Insertion-deletion polymorphisms--utilization on forensic analysis

Int J Legal Med. 2012 Jul;126(4):491-6. doi: 10.1007/s00414-011-0588-z. Epub 2011 Jun 7.

Abstract

Insertion-deletion (INDEL) markers are very frequent in the human genome and present several advantages for population and forensic studies, such as low mutation rates, easy interpretation, small amplicons, easy genotyping, and the possibility of using multiplex PCR. The great adaptability of INDELs for amplification of low copy number or degraded DNA allows its using as an interesting platform of genetic identity by DNA in forensic cases. In the present study, we tested the ability of 48 diallelic INDEL markers on genotyping forensic samples collected from different biological samples related to criminal cases. Moreover, we evaluated the lowest DNA concentration with which there was amplification of all markers from each one of three indel-plex panels. When comparing the performances obtained by the indel-plex panels described in this study with results obtained using Identifiler® kit (Applied Biosystems) related to forensic samples, as well as to control samples with different concentrations of DNA, we observed superior efficiency on samples with low copy number or in the presence of inhibitors.

MeSH terms

  • DNA / analysis
  • DNA Fingerprinting / methods*
  • Electrophoresis
  • Female
  • Genome, Human
  • Genotype
  • Humans
  • INDEL Mutation*
  • Male
  • Microsatellite Repeats
  • Polymerase Chain Reaction
  • Polymorphism, Single Nucleotide*
  • Racial Groups / genetics

Substances

  • DNA