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  "documentTitle": "23andMe | Investor Day Presentation Deck | 78 slides",
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  "presentationDate": "2022-01-01 00:00:00",
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  "notes": "Includes a visual process diagram of imputation and a before/after Manhattan plot comparison.",
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      "text": "We type ~650,000 SNPs using our genotyping array, which allows accurate imputation for >35m SNPs in the genome.",
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      "text": "Whole-genome sequencing ~$1000 / sample. Exome sequencing ~$400 / sample. Imputation < $0.01 / sample",
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      "text": "Nearby genetic variants are correlated with each other. Knowing the variants one position allows the nearby variants to be inferred. E.g. Fill in the blanks: The q***k brown f*x jumps ov*r the **zy dog. The same principle applies in genetics. The process of filling in the gaps is known as ‘genotype imputation’.",
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