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Welcome to Sanket Genomics

Redefining precision diagnostics with advanced genetic testing and reliable care

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Backed by 30+ years of diagnostic excellence, Sanket brings world-class genomics closer to you.

Trusted Experts & Next-Gen Technology

Where Expertise Meets Innovation in Genomics

At Sanket Genomics, every test is powered by decades of diagnostic experience and the latest genomic technologies. From hereditary conditions to prenatal abnormalities and cancers, our services are designed to provide early and accurate diagnoses, enabling timely interventions and personalized treatment plans.

Our laboratories combine global expertise, ensuring world-class quality standards. Accredited by NHIMA and trusted by leading hospitals, we empower healthcare providers with cutting-edge tools for precise patient care and advanced therapeutic recommendations.

By strengthening public health, making advanced genetic tests affordable and accessible, and contributing to research and training, Sanket Genomics plays a vital role in enhancing Zambia's healthcare system. With over 2000 diagnostic tests, a strong legacy of serving more than a million patients, and state-of-the-art genomic platforms, we remain committed to improving outcomes and building healthcare equity in the region.

Shaping the Future of Genetic Testing in Zambia

At Sanket Genomics Laboratory Ltd, we combine global expertise with local commitment to bring advanced genetic testing to the heart of Lusaka. Our state-of-the-art facility supports patients with early and accurate diagnoses for prenatal conditions, hereditary syndromes, cancers, and infectious diseases.

By working closely with specialists across gynaecology, fertility, oncology, paediatrics, neurology, and general medicine, we ensure that every test result contributes to better patient care and timely clinical decisions. Beyond diagnostics, our laboratory also supports Zambia's healthcare system through training initiatives, research collaborations, and by making high-quality genetic testing accessible and affordable for all.

Lab Address: 2242 Independence Avenue, Woodlands, Lusaka, Zambia

Lab Hours: Monday to Saturday: 07:00 AM – 09:00 PM | Sunday: Closed

Reliable & High-Quality Genomics for Every Need

Click on a category below to explore our comprehensive range of advanced genetic tests.

Prenatal Genomics Testing

Genetic Testing for Syndromes

Cancer Genomics

Infectious Genetics Testing

Advanced Genomic & Metabolic Testing

1. Prenatal Genomics Testing

Early and accurate insights during pregnancy can help parents and doctors make informed decisions with confidence.

Non-Invasive Prenatal Testing (NIPT)

Special Instructions: Available from 10 weeks of pregnancy; blood sample required; no fasting needed.

Parameters Covered: Common trisomies (13, 18, 21), sex chromosomes, selected microdeletions.

Report Frequency: 7-10 days

Parameters: Screens for chromosomal abnormalities such as Down syndrome, Edwards syndrome, and Patau syndrome with high accuracy.

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Prenatal Karyotyping (Amniotic Fluid / CVS / POC)

Special Instructions: Sample from amniotic fluid, chorionic villus, or products of conception (POC).

Parameters Covered: 46 chromosomes.

Report Frequency: 2-3 weeks

Parameters: Detects extra/missing chromosomes and structural changes causing congenital disorders.

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Prenatal FISH Testing

Special Instructions: Sample depends on indication (amniotic fluid / CVS / POC).

Parameters Covered: Specific chromosomal regions.

Report Frequency: 5-7 days

Parameters: Rapid detection of common chromosomal abnormalities using fluorescent probes.

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POC Karyotyping and FISH

Special Instructions: Products of conception sample required.

Parameters Covered: 46 chromosomes + targeted chromosomal regions.

Report Frequency: 2–3 weeks (Karyotyping) / 5-7 days (FISH)

Parameters: Provides detailed genetic analysis of pregnancy loss cases to identify chromosomal causes.

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Chromosomal Microarray (Amniotic Fluid / CVS / POC)

Special Instructions: Amniotic fluid or CVS sample required; genetic counseling recommended.

Parameters Covered: Genome-wide copy number variations.

Report Frequency: 10-14 days

Parameters: High-resolution analysis for deletions, duplications, and microdeletions linked to genetic disorders.

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Pre-implantation Genetic Screening (PGS) / Diagnosis (PGD)

Special Instructions: Requires IVF embryos; performed before implantation.

