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

Author:

Lee Hyo-Jung,Lee Jae Won,Jeong Su Jin,Park Mira

Funder

Ministry of Science, ICT and Future Planning (KR)

Prosecutors’ Office, Republic of Korea

Publisher

Springer Science and Business Media LLC

Subject

Pathology and Forensic Medicine

Reference19 articles.

1. Brinkmann B, Klintschar M, Neuhuber F, Huhne J, Rolf B (1998) Mutation rate in human microsatellites: influence of the structure and length of the tandem repeat. Am J Hum Genet 62:1408–1415

2. Nachman MW, Crowell SL (2000) Estimate of the mutation rate per nucleotide in humans. Genetics 156:297–304

3. Kondrashow AS (2003) Direct estimates of human per nucleotide mutation rates at 20 loci causing Mendelian diseases. Hum Mutat 21:12–27

4. Amorim A, Pereira L (2005) Pros and cons in the use of SNPs in forensic kinship investigation: a comparative analysis with STRs. Forensic Sci Int 150:17–21

5. Lisa DW, John MS, Jeffrey JT, Rick WS (1998) Human identification by genotyping single nucleotide polymorphisms (SNPs) using an APEX microarray. Genetic Identity Conference Proceedings, Ninth International Symposium on Human Identification

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