Microarrays allow for the simultaneous analysis of thousands to millions of genetic variations in a single experimAnt. This high-throughput screening capability enables us to quickly identify genetic markers associated with drug response or adverse reactions.
Microarray analysis can identify genetic variations, such as single nucleotide polymorphisms (SNPs), that are associated with drug metabolism, efficacy, toxicity, and adverse reactions. These variations define your unique genetic profile and can serve as biomarkers to predict individual responses to specific drugs, helping in personalized medicine approaches.
By understanding how a patient's genetic profile influences their response to drugs, clinicians can tailor treatments to each individual's genetic profile. This approach, known as precision medicine or personalized medicine, aims to optimize therapeutic outcomes while minimizing adverse effects.
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