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复合扩增9个STR位点在亲子鉴定中的应用评估 被引量:12

Evaluation of 9 STR Loci in paternity identification
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摘要 在法医学亲子鉴定中应用复合扩增及四色荧光自动分析技术检测 Profiler plusTM9个 STR位点,一次性获得的信息量大,累计非父排除率达 0.9999。应用于 268例亲子鉴定的结果表明, 9个具有高度多态性 STR基因座的联合检测,能使三联体亲子鉴定的排除结论明确无误。对不排除案例,其 RCP值均可达国际认定标准。对二联体亲子鉴定一般需增加 CofilerTM试剂盒 4个 STR位点检测。 9 STR loci obtained by four- dye fluorescent labeling technique in paternity identification provides much information at one test and the cumulative chance of exclusion gets up to 0.9999. Our result of 268 paternity test cases shows that there are at least two incompatible loci in all Mother- Child- Alleged Father (M- C- AF) exclusive cases. To those unexclusive cases, The RCP all reaches international standard. It is suggested that more STR loci be used for accurate test in Child- Alleged Father(C- AF) case.
出处 《法医学杂志》 CAS CSCD 2000年第4期216-218,共3页 Journal of Forensic Medicine
基金 国家计委立项课题!(国家计委 财政部 [1998]计高技 2444号)
关键词 亲子鉴定 STR位点 突变 非父排除率 paternity identification, STR loci, mutation, paternity exclusive, paternity index
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  • 1Bar w,Brinkmann B,Budowle B,et al.DNA recommendations: Further report of the DNACommossion of the ISFH regarding the use of short tandem repeat systems[J].Int J LegaMed,1997,110:175- 176.
  • 2Dib C,Faure S,Fizames C.A comprehensive genetic map of the human genome based on5,264 microsatellites[J].Nature,1996,380:152- 154.
  • 3Gill P, Ivanov PL, Kimpton C. Identification of the remains of the Romanov familyby DNA analysis[J].Nat Genet, 1994,6:130- 135.
  • 4Roy MS, Girman DJ, Taylor AC. The use of museum specimens to reconstruct thegenetic variability and relationships of extinct populations[J].Experientia,1994,50(6):551-557.
  • 5Poinar GO Jr. The range of life in amber: singificance and implications in DNAstudies[J]. Experientia, 1994,50(6):536- 42.
  • 6Tuross N.The biochemistry of ancient DNA in bone[J]. Experientia,1994,50(6):530- 5.
  • 7Weir BS.DNA statistics in the Simpson matter[J].Nat Genet, 1995,11:365-368.
  • 8Hou Y,Mulcahy- Schroeder M,Mielke M,et al.Genetic variation at the short tandemrepeat loci HUMTH01 and HUMVWA within and between Chinese and German populations[J].MedizinischeGenetik, 1996,8(1):101.
  • 9Hou Y,Walter H.Genetic substructure at the STR loci HUMTH01 and HUMVWA in Hanpopulations, China[A]. Carracedo A, Brinkmann B, Baer W. Advance in ForensicHaemogenetics 6[M].Springer- Verlag:Berlin Heidelberg New York,1996:468- 470.
  • 10Moller A, Meyer E, Brinkmann B. Different types of structural variation in STR:HumFES/FPS,HumVWA and D21S11[J].Int J Leg Med,1994,106:319- 323.

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