

GeneTech’s NGS Lab uses advanced platforms like Ion Torrent, Illumina, and MGI DNBSEQ for Whole Exome, Genome, and Targeted Sequencing—delivering high-quality, fast results. It also features CytoScan GCS 3000 and GeneTitan MC FastScan for microarray and SNP genotyping, processing thousands of samples monthly.

List of labs at GeneTech - Next Generation Sequencing (NGS) Lab, Cyto Microarray Lab, SNP Genotyping Lab, DNA and RNA Extraction Lab, PCR and qPCR Lab, LibPrep Lab, Sample Prep Lab, Sanger Lab, Gel Doc Lab, Image Analysis Lab, CytoGenetics Lab, FISH Lab, Prenatal Culture Lab, Biochem Lab, Reporting Lab, Lab Inventory Room, Sterilization Faciltiies. For Patient Services -- Genetic Counseling rooms, Ultrasound Facility with Recovery Area, Sample Collection Facilties, Report Delivery Area. GeneTech also has a large seminar hall and a conference hall where meetings and workshops are conducted for physicians and agri specialists.
GeneTech’s Next-Generation Sequencing Lab is equipped with multiple platforms—including Thermo Fisher’s Ion Torrent S5 and Ion Torrent S5 Prime, Illumina, and MGI’s DNBSEQ with MegaBOLT—enabling a wide range of sequencing applications, such as Whole Exome Sequencing, Low-Pass Whole Genome Sequencing, and Targeted Sequencing. These deliver exceptional quality, high throughput, and rapid turnaround times.
GeneTech utilizes Affymetrix’s CytoScan GCS 3000 for cytogenomic microarray processing and the GeneTitan MC FastScan for SNP genotyping, supported by all necessary ancillary equipment to handle thousands of samples per month.
















Next Generation Sequencing (NGS) Lab uses advanced genetic technology to analyze DNA and RNA with high speed and accuracy. It helps in disease diagnosis, personalized medicine, and research by providing deep insights into genetic information.

SNP Array Lab specializes in detecting genetic variations across the genome. It identifies single nucleotide polymorphisms (SNPs) to study genetic traits, diseases, and ancestry with high accuracy and efficiency.

CytoMicroarray Lab analyzes chromosomes at a molecular level to detect genetic abnormalities. It helps identify deletions, duplications, and other chromosomal changes linked to developmental disorders and genetic diseases.

Sanger Sequencing Lab provides precise DNA sequencing using the classic chain-termination method. It’s ideal for validating genetic variants, small-scale studies, and clinical diagnostics with high accuracy and reliability.

Gel Documentation Lab captures and analyzes images of DNA, RNA, or protein gels. It ensures accurate visualization and documentation of electrophoresis results for research, diagnostics, and quality control.

PCR and qPCR Lab amplifies and quantifies DNA or RNA to study genes and detect diseases. It provides fast, accurate results for diagnostics, genetic research, and molecular biology studies.

LibPrep Lab prepares high-quality DNA or RNA libraries for sequencing. It ensures accurate sample processing, enabling reliable results in genomics, transcriptomics, and other molecular research applications.

DNA and RNA Extraction Lab isolates pure genetic material from biological samples. It ensures high-quality DNA and RNA for use in sequencing, PCR, and other molecular biology applications.

Cytogenetics Lab studies chromosomes to detect genetic abnormalities and chromosomal disorders. It plays a key role in diagnosing cancers, infertility, and developmental conditions through karyotyping and other advanced techniques.

Prenatal Culture Lab grows and analyzes fetal cells to detect genetic or chromosomal abnormalities early in pregnancy. It helps in assessing fetal health and guiding clinical decisions.

Biochem Lab analyzes blood, urine, and other body fluids to assess metabolic and biochemical health. It helps in diagnosing diseases, monitoring organ function, and guiding treatment plans.

FISH Lab (Fluorescence In Situ Hybridization) detects specific DNA sequences on chromosomes using fluorescent probes. It helps identify genetic abnormalities, cancers, and chromosomal disorders quickly and accurately.

Image Analysis Lab processes and interprets scientific images, such as gels, cells, or tissues. It provides precise data for research, diagnostics, and quality control in molecular and cellular studies.

Incubation Lab provides controlled environments for growing cells, tissues, or microbes. It ensures optimal conditions for research, diagnostics, and experimental studies in biology and medicine.

Biochemical Lab studies chemical processes in the body by analyzing enzymes, proteins, and metabolites. It helps in diagnosing diseases, monitoring health, and supporting medical research.

Next Generation Sequencing (NGS) Lab uses advanced genetic technology to analyze DNA and RNA with high speed and accuracy. It helps in disease diagnosis, personalized medicine, and research by providing deep insights into genetic information.

SNP Array Lab specializes in detecting genetic variations across the genome. It identifies single nucleotide polymorphisms (SNPs) to study genetic traits, diseases, and ancestry with high accuracy and efficiency.

CytoMicroarray Lab analyzes chromosomes at a molecular level to detect genetic abnormalities. It helps identify deletions, duplications, and other chromosomal changes linked to developmental disorders and genetic diseases.

Sanger Sequencing Lab provides precise DNA sequencing using the classic chain-termination method. It’s ideal for validating genetic variants, small-scale studies, and clinical diagnostics with high accuracy and reliability.

Gel Documentation Lab captures and analyzes images of DNA, RNA, or protein gels. It ensures accurate visualization and documentation of electrophoresis results for research, diagnostics, and quality control.

PCR and qPCR Lab amplifies and quantifies DNA or RNA to study genes and detect diseases. It provides fast, accurate results for diagnostics, genetic research, and molecular biology studies.

LibPrep Lab prepares high-quality DNA or RNA libraries for sequencing. It ensures accurate sample processing, enabling reliable results in genomics, transcriptomics, and other molecular research applications.

DNA and RNA Extraction Lab isolates pure genetic material from biological samples. It ensures high-quality DNA and RNA for use in sequencing, PCR, and other molecular biology applications.

Cytogenetics Lab studies chromosomes to detect genetic abnormalities and chromosomal disorders. It plays a key role in diagnosing cancers, infertility, and developmental conditions through karyotyping and other advanced techniques.

Prenatal Culture Lab grows and analyzes fetal cells to detect genetic or chromosomal abnormalities early in pregnancy. It helps in assessing fetal health and guiding clinical decisions.

Biochem Lab analyzes blood, urine, and other body fluids to assess metabolic and biochemical health. It helps in diagnosing diseases, monitoring organ function, and guiding treatment plans.

FISH Lab (Fluorescence In Situ Hybridization) detects specific DNA sequences on chromosomes using fluorescent probes. It helps identify genetic abnormalities, cancers, and chromosomal disorders quickly and accurately.

Image Analysis Lab processes and interprets scientific images, such as gels, cells, or tissues. It provides precise data for research, diagnostics, and quality control in molecular and cellular studies.

Incubation Lab provides controlled environments for growing cells, tissues, or microbes. It ensures optimal conditions for research, diagnostics, and experimental studies in biology and medicine.