We are a research-based bioinformatics company focused on deciphering High-throughput sequencing (HTS) data, the genetic codes of the diseases, for precision medicine. We believe in the scientific facts that every individual has the unique genetic codes in the genome. The 4-letter code (A, T, G and C) is the language of genome. The errors in these codes can have serious consequences, such as cancer. These error are called variants or mutations, gene fusions etc. HTS technologies enabled us to find the disease-causing codes at the genome and/or transcriptome levels; therefore, we are focused on deciphering these genetic codes using various bioinformatics approaches. We start from raw sequencing output data and detect mutations, fusions, differentially expressed genes and annotate them for precision medicine.