Evaluation of the Microhaplotypes panel for DNA mixture analyses

Forensic Sci Int Genet. 2018 Jul:35:149-155. doi: 10.1016/j.fsigen.2018.05.003. Epub 2018 May 12.

Abstract

The identification of a suspect in a DNA mixture typed with the standard short tandem repeat polymorphism (STR) kits has faced challenges. Several improved methods or technologies have been introduced to address this issue. However, some complex situations in the process remain elusive. In the present study, we presented a panel of 26 tiny microhaplotypes, each generating a relatively high (>3.0) effective number of alleles (Ae) and possessing low (<50 bp) sequence lengths. The average Ae and heterozygosity values among the 9 populations of 26 microhaps were in ranges from 2.60 to 4.54 and 0.59 to 0.96, respectively. Power of discrimination and power of exclusion values were ranged from 0.49 to 0.87 and 0.29 to 0.94, respectively. Significant positive correlations have been found between Ae values and heterozygosity (r = 0.43, p = 0.02) or power of discrimination values (r = 0.55, p = 0.003), respectively. The cumulative probability of detecting a mixture of two unrelated individuals could reach 0.9999998 when using a panel of 26 microhaps with Ae = 3. We further tested the panel by using massively parallel sequencing, and 14 out of 26 microhaps were successfully genotyped in a single multiplex system. 60 unrelated Chinese Han individuals and 2 artificially prepared samples mixed by two unrelated contributors (in duplicate, ie. 4 mixtures) were sequenced. Approximately 32.14% of the 14 loci presented three or four alleles in the two mixtures. The likelihood ratio values to cognizance the mixtures' contributor were in a range from 1.95 × 106 to 1.10 × 107. The results demonstrated that the present panel could offer a valuable complementary tool in forensic applications.

Keywords: Effective number of alleles, A(e); Likelihood ratio; Microhaplotype; Mixture.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA / genetics*
  • DNA Fingerprinting
  • Ethnicity / genetics
  • Haplotypes*
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Likelihood Functions
  • Polymerase Chain Reaction
  • Polymorphism, Single Nucleotide*
  • Racial Groups / genetics
  • Sequence Analysis, DNA

Substances

  • DNA