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Statements

Subject Item
dbr:Personal_genomics
rdf:type
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rdfs:label
개인 유전체학 Genómica personal Персональная геномика Personal genomics
rdfs:comment
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. 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. 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. 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.
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dbr:Full_genome_sequencing dbr:Genealogy dbr:Crowd_sourced dbr:Genetic_Genealogy dbr:Murders_of_Jay_Cook_and_Tanya_Van_Cuylenborg dbr:Joseph_James_DeAngelo dbr:ABI_SOLiD dbr:National_Cancer_Institute dbr:DNA.land dbr:Manuel_Corpas_(Scientist) dbr:Human_genome dbr:Gattaca dbr:Pharmacogenomics dbr:Personalized_medicine dbr:Human_Genome dbr:Whole_exome_sequencing dbr:Complete_Genomics dbr:Full_Genome_Sequencing dbr:Genotype dbr:Genomics dbr:Branch dbr:Brigham_and_Women's_Hospital dbr:Genetic_Information_Nondiscrimination_Act dbr:Exome dbr:Lyle_Stevik dbr:Personal_Genome_Project dbr:OpenSNP dbr:Perfect_DNA dbr:National_Institutes_of_Health dbr:Genotyping dbr:Sequencing dbr:Applied_Biosystems dbr:Citizen_science dbr:Predictive_medicine dbr:FamilyTreeDNA dbr:Genome-wide_association_studies dbr:GEDmatch dbr:NHGRI dbr:Joseph_Newton_Chandler_III dbr:Variants_of_unknown_significance dbr:Multifactorial_inheritance dbr:Robert_C._Green dbr:Illumina_(company) dbr:Genetic_disorders dbr:Personal_Genetics_Education_Project n15:From_spit_to_DNA-sample.webm dbr:Mountain_View,_California n15:Cost_per_Genome.png dbr:Common_Rule dbr:Rare_disease dbr:Single-nucleotide_polymorphism dbr:Ancestry dbr:Murder_of_Marcia_King dbr:East_Area_Rapist dbr:Tay_Sachs_Disease dbr:PubMed dbr:Dor_Yeshorim dbr:Knome dbr:New_York_Genome_Center dbr:DNA_sequencing dbc:Genomics dbr:Harvard_Medical_School dbr:Base_pair dbr:Smithsonian dbr:$1,000_genome dbr:Polymorphism_(biology) dbr:Pharmacogenetics dbr:Oncogenomics dbr:Bioinformatics dbr:Precision_medicine dbr:Crowd_sourcing dbr:Genetic_discrimination
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dbo:abstract
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. Automated high-throughput sequencers have increased the speed and reduced the cost of sequencing, making it possible to offer whole genome sequencing including interpretation to consumers since 2015 for less than $1,000. The emerging market of direct-to-consumer genome sequencing services has brought new questions about both the medical efficacy and the ethical dilemmas associated with widespread knowledge of individual genetic information. 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. 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. Los secuenciadores automáticos han aumentado la velocidad y reducido el costo de secuenciación, volviéndolo viable para ofrecer exámenes genéticos a los consumidores. 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.
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