Decodes 100% of your DNA across 3.2 billion base pairs
Clinical-grade 30x depth of coverage using Next-Generation Sequencing (NGS)
Covers hereditary disease risks, cancer screening, pharmacogenomics, carrier status, and wellness traits
NABL-accredited laboratory (MC-6120) with strict quality controls
Includes expert genetic counselling session post-report
Bank-level data encryption — your data is never shared or sold
Available with or without raw genomic data (FASTQ, BAM, VCF files)
Hereditary Disease Risk Panel
Hereditary Cancer Screening Panel
Pharmacogenomics (Drug Response) Panel
Carrier Screening Panel
Wellness & Traits Panel
Ancestry & Haplogroup Analysis
Whole Genome Sequencing (WGS) using Illumina Next-Generation Sequencing (NGS) platforms at 30x depth of coverage. Reads all 3.2 billion base pairs across both coding (exons) and non-coding (introns) regions of the genome. Processed in an NABL-accredited genomics facility (MC-6120) under strict quality controls.