Literature DB >> 20650697

Autosomal SNP typing of forensic samples with the GenPlex™ HID System: results of a collaborative study.

C Tomas1, G Axler-DiPerte, Z M Budimlija, C Børsting, M D Coble, A E Decker, A Eisenberg, R Fang, M Fondevila, S Frisk Fredslund, S Gonzalez, A J Hansen, P Hoff-Olsen, C Haas, P Kohler, A K Kriegel, B Lindblom, F Manohar, O Maroñas, H S Mogensen, K Neureuther, H Nilsson, M K Scheible, P M Schneider, M L Sonntag, M Stangegaard, D Syndercombe-Court, C R Thacker, P M Vallone, A A Westen, N Morling.   

Abstract

The GenPlex™ HID System (Applied Biosystems - AB) offers typing of 48 of the 52 SNPforID SNPs and amelogenin. Previous studies have shown a high reproducibility of the GenPlex™ HID System using 250-500pg DNA of good quality. An international exercise was performed by 14 laboratories (9 in Europe and 5 in the US) in order to test the robustness and reliability of the GenPlex™ HID System on forensic samples. Three samples with partly degraded DNA and 10 samples with low amounts of DNA were analyzed in duplicates using various amounts of DNA. In order to compare the performance of the GenPlex™ HID System with the most commonly used STR kits, 500pg of partly degraded DNA from three samples was typed by the laboratories using one or more STR kits. The median SNP typing success rate was 92.3% with 500pg of partly degraded DNA. Three of the fourteen laboratories counted for more than two thirds of the locus dropouts. The median percentage of discrepant results was 0.2% with 500pg degraded DNA. An increasing percentage of locus dropouts and discrepant results were observed when lower amounts of DNA were used. Different success rates were observed for the various SNPs. The rs763869 SNP was the least successful. With the exception of the MiniFiler™ kit (AB), GenPlex™ HID performed better than five other tested STR kits. When partly degraded DNA was analyzed, GenPlex™ HID showed a very low mean mach probability, while all STR kits except MiniFiler™ had very limited discriminatory power.
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 20650697     DOI: 10.1016/j.fsigen.2010.06.007

Source DB:  PubMed          Journal:  Forensic Sci Int Genet        ISSN: 1872-4973            Impact factor:   4.882


  4 in total

1.  Single nucleotide polymorphism typing with massively parallel sequencing for human identification.

Authors:  Seung Bum Seo; Jonathan L King; David H Warshauer; Carey P Davis; Jianye Ge; Bruce Budowle
Journal:  Int J Legal Med       Date:  2013-06-05       Impact factor: 2.686

2.  Massively parallel sequencing of forensically relevant single nucleotide polymorphisms using TruSeq™ forensic amplicon.

Authors:  David H Warshauer; Carey P Davis; Cydne Holt; Yonmee Han; Paulina Walichiewicz; Tom Richardson; Kathryn Stephens; Anne Jager; Jonathan King; Bruce Budowle
Journal:  Int J Legal Med       Date:  2014-11-19       Impact factor: 2.686

3.  Kinship Analysis with Diallelic SNPs - Experiences with the SNPforID Multiplex in an ISO17025 Accreditated Laboratory.

Authors:  Claus Børsting; Martin Mikkelsen; Niels Morling
Journal:  Transfus Med Hemother       Date:  2012-05-12       Impact factor: 3.747

4.  TIA: algorithms for development of identity-linked SNP islands for analysis by massively parallel DNA sequencing.

Authors:  M Heath Farris; Andrew R Scott; Pamela A Texter; Marta Bartlett; Patricia Coleman; David Masters
Journal:  BMC Bioinformatics       Date:  2018-04-11       Impact factor: 3.169

  4 in total

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