At Alfalah Lahore Lab, our Molecular Genetics Department is committed to providing advanced molecular diagnosis and genetic screening across all age groups. We cater to individuals with known genetic disorders and those seeking proactive health assessments. Additionally, we offer opportunities for training and research in this cutting-edge field.
Our department specializes in the latest molecular technologies, offering a wide range of services, including:
- Screening for chromosomal abnormalities
- Detection of pathogenic mutations in single-gene disorders
- Identification of disease-related mutations through targeted gene panels and comprehensive genome or exome analysis
Our lab employs the following advanced technologies to deliver accurate results:
- Next Generation Sequencing (NGS)
- Sanger DNA Sequencing
- Real-Time PCR (RT-PCR)
- End Point PCR
- Karyotyping and Cytogenetic Analysis
- Fluorescent In-situ Hybridization (FISH)
- Reverse Sequence Specific Oligonucleotide Polymerase Chain Reaction (RSSO PCR
Our department offers a broad range of molecular genetic analyses, including:
- BCR-ABL Quantitation by PCR
- JAK-2 Mutation Detection by PCR
- HLA Allele Detection by PCR
- EGFR Gene Mutation Analysis
- PIK3CA Gene Mutation Analysis
- Beta Thalassemia Gene Sequencing
- CFTR Mutation Detection for Cystic Fibrosis
- HLA DQ2 & DQ8 Detection for Celiac Disease
- HTT Genetic Analysis for Huntington’s Disease
- SMN Genetic Analysis for Spinal Muscular Atrophy (SMA)
- BRCA1/2 Genetic Analysis by Next Generation Sequencing
- Cancer Hotspot Genetic Analysis by Next Generation Sequencing
At Alfalah Lahore Lab, we are continually expanding our molecular genetics testing capabilities, ensuring that we remain at the forefront of genetic diagnostics.

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