Technology/Products

Diagnomics on Cloud

Diagnomics-on-Cloud™ is based on a sequencing partnership between Diagnomics and EONE-Diagnomics (EDGC), a certified clinical sequencing laboratory located in Songdo, South-Korea. In the US, Diagnomics has filed for the first US CLIA88-certified NIPT bioinformatics solutions using a secure cloud environment. The NIPT test allows for fast turn-around time, low-cost analysis and has low-input sample requirements.

The NICE® test is a safe, accurate, and easy to perform non-invasive prenatal test. This test can be utilized as early as 10 weeks of gestation time. The results are provided in approximately 10 days from receipt of the sample.

Breast cancer, which ranks at the top of all female cancers, affects 1 in 8 women within their lifetime. Cancer occurs due to environmental and genetic factors, and hereditary cancers account for 5-10% of all cancers

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Analysis platform

Diagnomics-on-Cloud is based on a sequencing partnership between Diagnomics and EONE-Diagnomics (EDGC), a certified clinical sequencing laboratory located in Songdo, South-Korea. In the US, Diagnomics has filed for the first US CLIA88-certified NIPT bioinformatics solutions using a secure cloud environment. The test allows for fast turn-around time, low-cost analysis and low-input sample requirement.

WGS, Exome, Targeted, RNA seq

GSA, Genotyping, CNV, Methylation, Expression

Genotyping, CNV, Expression

Bioinformatics

Diagnomics provides complete personal genome sequencing and bioinformatics solutions to biomedical researchers, physicians, and individuals seeking to understand the roles genes play in personal health and disease. Our vision is to develop complete solutions for personal genome sequencing and annotation, which in turn will enable the sequencing of individual genomes to be part of routine medical care in the near future.

Digital Genome Fingerprinting

Prenatal diagnosis can be performed with a variety of invasive or non-invasive methods. Invasive methods involve a surgery or biopsy that is possibly associated with various risks and complications to mother and fetus and is usually fairly expensive to perform.

EDGC Genomic Annotator

The EDGC Genomic Annotator is an efficient app that annotates functional genetic variants from human genome sequencing data yielding information about cancer genomic variants, allele frequencies, and more. It provides clinical knowledge and is based on databases like ClinVar, OMIM, COSMIC, and the 1000 Genomes Project.

Custom Data Analysis

Variant analysis, RNA seq, CNV analysis, Metagenome, GWAS