Application of Restriction Landmark Genomic Scanning (RLGS) to paternity tests and personal identification
被引:0
|
作者:
Sawaguchi, Toshiko
论文数: 0引用数: 0
h-index: 0
机构:
Tokyo Womens Med Univ, Sch Med, Dept Legal Med, Shinjuku Ku, Tokyo 1628666, JapanTokyo Womens Med Univ, Sch Med, Dept Legal Med, Shinjuku Ku, Tokyo 1628666, Japan
Sawaguchi, Toshiko
[1
]
Takashi, Taki
论文数: 0引用数: 0
h-index: 0
机构:
Tokyo Womens Med Univ, Sch Med, Dept Legal Med, Shinjuku Ku, Tokyo 1628666, JapanTokyo Womens Med Univ, Sch Med, Dept Legal Med, Shinjuku Ku, Tokyo 1628666, Japan
Takashi, Taki
[1
]
Hasegawa, Chica
论文数: 0引用数: 0
h-index: 0
机构:
Tokyo Womens Med Univ, Sch Med, Dept Legal Med, Shinjuku Ku, Tokyo 1628666, JapanTokyo Womens Med Univ, Sch Med, Dept Legal Med, Shinjuku Ku, Tokyo 1628666, Japan
Hasegawa, Chica
[1
]
机构:
[1] Tokyo Womens Med Univ, Sch Med, Dept Legal Med, Shinjuku Ku, Tokyo 1628666, Japan
来源:
INTERNATIONAL MEDICAL JOURNAL
|
2007年
/
14卷
/
03期
关键词:
Restriction Landmark Genomic Scanning (RLGS);
forensic medicine;
personal identification;
paternity test;
Postmortem Time Interval (PMI);
D O I:
暂无
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Materials & Methods: RLGS method was carried out using genomic DNA from the following samples; (1) blood samples from 2 unrelated Japanese, (2) blood samples from 3 familial Japanese (3) blood samples from a Japanese, after 0 hour, 3 days and 5 days postmortem at 4 degrees C Objective: Restriction landmark genomic scanning (RLGS) has been developed in Japan to scan genomes with the highest degree of accuracy possible. The RLGS method employs direct-end labeling of a genome digested by restriction enzymes and then subjected to high-resolution two-dimensional electrophoresis. The purpose of this report is to investigate the possibility of forensic application of RLGS. Result: As a result of its application in paternity tests and personal identification, common spots was recognized in the electrophoresis from Japanese familial samples and identified. The dependent specific spots were recognized from the two unrelated Japanese. The coincidental rate of common spots in Japanese familial samples was higher (97%) than those in unrelated personal samples (92%). As a result of the application in analysis of the postmortem interval, the number of spots was shown not to depend on the time interval after blood sampling. Conclusion: This study proposes the application of RLGS to paternity tests and forensic personal identification and the necessity of modification of RLGS to the analysis of postmortem time phenomenon.
机构:
NCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USANCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
Wang, Sophia S.
Smiraglia, Dominic J.
论文数: 0引用数: 0
h-index: 0
机构:
Roswell Pk Canc Inst, Dept Canc Genet, Buffalo, NY 14263 USANCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
Smiraglia, Dominic J.
Wu, Yue-Zhong
论文数: 0引用数: 0
h-index: 0
机构:
Ohio State Univ, Div Human Canc Genet, Columbus, OH 43210 USANCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
Wu, Yue-Zhong
Ghosh, Srimoyee
论文数: 0引用数: 0
h-index: 0
机构:
Roswell Pk Canc Inst, Dept Canc Genet, Buffalo, NY 14263 USANCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
Ghosh, Srimoyee
Rader, Janet S.
论文数: 0引用数: 0
h-index: 0
机构:
Washington Univ, Sch Med, Dept Obstet & Gynecol, St Louis, MO 63110 USANCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
Rader, Janet S.
Cho, Kathleen R.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI USA
Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI USANCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
Cho, Kathleen R.
Bonfiglio, Thomas A.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Rochester, Sch Med, Dept Pathol & Lab Med, Rochester, NY USANCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
Bonfiglio, Thomas A.
Nayar, Ritu
论文数: 0引用数: 0
h-index: 0
机构:
Northwestern Univ, Dept Pathol, Feinberg Sch Med, Chicago, IL 60611 USANCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
Nayar, Ritu
Plass, Christoph
论文数: 0引用数: 0
h-index: 0
机构:
Ohio State Univ, Div Human Canc Genet, Columbus, OH 43210 USANCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
Plass, Christoph
Sherman, Mark E.
论文数: 0引用数: 0
h-index: 0
机构:
NCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USANCI, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA