GillP. Role of short tandem repeat DNA in forensic casework in the UK—past, present, and future perspectives. Biotechniques, 2002; 32:366–368, 370, 372, passim.
2.
HuangQY, XuFH, ShenH, et al.Mutation patterns at dinucleotide microsatellite loci in humans. Am J Hum Genet, 2002; 70:625–634.
3.
ReichDE, SchaffnerSF, DalyMJ, et al.Human genome sequence variation and the influence of gene history, mutation and recombination. Nat Genet, 2002; 32:135–142.
4.
KimJJ, HanBG, LeeH, et al.Development of SNP-based human identification system. Int J Legal Med, 2010; 124:125–131.
5.
LeeHY, ParkMJ, YooJE, et al.Selection of twenty-four highly informative SNP markers for human identification and paternity analysis in Koreans. Forensic Sci Int, 2005; 148:107–112.
6.
ChoS, YuHJ, HanJ, et al.Forensic application of SNP-based resequencing array for individual identification. Forensic Sci Int Genet, 2014; 13:45–52.
JonesDA: Blood samples: Probability of discrimination. J Forensic Sci Soc, 1972; 12:355–359.
9.
JunG, FlickingerM, HetrickKN, et al.Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data. Am J Hum Genet, 2012; 91:839–848.
