DECIPHERING DISEASE WITH PRECISION GENOMICS

Precision genomics is revolutionizing our perception of disease. By analyzing an individual's unique genetic makeup, we can detect potential risks and develop personalized treatment plans. This strategy holds immense potential for enhancing patient outcomes and propelling healthcare into a new era of specificity. Through genomic examination, we can

Most human cells have 23 pairs of chromosomes. One chromosome of each pair is inherited from an individual’s mom, and the opposite comes from their father. This is why children are inclined to look like their moms and dads, and why they may have a bent to develop selected diseases that operate within their families. I must also mention that the