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Journal Abstract Search

117 related items for PubMed ID: 19083859

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  • 3. Evaluation of the iPLEX® Sample ID Plus Panel designed for the Sequenom MassARRAY® system. A SNP typing assay developed for human identification and sample tracking based on the SNPforID panel.
    Johansen P, Andersen JD, Børsting C, Morling N.
    Forensic Sci Int Genet; 2013 Sep; 7(5):482-7. PubMed ID: 23948317
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  • 5. Forensic typing of autosomal SNPs with a 29 SNP-multiplex--results of a collaborative EDNAP exercise.
    Sanchez JJ, Børsting C, Balogh K, Berger B, Bogus M, Butler JM, Carracedo A, Court DS, Dixon LA, Filipović B, Fondevila M, Gill P, Harrison CD, Hohoff C, Huel R, Ludes B, Parson W, Parsons TJ, Petkovski E, Phillips C, Schmitter H, Schneider PM, Vallone PM, Morling N.
    Forensic Sci Int Genet; 2008 Jun; 2(3):176-83. PubMed ID: 19083818
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  • 9. Single nucleotide polymorphism typing with massively parallel sequencing for human identification.
    Seo SB, King JL, Warshauer DH, Davis CP, Ge J, Budowle B.
    Int J Legal Med; 2013 Nov; 127(6):1079-86. PubMed ID: 23736940
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  • 10. Forensically relevant SNaPshot® assays for human DNA SNP analysis: a review.
    Mehta B, Daniel R, Phillips C, McNevin D.
    Int J Legal Med; 2017 Jan; 131(1):21-37. PubMed ID: 27841004
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  • 15. Analysis of four PCR/SNaPshot multiplex assays analyzing 52 SNPforID markers.
    Goodwin W, Alimat S.
    Electrophoresis; 2017 Apr; 38(7):1007-1015. PubMed ID: 28008628
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  • 16. A 21-locus autosomal SNP multiplex and its application in forensic science.
    Hou G, Jiang X, Yang Y, Jia F, Li Q, Zhao J, Guo F, Liu L.
    J Forensic Sci; 2014 Jan; 59(1):5-14. PubMed ID: 24400826
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  • 17. A novel multiplex assay of SNP-STR markers for forensic purpose.
    Wei T, Liao F, Wang Y, Pan C, Xiao C, Huang D.
    PLoS One; 2018 Jan; 13(7):e0200700. PubMed ID: 30020969
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  • 18. A SNaPshot assay for genotyping 44 individual identification single nucleotide polymorphisms.
    Lou C, Cong B, Li S, Fu L, Zhang X, Feng T, Su S, Ma C, Yu F, Ye J, Pei L.
    Electrophoresis; 2011 Feb; 32(3-4):368-78. PubMed ID: 21298663
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  • 19. A rare mutation in the primer binding region of the Amelogenin X homologue gene.
    Maciejewska A, Pawłowski R.
    Forensic Sci Int Genet; 2009 Sep; 3(4):265-7. PubMed ID: 19647713
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  • 20. 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.
    Børsting C, Rockenbauer E, Morling N.
    Forensic Sci Int Genet; 2009 Dec; 4(1):34-42. PubMed ID: 19948332
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