The goal of SD Genomics is to contribute to improvement of global health of the world.
SD Genomics has 5 professional bioinformaticians and 1 MD who has vast experiences of providing genetic counselling will decode the complex genomic information for the as clinical level. We now mainly provide clinical diagnostic NGS services all over the world.
Whole Exome Sequencing for clinical purpose.
BRCACancer discovery is a NGS (next generation sequencing) based test for BRCA1 and BRCA2
genes, that are associated with Hereditary Breast and Ovarian Cancer Syndrome.²
To find the variants at a high sensitivity, the test is performed to have an average of 500x read of depth and 99.9% of the bases have at least 30x reads of depth.
The price is including clinical genetic report technically described by Medical Doctor.
Biochemistry & Molecular Biology Services
Biostatistics & Bioinformatics Services
Clinical Molecular Diagnostics Services
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