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Volumn 5, Issue 3, 2011, Pages

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

Author keywords

Forensic genetics; Reference DNA samples; Single nucleotide polymorphism; SNPforID multiplex

Indexed keywords

DNA;

EID: 79953850336     PISSN: 18724973     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fsigen.2010.07.004     Document Type: Letter
Times cited : (9)

References (18)
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    • 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
    • C. Børsting, E. Rockenbauer, N. Morling, 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. 4 (2009) 34-42.
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    • Børsting, C.1    Rockenbauer, E.2    Morling, N.3
  • 6
    • 50849137155 scopus 로고    scopus 로고
    • The SNPforID browser: An online tool for query and display of frequency data from the SNPforID project
    • J. Amigo, C. Phillips, M.V. Lareu, A. Carrecedo, The SNPforID browser: an online tool for query and display of frequency data from the SNPforID project, Int. J. Legal Med. 122 (2008) 435-440.
    • (2008) Int. J. Legal Med. , vol.122 , pp. 435-440
    • Amigo, J.1    Phillips, C.2    Lareu, M.V.3    Carrecedo, A.4
  • 9
    • 56549084702 scopus 로고    scopus 로고
    • Typing of 48 autosomal SNPs and amelogenin with GenPlex SNP genotyping system in forensic genetics
    • C. Tomas, M. Stangegaard, C. Børsting, A.J. Hansen, N. Morling, Typing of 48 autosomal SNPs and amelogenin with GenPlex SNP genotyping system in forensic genetics, Forensic Sci. Int. Genet. 3 (2008) 1-6.
    • (2008) Forensic Sci. Int. Genet. , vol.3 , pp. 1-6
    • Tomas, C.1    Stangegaard, M.2    Børsting, C.3    Hansen, A.J.4    Morling, N.5
  • 15
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    • Mutations and/or relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers
    • doi:10.1016/j.fsigen.2010.02.007
    • C. Børsting, N. Morling, Mutations and/or relatives? Six case work examples where 49 autosomal SNPs were used as supplementary markers, Forensic Sci. Int. Genet. (2010), doi:10.1016/j.fsigen.2010.02.007.
    • (2010) Forensic Sci. Int. Genet.
    • Børsting, C.1    Morling, N.2
  • 16
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    • Forensic usefulness of a 25 X-chromosome SNP marker set
    • doi:10.1111/j.1537-2995.2010.02696.x
    • C. Tomas, J.J. Sanchez, J.A. Castro, C. Børsting, N. Morling, Forensic usefulness of a 25 X-chromosome SNP marker set, Transfusion (2010), doi:10.1111/j.1537-2995.2010.02696.x.
    • (2010) Transfusion
    • Tomas, C.1    Sanchez, J.J.2    Castro, J.A.3    Børsting, C.4    Morling, N.5
  • 17
    • 43049088159 scopus 로고    scopus 로고
    • Case report: Identification of skeletal remains using short-amplicon marker analysis of severely degraded DNA extracted from a decomposed and charred femur
    • M. Fondevila, C. Phillips, N. Naveran, L. Fernandez, M. Cerezo, A. Salas, A. Carrecedo, M.V. Lareu, 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. 2 (2008) 212-218.
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    • Fondevila, M.1    Phillips, C.2    Naveran, N.3    Fernandez, L.4    Cerezo, M.5    Salas, A.6    Carrecedo, A.7    Lareu, M.V.8
  • 18
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    • Scientific standards for studies in forensic genetics
    • P.M. Schneider, Scientific standards for studies in forensic genetics, Forensic Sci. Int. 165 (2007) 238-243.
    • (2007) Forensic Sci. Int. , vol.165 , pp. 238-243
    • Schneider, P.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.