Implications it has for our health that we now have the complete sequence of the genome? The new version of the human genome is a springboard towards the well-known " precision medicine ". The goal is to individualize treatments for each patient. In addition, it will allow an improvement in diagnostic tools for those diseases with a genetic basis (from developmental problems to cancers). Although there have already been advances in the treatment of some diseases with the “old” genome (crch30), much more can now be fine-tuned.
Thus, the drugs will be aimed at those individuals with a specific genetic configuration. Hence the importance of analyzing variability, since designing a safe and effective drug for each and every one of the individuals is impossible. Thus, with the latest complete fax number list version of the genome, therapeutic targets will be described by the specific genomic configuration of population sectors that share certain characteristics at the molecular level.
Future prospects: collecting human genetic diversity like the previous genome (whose assembly was achieved from the analysis of the genome of 60 people), the current one does not show individual genetic diversity either. That is, t2t-chm13 is "a" complete human genome and not "the" complete human genome. Therefore, the next great challenge is to achieve a genome that represents all human genetic variation. A titanic task because, with all certainty, there will be hundreds or thousands of genomes. However, analyzing its complex details will be the key that makes us different as individuals. The first step to