DECIPHERING DISEASE WITH PRECISION GENOMICS

Precision genomics is revolutionizing our comprehension of disease. By analyzing an individual's unique genetic makeup, we can pinpoint potential risks and develop customized treatment plans. This approach holds immense potential for enhancing patient outcomes and advancing healthcare into a new era of precision. Through genomic examination, we can

. Such experiments are referred to as mutation accumulation (MA) experiments (Elena and Lenski 2003; Lind and Andersson 2008; Brockhurst et al. 2010). it's now attainable to follow up MA experiments with whole-genome sequencing of the ancestor pressure and its ensuing progeny, Hence enabling with the genome-wide identification with the MA mutations