The sum of all coding regions in a genome is called the exome. In humans, this includes 23,000 genes with approximately 50 million bases. With Whole Exome Sequencing (WES), all exons (protein-coding regions) are analyzed. The genetic testing is therefore focused on the analysis of the 1-2% of the human genome where 85% of known […]
Whole Genome Sequencing (WGS) provides the most comprehensive map of an organism’s genetic make-up. Unlike targeted or exome sequencing, WGS covers all corners of an organisms’ entire genome, which is arguably the most important molecular data.
Because the costs in sequencing are decreasing every day, what we know today of diseases and their relationships with mutations will surely be increased next year, and next, …. That is why for a minimum annual cost, Fullgen offers the service of deep search every year, to verify if new information related to your illness […]
This service applies if you already have your sequence made by another company, and you want our team to recheck in bibliography the mutations found. Our deep search will assure a quality result and that no article related to your mutation is overlooked. If we do not find anything new from the report made by […]
