Literature DB >> 28243773

How many single nucleotide polymorphisms (SNPs) are needed to replace short tandem repeats (STRs) in forensic applications?

Hyo-Jung Lee1, Jae Won Lee2, Su Jin Jeong2, Mira Park3.   

Abstract

Short tandem repeats (STRs) are the most commonly used forms of genetic information in forensic identification. In recent times, advances in the information on single nucleotide polymorphisms (SNPs) have raised the possibility that these markers could replace the forensically established STRs. In this work, we conducted comparative simulation studies that allowed us to estimate the number of SNPs needed if these markers were used instead of STRs in criminal cases and paternity investigations.

Keywords:  Short tandem repeats; Single nucleotide polymorphisms

Mesh:

Year:  2017        PMID: 28243773     DOI: 10.1007/s00414-017-1564-z

Source DB:  PubMed          Journal:  Int J Legal Med        ISSN: 0937-9827            Impact factor:   2.686


  15 in total

1.  Evaluation of DNA match probability in criminal case.

Authors:  J W Lee; H S Lee; M Park; J J Hwang
Journal:  Forensic Sci Int       Date:  2001-02-15       Impact factor: 2.395

2.  Motherless case in paternity testing.

Authors:  H S Lee; J W Lee; G R Han; J J Hwang
Journal:  Forensic Sci Int       Date:  2000-11-13       Impact factor: 2.395

3.  Estimate of the mutation rate per nucleotide in humans.

Authors:  M W Nachman; S L Crowell
Journal:  Genetics       Date:  2000-09       Impact factor: 4.562

4.  Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat.

Authors:  B Brinkmann; M Klintschar; F Neuhuber; J Hühne; B Rolf
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

5.  Development of SNP-based human identification system.

Authors:  Jae-Jung Kim; Bok-Ghee Han; Hae-In Lee; Han-Wook Yoo; Jong-Keuk Lee
Journal:  Int J Legal Med       Date:  2010-03       Impact factor: 2.686

6.  Interpreting forensic DNA evidence on the basis of hypotheses testing.

Authors:  N Fukshansky; W Bär
Journal:  Int J Legal Med       Date:  1998       Impact factor: 2.686

Review 7.  Interpreting DNA mixtures.

Authors:  B S Weir; C M Triggs; L Starling; L I Stowell; K A Walsh; J Buckleton
Journal:  J Forensic Sci       Date:  1997-03       Impact factor: 1.832

8.  Genetic variation of 23 autosomal STR loci in Korean population.

Authors:  Jung-Hyun Park; Seung-Bum Hong; Ji-Young Kim; Yosep Chong; Sinae Han; Chung-Hyun Jeon; Hee-Jung Ahn
Journal:  Forensic Sci Int Genet       Date:  2013-01-18       Impact factor: 4.882

9.  Blood samples: probability of discrimination.

Authors:  D A Jones
Journal:  J Forensic Sci Soc       Date:  1972-04

10.  Direct estimates of human per nucleotide mutation rates at 20 loci causing Mendelian diseases.

Authors:  Alexey S Kondrashov
Journal:  Hum Mutat       Date:  2003-01       Impact factor: 4.878

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  2 in total

1.  A SNP panel for early detection of artificial chimerism in HSCT patients using TaqMan technology.

Authors:  Tikumphorn Sathirapatya; Wikanda Worrapitirungsi; Poonyapat Sukawutthiya; Kawin Rasmeepaisarn; Kornkiat Vongpaisarnsin
Journal:  Int J Legal Med       Date:  2020-04-05       Impact factor: 2.686

2.  A SNP panel and online tool for checking genotype concordance through comparing QR codes.

Authors:  Yonghong Du; Joshua S Martin; John McGee; Yuchen Yang; Eric Yi Liu; Yingrui Sun; Matthias Geihs; Xuejun Kong; Eric Lingfeng Zhou; Yun Li; Jie Huang
Journal:  PLoS One       Date:  2017-09-19       Impact factor: 3.240

  2 in total

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