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This application focuses on the strategic selection of single nucleotide polymorphisms (SNPs) to improve the accuracy and reliability of association studies in genetics. By employing innovative methodologies to identify and prioritize SNPs, researchers can uncover meaningful genetic associations with complex traits and diseases. This tool aids in streamlining the analytic process, enhances data interpretation, and facilitates better understanding of genetic influences, ultimately contributing to advancements in personalized medicine and public health.
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