WHOLE EXOME SEQUENCING
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WHOLE EXOME SEQUENCING
NGS ONCOMINE FOCUS ASSAY (52 GENES, DNA MUTATIONS, CNVS, RNA FUSIONS)
AUTOIMMUNE ENCEPHALITIS PANEL , CSF
NGS BRCA1 & 2(SOMATIC)ASSAY
NGS FOR HEREDITARY HEMOLYTIC ANEMIA (MEMBRANOPATHY AND ENZYMOPATHY)
NGS ONCOMINE MYELOID V2GX ASSAY
NGS BONE MARROW FAILURE SYNDROME GENE PANEL
UNIPHARMGX19
NGS B CELL CLONALITY
UNICAD NIPT ADVANCE
NGS B CELL CLONALITY
AUTOIMMUNE ENCEPHALITIS PANEL , SERUM
NGS FOR HEREDITARY HEMOLYTIC ANEMIA (MEMBRANOPATHY AND ENZYMOPATHY)
NGS ONCOMINE MYELOID V2GX ASSAY
NGS OMIXOME SOLO (CES+MTDNA+CNV)
NGS TYPICAL AND ATYPICAL HUS
NGS CARDIOMYOPATHY
PCR THALASSEMIA COMPLETE WORK-UP
FETAL RHD GENOTYPING (NON-INVASIVE RHESUS-D DETECTION)
NGS HYPERTROPHIC CARDIOMYOPATHY
NGS NEPHROTIC SYNDROME GENE PANEL
NGS HEMOPHILIA A AND B(FACTOR VIII AND FACTOR IX)
KNOWN MUTATION CONFIRMATION BY SANGER SEQUENCING- 3 VARIANT
MICROARRAY 750K
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