Genotyping for the Masses

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Experts agree that the ideal way to study each person’s differences from one another — and to figure out how those differences relate in terms of disease — is to fully sequence each individual’s genome and use that as the foundation for tracking variation. But it’s a long way off before sequencing is cheap enough to make that scenario feasible. Good thing, then, that advances are still being made in the SNP genotyping domain.

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