• Oncology
  • Multiple Myeloma
  • Cystic Fibrosis
  • Spinal Muscular Atrophy
  • Fragile X Syndrome
  • Beta Thalassemia
  • Sickle Cell Disease/Trait
  • Duchane Muscular Dystrophy
  • Congenital Adrenal Hyperplasia
  • Alpha Thalassemia
  • Intellectual disability
  • Congenital glaucoma
  • Bardet–Biedl syndrome
  • Meckel– Gruber syndrome
  • organic acidaemia
  • lysosomal storage disorders
  • retinal dystrophies
  • Hearing loss and primary microcephaly
  • Thrombocytopenia
  • Spherocytosis
  • Hemolytic anemia
  • G6PD deficient
  • C6 deficiency
  • Aminoacylase 1 deficiency
  • Sitosterolemia 2
  • Chronic granulomatous disease
  • Breast Cancer
  • Ovarian Cancer
  • Acute Myeloid Leukemia
  • Hodgkin Lymphoma
  • Non-Hodgkin Lymphoma

Minagene's WAGR Syndrome (PAX6 and WT1) Gene Sequencing

Minagene's Congenital Adrenal Hyperplasia (CAH) Genetic Testing

Minagene's Clinical Exome V4

Minagene's Trio Exome Test


Whole Exome Sequencing

Minagene's Oncopharmacogenomics of Thiopurines

Minagene's Oncopharmacogenomics of Fluoropyrimidines

Minagene's Tumor Mutation Burden (TMB) Test

Minagene's FLT3 Test

Minagene's Hemophagocytic Lymphohistiocytosis (HLH) Gene Panel

Minagene's Non-Small Cell Lung Cancer (NSCLC) Panel

Minagene's Comprehensive Leukemia Panel

Minagene's EGFR Gene Testing

Minagene's NGS-based Imatinib Resistance Mutation Analysis

Minagene's OncoTrack

Minagene's Somatic Mutation Panel

Minagene’s Molecular Testing for Lung Cancer

Minagene’s Germline Mutation Test for Hereditary Cancers

Minagene’s Molecular Testing for Hematological Malignancies

Minagene’s Comprehensive Tumor Gene Panel

Minagene’s Homologous Recombination Repair Gene Testing

Minagene’s BRCA

Minagene’s Carrier Screening

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