Parameters Covered: Embryo chromosomes or specific gene mutations.

Report Frequency: 10-14 days

Parameters: Screens embryos for chromosomal aneuploidies or hereditary genetic conditions before transfer.

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Next Generation Sequencing (Infertility / Syndromes)

Special Instructions: Blood sample required; genetic counseling recommended.

Parameters Covered: ~20,000 protein-coding genes.

Report Frequency: 4-6 weeks

Parameters: Identifies genetic causes of infertility or congenital syndromes through exome sequencing.

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2. Genetic Testing for Syndromes

Understanding inherited and chromosomal syndromes early can guide treatment, support, and family planning decisions.

Couple Karyotype

Special Instructions: Blood samples required from both partners; no fasting needed.

Parameters Covered: 46 chromosomes for each partner.

Report Frequency: 7-10 days

Parameters: Detects extra/missing chromosomes and structural abnormalities that may cause infertility or recurrent pregnancy loss.

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Couple Microarray

Special Instructions: Blood samples required from both partners; genetic counseling recommended.

Parameters Covered: Genome-wide copy number variations.

Report Frequency: 10-14 days

Parameters: Detects subtle genetic changes, microdeletions, and duplications not visible in routine karyotyping.

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Y Chromosome Microdeletion

Special Instructions: Male blood sample required; no fasting needed.

Parameters Covered: Y chromosome microdeletion panel.

Report Frequency: 7-10 days

Parameters: Identifies genetic causes of male infertility due to deletions in the Y chromosome.

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Down, Edwards, Patau Syndrome

Special Instructions: Blood or prenatal sample depending on indication.

Parameters Covered: Trisomy 21, Trisomy 18, Trisomy 13.

Report Frequency: 7-10 days

Parameters: Detects common chromosomal trisomies responsible for developmental and congenital syndromes.

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Jacob, Klinefelter, Turner Syndrome

Special Instructions: Blood sample required.

Parameters Covered: Chromosomal analysis for sex chromosome aneuploidies.

Report Frequency: 7-14 days

Parameters: Identifies additional or missing sex chromosomes linked to growth, fertility, and developmental conditions.

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3. Cancer Genomics

Genetic insights play a vital role in cancer diagnosis, treatment planning, and monitoring to improve patient outcomes.

Cancer Karyotyping

Special Instructions: Bone marrow or blood sample required.

Parameters Covered: 46 chromosomes.

Report Frequency: 7-14 days

Parameters: Detects chromosomal abnormalities linked to leukemia, lymphoma, and other cancers.

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FISH for Blood Cancers (AML/ALL/CLL/etc.)

Special Instructions: Bone marrow or blood sample required.

Parameters Covered: Targeted chromosomal regions for hematological malignancies.

Report Frequency: 5-7 days

Parameters: Identifies specific genetic rearrangements and abnormalities critical for diagnosis and prognosis in blood cancers.

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Solid Tumor FISH (HER2, ALK, ROS1, etc.)

Special Instructions: Tumor tissue or biopsy sample required.

Parameters Covered: Specific tumor gene regions.

Report Frequency: 5-10 days

Parameters: Detects gene amplifications, deletions, or translocations associated with breast, lung, brain, and other solid tumors.

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PCR for BCR/ABL1 Quantitative

Special Instructions: Blood or bone marrow sample required.

Parameters Covered: BCR-ABL1 fusion gene.

Report Frequency: 3-5 days

Parameters: Quantitative detection for diagnosis and monitoring of chronic myeloid leukemia (CML).

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PCR for PML/RARA Quantitative

Special Instructions: Blood or bone marrow sample required.

Parameters Covered: PML-RARA fusion gene.

Report Frequency: 3-5 days

Parameters: Used in diagnosis and treatment monitoring of acute promyelocytic leukemia (APML).

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PCR for BRAF, EGFR, JAK2 Mutation

Special Instructions: Blood or tumor tissue sample required.

Parameters Covered: BRAF, EGFR, JAK2 genes.

Report Frequency: 5-7 days

Parameters: Detects key mutations associated with various cancers including melanoma, lung cancer, and leukemia.

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4. Infectious Genetics Testing

Molecular and genetic testing helps in the rapid and accurate detection of infectious diseases for timely treatment.

