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• Molecular characterization of Acute Leukemia panels by RT-PCR:
• Molecular characterization of ALL by RT-PCR: Fusion genes t(12;21), t(1;19), t(4;11), t(9;22) p190 and t(9;22)p210
• Molecular characterization of AML by RT-PCR: Fusion genes for AML as t(8;21), inversion 16 and of M3
• Molecular detection of Philadelphia chromosome by RT-PCR: t(9;22) P210and P190
• Single fusion gene for acute leukemia can be done separately: t(12;21), t(1;19), t(4;11), t(9;22)P190 and P210, t(8;21), inversion 16 and t(15;17)
• MRD by molecular for ALL
• MRD by molecular for AML
• MRD by Molecular for CML by GeneXpert Instrument Systems
• MRD by WT1 gene expression in AML
• WT1 gene expression in AML
• Nucleophosmin Gene Mutation
• JAK2 (Janus Tyrosine Kinase) V617F Gene Mutation (exon 14)
• BCR-ABL Gene Mutation (Panel-7 Test)
• BCR-ABL Gene Mutation (one Test)

• HLA typing by luminex.
• Anti HLA antibody tests (PRA and Single Antigen Tests).
• Monitoring engraftment by short tandem repeats (STRs).
• Monitoring engraftment by variable number tandem repeats (VNTRs).
• Genetic profiling of JMML.
• FLT3 Internal Tandem Duplication (ITD).
• TPMT Genotyping.
• Factor V Leiden.

Working Hours:

• Every day from 8 am till 8 pm except Friday.

For reservations and inquires, call us on 19057

These services are provided for patients above 18 years old.

• Bone Marrow smear & procedure
• Bone Marrow Smear Interpretation
• Immuno-phenotyping Acute Leukemia
• Immuno-phenotyping Lymphoma
• MRD BY Flow Cytometry B phenotype ALL
• MRD BY Flow Cytometry T phenotype ALL
• MRD BY Flow Cytometry myeloid phenotype ANLL
• Chromosome analysis
• FISH (single probe)
• Molecular characterization of B-precursor ALL (Panel -4 Translocations)
• Molecular characterization of AML (t8;21),inv 16
• Molecular characterization of APL (M3)
• Molecular characterization of Mixed phenotype Acute Leukemia
• Nucleophosmin Gene Mutation
• WT1 gene expression in AML
• JAK2 (Janus Tyrosine Kinase)-2 Gene Mutation
• MRD By Molecular For CML (IS) (By Xpert BCR-ABL Ultra (Gene expert)
• MRD By Molecular For AML
• MRD By Molecular For Philadelphia positive ALL
• MRD by WT1 gene expression in AML
• Single translocation by RT-PCR
• BCR-ABL Gene Mutation (Panel- 7 tests)
• BCR-ABL Gene Mutation (1 Test)
• FLT3 internal Tandem duplication(ITD)
• Molecular profiling of JMML

Working Hours:

• Every day from 8 am till 8 pm except Friday.

For reservations and inquires, call us on 19057

These services are provided for patients above 18 years old.

NGS is an advanced technology that refers to high throughput genome assays at high accuracy and reasonable price. It does not only produce massive amount of genetic information, but it also establishes a foundation for personalized genomic medicine as a part of standard medical care.

Sequencing machines:

It is a tool that helps in providing precise medical diagnosis of genetic diseases and in transforming genetic information into actionable results for physicians and patients.

• MiSeq DX is an FDA regulated and CE-IVD marked sequencer for invitro diagnostic testing.

It can be used for Targeted Gene Panel: A select set of genes or gene regions that have proven or suspected associations with the disease or phenotype under study.

• NextSeq 550 System provides a high-resolution, base-by-base view of the genome, which is highly informative in testing for whole-genome, whole exome, transcriptome, and targeted resequencing.

NGS Gene panels:

• Familial cancer:
• Genetic testing for hereditary cancer.
• Familial breast cancer, Hereditary breast and ovarian cancer, Familial male breast cancer.
• Hereditary thyroid cancer.
• Hereditary non-polyposis colorectal cancer.
• Lynch syndrome.
• Hereditary brain tumors.
• Mismatch repair cancer syndrome.
• Neurofibromatosis Type 1 & 2.
• Li-Fraumeni Syndrome.


• Bone marrow Failure:

Caused by many genetic mutations resulting in reduced or abnormal production of one or more of the three blood cell types (red blood cell, white blood cell and platelets). Example: Fanconi anemia, Dyskeratosis congenita, Diamond Blackfan anemia and Shwachman Diamond syndrome. There may be increased risk of cancer development.



• Neurological disorders:
• Hereditary cerebellar ataxias.
• Muscular Dystrophy (Duchenne muscular , Becker muscular dystrophy, etc..).
• Dystonia.
• Dementia.


• Cardiac Disorders:
• Hypertrophic cardiomyopathy.
• Dilated cardiomyopathy.


• Ophthalmic conditions:
• Optic Atrophy.
• Familial retinoblasotma.


• Metabolic Disorders:
• Lysosomal storage
• Familial hypercholesterolemia


• Inherited kidney diseases:
• Tuberous sclerosis.
• Von Hippel Lindau syndrome.
• Congenital renal parynchemal disease.
• Congenital polycyctic kidney.


• Hereditary hearing loss:

Hereditary non-syndromic (isolated) deafness.

• Genomic Profiling of ALL:

Targeted RNA sequencing of genes including those relevant to acute lymphoblastic leukemia particularly Philadelphia-like ALL.



• Hematological neoplasms (molecular biology unit):

Molecular Genetic Profiling of AML (wide panel) Molecular Genetic Profiling of Myeloid Neoplasm (MDS-Myeloid neoplasm) (wide panel).

Working Hours:

• Every day from 8 am till 8 pm except Friday.

For reservations and inquires, call us on 19057

These services are provided for patients above 18 years old.