- sakkthi@gmail.com
- Mon - Sun: 8.00 am - 7.00 pm
- Opp. G.H. Near Anusha Hospital, Erode - 09.
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411 University St, Seattle, USA
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+1 -800-456-478-23
At Sakkthi Clinical Laboratory (SCL), our Genomics services provide advanced genome-wide analysis to understand genetic predispositions, inherited disorders, and complex diseases. By decoding the genome, we enable personalized healthcare, early disease detection, and targeted therapy, empowering clinicians and patients to make informed decisions.
Genomics is the study of the entire set of genes (the genome) in an individual. It goes beyond single-gene analysis, providing insights into how genes interact, influence health, and contribute to disease risk.
Genomics testing is especially valuable for:
Individuals with a family history of genetic disorders
High-risk pregnancies and prenatal health screening
Patients with cancer or complex diseases
Research and personalized medicine initiatives
Early detection and prevention of inherited and multifactorial conditions
Whole Genome Sequencing (WGS)
Comprehensive sequencing of the entire genome
Identifies inherited mutations, structural variants, and rare disorders
Whole Exome Sequencing (WES)
Focused analysis of coding regions of genes
Detects disease-causing variants with high accuracy
Targeted Gene Panels
Analysis of specific gene groups linked to hereditary conditions or cancers
Offers rapid and precise diagnostics for focused clinical concerns
Pharmacogenomics
Evaluates genetic variations that affect drug metabolism and response
Supports personalized treatment planning and dosage optimization
Genomic Data Analysis & Interpretation
Advanced bioinformatics pipelines for accurate variant calling and risk assessment
Reports actionable insights for clinicians and genetic counselors
Research & Translational Genomics
Supports clinical trials, population studies, and genomic research
Enables the development of precision medicine strategies