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Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays.
Homer, Nils; Szelinger, Szabolcs; Redman, Margot; Duggan, David; Tembe, Waibhav; Muehling, Jill; Pearson, John V; Stephan, Dietrich A; Nelson, Stanley F; Craig, David W.
Afiliação
  • Homer N; Translational Genomics Research Institute, Phoenix, Arizona, United States of America.
PLoS Genet ; 4(8): e1000167, 2008 Aug 29.
Article em En | MEDLINE | ID: mdl-18769715
We use high-density single nucleotide polymorphism (SNP) genotyping microarrays to demonstrate the ability to accurately and robustly determine whether individuals are in a complex genomic DNA mixture. We first develop a theoretical framework for detecting an individual's presence within a mixture, then show, through simulations, the limits associated with our method, and finally demonstrate experimentally the identification of the presence of genomic DNA of specific individuals within a series of highly complex genomic mixtures, including mixtures where an individual contributes less than 0.1% of the total genomic DNA. These findings shift the perceived utility of SNPs for identifying individual trace contributors within a forensics mixture, and suggest future research efforts into assessing the viability of previously sub-optimal DNA sources due to sample contamination. These findings also suggest that composite statistics across cohorts, such as allele frequency or genotype counts, do not mask identity within genome-wide association studies. The implications of these findings are discussed.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise de Sequência com Séries de Oligonucleotídeos / Polimorfismo de Nucleotídeo Único / Genética Médica Tipo de estudo: Clinical_trials / Evaluation_studies / Prognostic_studies Limite: Humans Idioma: En Revista: PLoS Genet Ano de publicação: 2008 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise de Sequência com Séries de Oligonucleotídeos / Polimorfismo de Nucleotídeo Único / Genética Médica Tipo de estudo: Clinical_trials / Evaluation_studies / Prognostic_studies Limite: Humans Idioma: En Revista: PLoS Genet Ano de publicação: 2008 Tipo de documento: Article