Researchers have discovered that mutations in DNA that are not revealed in whole exome sequencing can impact gene function, protein synthesis, and result in hereditary diseases. WGS, sometimes referred to as complete genome sequencing, can identify differences in any region of the genome at one time and establish the sequence of every nucleotide in a person's DNA. 

Creative Biolabs supports researchers worldwide with their genome sequencing needs by utilizing the cutting edge SuPrecisionTM platform. These are just a few of the services we offer: 1) whole genome re-sequencing; 2) somatic variant identification; 3) germline variant detection; 4) De novo genome assembly; 5) copy number variation; and 6) structural variant discovery.