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Genetic polymorphisms of 9 non-combined of DNA index system short tandem repeat loci in Guangdong Han population / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 580-584, 2009.
Artigo em Chinês | WPRIM | ID: wpr-287369
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the genetic polymorphisms and their forensic application of 9 non-combined of DNA index system (CODIS) short tandem repeat(STR) loci in Guangdong Han population.</p><p><b>METHODS</b>DNA samples from 500 unrelated individuals were extracted and amplified with fluorescence labeled multiplex PCR system. PCR products were separated and genotyped with capillary electrophoresis.</p><p><b>RESULTS</b>One hundred and fifteen alleles and 160 genotypes were observed in the 9 STR loci, respectively. The heterozygosity was 0.824-0.884, the discrimination power (DP) was 0.925-0.969 and the polymorphism information content (PIC) was 0.77-0.86, respectively. The distribution met the Hardy-Weinberg equilibrium (P > 0.05). The total discrimination power was 1.00 x 10(-13), the combined probability of exclusion for trio-paternity testing was 0.999989488. The combined probability of exclusion for duo-paternity testing was 0.873436.</p><p><b>CONCLUSION</b>The 9 STR loci are powerful and reliable for personal identification and paternity testing. They can be used as supplementary loci in fatherless (motherless) testing or cases with mutation events.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Polimorfismo Genético / China / Repetições de Microssatélites / Povo Asiático / Alelos / Etnologia / Genética / Genótipo Limite: Humanos País/Região como assunto: Ásia Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2009 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Polimorfismo Genético / China / Repetições de Microssatélites / Povo Asiático / Alelos / Etnologia / Genética / Genótipo Limite: Humanos País/Região como assunto: Ásia Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2009 Tipo de documento: Artigo