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Personal genomics or consumer genetics is the branch of genomics concerned with the sequencing, analysis and interpretation of the genome of an individual. The genotyping stage employs different techniques, including single-nucleotide polymorphism (SNP) analysis chips (typically 0.02% of the genome), or partial or full genome sequencing. Once the genotypes are known, the individual's variations can be compared with the published literature to determine likelihood of trait expression, ancestry inference and disease risk.

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  • Genómica personal (es)
  • 개인 유전체학 (ko)
  • Personal genomics (en)
  • Персональная геномика (ru)
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  • 개인 유전체학은 한 개인의 총 유전체를 해석하고 그에서 파생되는 각종 질병, 노화, 신약개발등을 체학적으로 연구하는 유전체학의 한 분야를 말한다. 개인유전체를 해석할 수 있는 비용이 급속히 떨어짐에 따라, 최근에 크게 대두되고 있는 분야이다. (ko)
  • Персональная геномика является разделом геномики, связанным с секвенированием и анализом генома человека. Стадия генотипирования использует различные методы, включая однонуклеотидно полиморфные (МНП) анализирующие чипы (как правило, составляющие 0,02 % генома), а также частичное или полное секвенирование генома. После расшифровки генотипа его можно проанализировать при помощи опубликованной литературы для определения вероятности риска заболеваний. (ru)
  • La genómica personal es la rama de la genómica que se ocupa de la secuenciación y análisis del genoma de un individuo. La etapa de tipificación del genoma emplea técnicas particulares, incluyendo polimorfismo de nucleótido único (SNP, por sus siglas en inglés) chips de análisis (típicamente 0.02% del genoma), o secuenciación parcial o total del genoma. Una vez los genotipos son conocidos, el genotipo del individuo puede ser comparado con la literatura publicada para determinar la similitud de presencia de características y el riesgo de enfermedad. (es)
  • Personal genomics or consumer genetics is the branch of genomics concerned with the sequencing, analysis and interpretation of the genome of an individual. The genotyping stage employs different techniques, including single-nucleotide polymorphism (SNP) analysis chips (typically 0.02% of the genome), or partial or full genome sequencing. Once the genotypes are known, the individual's variations can be compared with the published literature to determine likelihood of trait expression, ancestry inference and disease risk. (en)
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