assesses120 most common hereditary cancer diseases.
Colorectal cancer
Detects pathogenic mutations in 3 most common genes which are related to colorectal cancer
Colorectal cancer
Detects BRAF gene mutations which relates to various types of cancers
Colorectal cancer
Detects pathogenic mutations in KRAS and NRAS, which are related to colorectal cancer
Colorectal cancer
Detects KRAS mutations in solid tumor cancer genes
Colorectal cancer
Detects pathogenic mutations in 37 genes which are commonly observed in solid tumor
Colorectal cancer
Screens for 170 cancer mutation fusions that leads to cancer activaties in solid tumor
Cystic fibrosis
Assesses the hereditary risk of cystic fibrosis, a disease that can damage the respiratory and digestive system
Cystic fibrosis
Reporting reproductive risk for couples with 400+ most common diseases
Down’s syndrome
Reporting reproductive risk for couples with 400+ most common diseases
Down’s syndrome
Screens for genetic disorders (Trisomy) in newborns that lead to mental retardation and developmental issues
Duchenne and Becker muscular dystrophy
Assesses DMD gene condition which relates to Duchenne and Becker muscular dystrophy
Duchenne and Becker muscular dystrophy
Reporting reproductive risk for couples with 400+ most common diseases
Edward syndrome
Reporting reproductive risk for couples with 400+ most common diseases
Edward syndrome
Screens for genetic disorders (Trisomy) in newborns that lead to mental retardation and developmental issues
Endocrine cancer
Assesses120 most common hereditary cancer diseases.
Endocrine cancer
Detects BRAF gene mutations which relates to various types of cancers
Eye infection in new-born baby
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Fragile X syndrome
Assesses the hereditary risk of fragile X syndrome, a condition that leads to mental retardation
Fragile X syndrome
Reporting reproductive risk for couples with 400+ most common diseases
Head & Neck cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Head & Neck cancer
Assesses120 most common hereditary cancer diseases.
Heart conditions
Assesses the hereditary risk of 8 most common Cardiomyopathies and Sudden Arrythmic Death Syndrome which can cause sudden cardiac death
Infertility
Assesses the hereditary risk of Azoospermia, a condition that affects the sperm count in a man's ejaculate
Infertility
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Kidney cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Kidney cancer
Assesses120 most common hereditary cancer diseases.
Lung cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Lung cancer
Detects pathogenic mutations in 23 most common genes which are related to non-small cell lung cancer
Lung cancer
Detects ALK gene fusions which leads to non-small cell lung cancer
Lung cancer
Detects KRAS mutations in solid tumor cancer genes
Lung cancer
Detects EML4-ALK gene fusions which leads to non-small cell lung cancer
Lung cancer
Detects ROS1 gene fusions which leads to non-small cell lung cancer
Lung cancer
Detects EGFR mutations in solid tumor cancer genes
Lung cancer
Detects pathogenic mutations in 37 genes which are commonly observed in solid tumor
Lung cancer
Screens for 170 cancer mutation fusions that leads to cancer activaties in solid tumor
Lung cancer
Detects EGFR mutations in circulating cell free tumor DNA (cfDNA)
Neuroblastoma
The premium service which screens for 2700+ genes, 900+diseases in one single test
Neuroblastoma
Assesses120 most common hereditary cancer diseases.
Neurofibromatosis
The premium service which screens for 2700+ genes, 900+diseases in one single test
Neurofibromatosis
Assesses120 most common hereditary cancer diseases.
Ovarian cancer
Detects all the pathogenic mutations in BRCA1 and BRCA2 that commonly increases the risk for hereditary breast and ovarian cancer
Ovarian cancer
Detects large mutations in BRCA1 and BRCA2 that increases the risk for hereditary breast and ovarian cancer
Ovarian cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Ovarian cancer
Assesses120 most common hereditary cancer diseases.
Ovarian cancer
Detects BRAF gene mutations which relates to various types of cancers
Ovarian cancer
Detects pathogenic mutations in 37 genes which are commonly observed in solid tumor
Ovarian cancer
Screens for 170 cancer mutation fusions that leads to cancer activaties in solid tumor
Pancreatic cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Pancreatic cancer
Assesses120 most common hereditary cancer diseases.
Paraganglimo cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Paraganglimo cancer
Assesses120 most common hereditary cancer diseases.
Patau syndrome
Screens for genetic disorders (Trisomy) in newborns that lead to mental retardation and developmental issues
Pelvic Inflammatory Disease
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Premature labour
Assesses the hereditary risk of thrombophilia, a condition associated with an increased risk of pregnancy loss
Premature labour
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Prenatal genetic conditions
Reporting reproductive risk for couples with 400+ most common diseases
Prenatal inherited diseases
Reporting reproductive risk for couples with 400+ most common diseases
Prostate cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Prostate cancer
Assesses120 most common hereditary cancer diseases.
Prostate cancer
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Rare inherited diseases
The premium service which screens for 2700+ genes, 900+diseases in one single test
Rare inherited diseases
Reporting reproductive risk for couples with 400+ most common diseases
Retinoblastoma
The premium service which screens for 2700+ genes, 900+diseases in one single test
Retinoblastoma
Assesses120 most common hereditary cancer diseases.
Sexually transmitted disease (STD)
Identifies 33 known HPV types which may lead to cervical cancer and genital warts. (Companion testing with Pap test optional)
Sexually transmitted disease (STD)
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Skin cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Skin cancer
Assesses120 most common hereditary cancer diseases.
Skin cancer
Detects BRAF gene mutations which relates to various types of cancers
Spinal muscular atrophy
Assesses the hereditary risk of spinal muscular atrophy, a neuromuscular disorder that leads to muscle weakness
Still-births
Assesses the hereditary risk of thrombophilia, a condition associated with an increased risk of pregnancy loss
Still-births
This test detects a wide range of STI pathogens using PCR and “Flow through” hybridization.
Stomach cancer
The premium service which screens for 2700+ genes, 900+diseases in one single test
Stomach cancer
Assesses120 most common hereditary cancer diseases.
Stomach cancer
Detects pathogenic mutations in 23 most common genes which are found in gastro-intestinal stromal tumors
Stomach cancer
Detects pathogenic mutations in 37 genes which are commonly observed in solid tumor
Stomach cancer
Screens for 170 cancer mutation fusions that leads to cancer activaties in solid tumor
Thrombophilia
Assesses the hereditary risk of thrombophilia, a condition associated with an increased risk of pregnancy loss
Trisomy X, Y syndrome
Reporting reproductive risk for couples with 400+ most common diseases
Trisomy X, Y syndrome
Screens for genetic disorders (Trisomy) in newborns that lead to mental retardation and developmental issues
α thalassemia
Assesses the hereditary risk of α-thalassemia
α thalassemia
Reporting reproductive risk for couples with 400+ most common diseases
β thalassemia
Assesses the hereditary risk of β-thalassemia
β thalassemia
Reporting reproductive risk for couples with 400+ most common diseases