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 not-to-distant future.

Digital Genome Fingerprinting

A diagnostic test can be performed by a variety of invasive or non-invasive methods. An invasive method involves a surgery or biopsy that is possibly associated with various risks and complications and is usually fairly expensive to perform.

EDGC annotator

EDGC Annotator is an efficient app that annotates functionally genetic variants from human genome by providing information about cancer related variants, genomic regions
allele frequency data, clinical knowledge and insights using ClinVar, OMIM, COSMIC, 1000 Genomes Project allele frequencies, dbSNP and VEP(Variant Effect Predictor) database.

Custom Data Analysis