ArticleInternational journal of legal medicine2011
Fourteen non-CODIS autosomal short tandem repeat loci multiplex data from Taiwanese.
Article in International journal of legal medicine, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed.
- Population data of 13 nonCODIS STR markers located inside the 6 nonsyndromic oculocutaneous albinism genes.International journal of legal medicine · 2016Article
- Identification and characterization of the highly polymorphic locus D14S739 in the Han Chinese population.Croatian medical journal · 2015Article
- Assessment of application value of 19 autosomal short tandem repeat loci of GoldenEye 20A kit in forensic paternity testing.International journal of legal medicine · 2013Article
- Substitution mutation induced migration anomaly of a D10S2325 allele on capillary electrophoresis.International journal of legal medicine · 2013Article
- Heterozygosity assessment of five STR loci located at 5q13 region for preimplantation genetic diagnosis of spinal muscular atrophy.Molecular biology reports · 2013Article
- Population data of 21 non-CODIS STR loci in Han population of northern China.International journal of legal medicine · 2012Article
- Fifteen non-CODIS autosomal short tandem repeat loci multiplex data from nine population groups living in Taiwan.International journal of legal medicine · 2012Article
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7 authors.
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Abstract
Interest in the development of polymorphic short tandem repeat (STR) markers unlinked to the CODIS loci is growing among forensic practitioners. We developed a multiplex system in which14 autosomal STR (D3S1744, D4S2366, D8S1110, D12S1090, D13S765, D14S608, Penta E, D17S1294, D18S536, D18S1270, D20S470, D21S1437, Penta D, and D22S683) could be amplified in one single polymerase chain reaction. DNA samples from 572 unrelated Taiwanese Han subjects were analyzed using this 14 STR multiplex system. Thirty parent-child pairs of parentage testing cases with a combined paternity index (CPI) below 1,000 and 32 parent-child pairs with single-step mutations found in AmpFℓSTR Identifiler loci were also recruited for validation of the newly developed system. DNA sequencing was performed for novel STRs and novel alleles found in these subjects. The distributions of allelic frequencies for these autosomal STRs and sequence data, allele nomenclature for the STRs, and forensic parameters are presented. The discrimination power in our multiplex loci ranged from 0.6858 (D18S536) to 0.9168 (Penta E), with a combined discrimination power of 0.999999999. It provides additional power to distinguish the possible single-step mutations in parent-child pairs and improves the ability to prove parentage by increasing the CPI. The combined power of exclusion of these 14 loci in Taiwanese Han in this study was 0.9999995913. In conclusion, this 14-autosomal STRs multiplex system provides highly informative STR data and appears useful in forensic casework and parentage testing.
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