Forensic Science International: Genetics
Volume 5, Issue 3 , Pages e81-e82 , June 2011

SNP typing of the reference materials SRM 2391b 1–10, K562, XY1, XX74, and 007 with the SNPforID multiplex

Received 19 July 2010

References 

  1. Sanchez JJ, Phillips C, Børsting C, Balogh K, Bogus M, Fondevila M, et al. A multiplex assay with 52 single nucleotide polymorphisms for human identification. Electrophoresis. 2006;27:1713–1724
  2. Børsting C, Rockenbauer E, Morling N. Validation of a single nucleotide polymorphism (SNP) typing assay with 49 SNPs for forensic genetic testing in a laboratory accredited according to the ISO 17025 standard. Forensic Sci. Int. Genet. 2009;4:34–42
  3. Porras L, Phillips C, Fondevila M, Beltrán L, Ortiz T, Rondon F, et al. Genetic variability of the SNPforID 52-plex identification-SNP panel in Central West Columbia. Forensic Sci. Int. Genet. 2009;4:e9–10
  4. Drobnic K, Børsting C, Rockenbauer E, Tomas C, Morling N. Typing of 49 autosomal SNPs by SNaPshot® in the Slovenian population. Forensic Sci. Int. Genet. 2010;
  5. Santos C, Phillips C, Fondevila M, Porras-Hurtado L, Carrecedo A, Souto L, et al. A study of East Tumor variability using the SNPforID 52-plex SNP panel. Forensic Sci. Int. Genet. 2010;
  6. Amigo J, Phillips C, Lareu MV, Carrecedo A. The SNPforID browser: an online tool for query and display of frequency data from the SNPforID project. Int. J. Legal Med. 2008;122:435–440
  7. Philips C, Fang R, Ballard D, Fondevila M, Harrison C, Hyland F, et al. Evaluation of the Genplex SNP typing system and a 49-plex forensic marker panel. Forensic Sci. Int. Genet. 2007;1:180–185
  8. Stangegaard M, Tomas C, Hansen AJ, Frank-Hansen R, Børsting C, Morling N. Biomek®-3000 and GenPlex SNP genotyping in forensic genetics. JALA. 2008;13:297–303
  9. Tomas C, Stangegaard M, Børsting C, Hansen AJ, Morling N. Typing of 48 autosomal SNPs and amelogenin with GenPlex SNP genotyping system in forensic genetics. Forensic Sci. Int. Genet. 2008;3:1–6
  10. Musgrave-Brown E, Ballard D, Balogh K, Bender K, Berger B, Bogus M, et al. Forensic validation of the SNPfor ID 52-plex assay. Forensic Sci. Int. Genet. 2007;1:186–190
  11. Sanchez JJ, Bųrsting C, Balogh K, Berger B, Bogus M, Butler J, et al. Forensic typing of autosomal SNPs with a 29 SNP-multiplex—results of a collaborative EDNAP exercise. Forensic Sci. Int. Genet. 2008;2:176–183
  12. Tomas C, Axler-DiPerte G, Budimlija ZM, Børsting C, Coble MD, Decker AE, et al. Autosomal SNP typing of forensic samples with the GenPlex™ HID System: results of a collaborative study. Forensic Sci. Int. Genet. 2010;
  13. Phillips C, Fondevila M, Garcia-Magariños M, Rodriguez A, Salas A, Carrecedo A, et al. Resolving relationship tests that show ambiguous STR results using autosomal SNPs as supplementary markers. Forensic Sci. Int. Genet. 2008;2:198–204
  14. Børsting C, Sanchez JJ, Hansen HE, Hansen AJ, Bruun HQ, Morling N. Performance of the SNPforID 52 SNP-plex assay in paternity testing. Forensic Sci. Int. Genet. 2008;2:292–300
  15. Børsting C, Morling N. Mutations and/or relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers. Forensic Sci. Int. Genet. 2010;
  16. Tomas C, Sanchez JJ, Castro JA, Børsting C, Morling N. Forensic usefulness of a 25 X-chromosome SNP marker set. Transfusion. 2010;
  17. Fondevila M, Phillips C, Naveran N, Fernandez L, Cerezo M, Salas A, et al. Case report: identification of skeletal remains using short-amplicon marker analysis of severely degraded DNA extracted from a decomposed and charred femur. Forensic Sci. Int. Genet. 2008;2:212–218
  18. Schneider PM. Scientific standards for studies in forensic genetics. Forensic Sci. Int. 2007;165:238–243

PII: S1872-4973(10)00115-8

doi: 10.1016/j.fsigen.2010.07.004

Forensic Science International: Genetics
Volume 5, Issue 3 , Pages e81-e82 , June 2011

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