Covid RT-PCR

Special Instructions: Nasopharyngeal or oropharyngeal swab required.

Parameters Covered: SARS-CoV-2 RNA.

Report Frequency: 24 hours

Parameters: Highly sensitive PCR test to detect active COVID-19 infection.

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Tropical Fever Panel (Dengue/Chikungunya/Malaria)

Special Instructions: Blood sample required.

Parameters Covered: Pathogens causing dengue, chikungunya, and malaria.

Report Frequency: 1-2 days

Parameters: Detects common tropical infections for timely diagnosis and management.

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HBV / HCV / HPV / HIV by PCR

Special Instructions: Blood sample required.

Parameters Covered: Hepatitis B & C, Human Papillomavirus, Human Immunodeficiency Virus.

Report Frequency: 3-5 days

Parameters: PCR-based testing for viral load and infection status in major viral diseases.

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TB-PCR

Special Instructions: Sputum or tissue sample required.

Parameters Covered: Mycobacterium tuberculosis DNA.

Report Frequency: 1-2 days

Parameters: Rapid detection of tuberculosis through PCR amplification of bacterial DNA.

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All Infectious Tests by PCR

Special Instructions: Sample type depends on infection (blood, swab, sputum, tissue).

Parameters Covered: Broad panel of infectious disease pathogens.

Report Frequency: Varies (1–5 days)

Parameters: Comprehensive PCR-based diagnostics for bacterial, viral, and parasitic infections.

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HLA-B27

Special Instructions: Blood sample required.

Parameters Covered: HLA-B27 gene.

Report Frequency: 1-2 days

Parameters: Identifies genetic predisposition to autoimmune and inflammatory conditions like ankylosing spondylitis.

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H1N1 by PCR

Special Instructions: Nasal or throat swab required.

Parameters Covered: H1N1 influenza virus.

Report Frequency: 1-2 days

Parameters: Detects influenza A (H1N1) virus through PCR testing for early management.

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5. Advanced Genomic & Metabolic Testing

Advanced tests provide deeper insights into rare genetic disorders, metabolic conditions, and complete DNA profiling.

Whole Exome Sequencing (WES)

Special Instructions: Blood sample required; genetic counseling recommended.

Parameters Covered: ~20,000 protein-coding genes.

Report Frequency: 4–6 weeks

Parameters: Detects mutations across all protein-coding regions of the genome, useful for rare genetic disorders and unexplained clinical conditions.

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Whole Genome Sequencing (WGS)

Special Instructions: Blood sample required; genetic counseling recommended.

Parameters Covered: Entire genome.

Report Frequency: 6-8 weeks

Parameters: Comprehensive analysis for mutations, structural changes, and variations across the full genome.

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DNA Sequencing (Sanger / NGS)

Special Instructions: Blood sample required; fasting not needed.

Parameters Covered: Single gene or multi-gene panels.

Report Frequency: 7-14 days

Parameters: Detects mutations or variants in specific genes, useful for targeted genetic testing.

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Newborn Screening (Metabolic Panel)

Special Instructions: Heel-prick blood sample within 24-48 hours of birth.

Parameters Covered: Multiple metabolic markers.

Report Frequency: 3-5 days

Parameters: Screens newborns for metabolic disorders like PKU, congenital hypothyroidism, and other inborn errors of metabolism.

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Enzyme Assays

Special Instructions: Blood sample required.

Parameters Covered: Enzyme activity levels.

Report Frequency: 5-7 days

Parameters: Detects enzyme deficiencies associated with rare genetic diseases (e.g., Gaucher disease, Tay-Sachs).

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Protein Electrophoresis / Immunoassays

Special Instructions: Blood sample required.

Parameters Covered: Protein fractions and abnormal proteins.

Report Frequency: 3-5 days

Parameters: Identifies abnormal protein patterns linked to conditions such as sickle cell disease and thalassemia.

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Metabolite Analysis (Tandem Mass Spectrometry)

Special Instructions: Blood or urine sample required.

Parameters Covered: Multiple metabolites.

Report Frequency: 5-7 days

Parameters: Detects abnormal buildup of metabolic products, aiding in the diagnosis of metabolic syndromes.

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