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    BRCA1 & BRCA2 Panel
    Lung Cancer Liquid Biopsy Panel
    Oncomine Myeloid Panel
    PAN Cancer Liquid Biopsy Panel
    TP53 & IGHV Panel
    Solid Tumors
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    Non-Invasive Prenatal Screening (NIPT)
    NIPS- Microdeletions
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    Pre-Implantation Genetic testing- Aneuploidy
    Pre-Implantation Genetic testing- Mutations
    Fragile X carrier Scrrening
    Sperm DNA fragmentation analysis
    Y chromosome microdeletions
    Infertility panels
    Cytogenetics
    Couple Karyotype
  • Rare Diseases
    Comprehensive assays
    ExomePlus
    Whole Genome Sequencing
    Whole Exome Sequencing
    Clinical Exome Sequencing
    Trio Whole exome Seqeuncing
    Affymetrix Cytoscan 750k array
    Affymerix Cytoscan 315k array
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    Targeted assays
    Beta Thalassemia
    Alpha Thalassemia
    SMA by MLPA
    DMD by MLPA
    Spinocerebellar ataxia (SCA) Panel
    Fragile X Syndrome
    Congenital adrenal hyperplasia (CAH))
    Huntington disease
    Gilbert Syndrome
    Cystic Fibrosis
    Achondroplasia
    QF PCR
    Crigler Najjar Syndrome
    RETT syndrome
    HLA B27 Study
    Custom Targeted mutation analysis
  • Contact Us
support@rophevacbiolabz.com
+918310968374
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Rophevac Bio Labz Rophevac Bio Labz
  • Home
  • Oncology
    Panels
    GenomeSignature Panel
    Comprehensive Genomic Profile
    Sarcoma Expanded panel
    Oncomine Focus panel
    HRD Mutations Panel
    Oncomine Comprehensive Panel
    Tumor Mutation Burden
    Target25 Solid panel
    BRCA1 & BRCA2 Panel
    Lung Cancer Liquid Biopsy Panel
    Oncomine Myeloid Panel
    PAN Cancer Liquid Biopsy Panel
    TP53 & IGHV Panel
    Solid Tumors
    Lung Cancer
    Breast & Ovarian Cancer
    Colon cancer
    Glioma
    Sarcoma
    Prostate cancer
    Cholangiocarcinoma
    Thyroid Cancer
    Hematological Malignancies
    Acute Myeloid Leukemia (AML)
    Chronic Myeloid Leukemia (CML)
    Acute Lymphocytic Leukemia (ALL)
    Chronic Lymphocytic Leukemia (CLL)
    Lymphoma
  • Reproductive health
    Genomics
    Non-Invasive Prenatal Screening (NIPT)
    NIPS- Microdeletions
    Couple Carrier Screening
    Pre-Implantation Genetic testing- Aneuploidy
    Pre-Implantation Genetic testing- Mutations
    Fragile X carrier Scrrening
    Sperm DNA fragmentation analysis
    Y chromosome microdeletions
    Infertility panels
    Cytogenetics
    Couple Karyotype
  • Rare Diseases
    Comprehensive assays
    ExomePlus
    Whole Genome Sequencing
    Whole Exome Sequencing
    Clinical Exome Sequencing
    Trio Whole exome Seqeuncing
    Affymetrix Cytoscan 750k array
    Affymerix Cytoscan 315k array
    Panels
    Neurology
    Metabolic Disorders
    Hereditary Cancer
    Malformations
    Immunology
    Hematology
    Mitochondrial Disorders
    Nephrology
    Cardiology
    Dermatology
    Endocrinology
    Ophthalmology
    Targeted assays
    Beta Thalassemia
    Alpha Thalassemia
    SMA by MLPA
    DMD by MLPA
    Spinocerebellar ataxia (SCA) Panel
    Fragile X Syndrome
    Congenital adrenal hyperplasia (CAH))
    Huntington disease
    Gilbert Syndrome
    Cystic Fibrosis
    Achondroplasia
    QF PCR
    Crigler Najjar Syndrome
    RETT syndrome
    HLA B27 Study
    Custom Targeted mutation analysis
  • Contact Us

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