Construction and forensic genetic characterization of 11 autosomal haplotypes consisting of 22 tri-allelic indels

Forensic Sci Int Genet. 2018 May:34:71-80. doi: 10.1016/j.fsigen.2018.02.001. Epub 2018 Feb 6.

Abstract

Insertion/deletion polymorphisms (indels), which combine the advantages of both short tandem repeats and single-nucleotide polymorphisms, are suitable for parentage testing. To overcome the limitations of the low polymorphism of di-allelic indels, we constructed a set of haplotypes with physically linked, multi-allelic indels. Candidate haplotypes were selected from the 1000 Genomes Project database, and were subject to the following criteria for inclusion: (i) each marker must have a minimum allele frequency (MAF) of ≥0.1 in the Han population of China; (ii) markers must exist in a non-coding region; (iii) the physical distance between a pair of candidate indels must be <500 bp; (iv) the allele length variation of each indel from 1 to 20 bp; (v) different haplotypes must be located on different chromosomes or chromosomal arms, or be more than 10 Mb apart if on the same chromosomal arm; and (vi) they must not be located across a recombination hotspot. A multiplex system with 11 haplotype markers, comprising 22 tri-allelic indel loci distributed over 10 chromosomes was developed. To validate the multiplex panel, we investigated the haplotype distribution in sets of two and three-generation pedigrees. The results demonstrated that the haplotypes consisting of multi-allelic indel markers exhibited higher polymorphism than a single indel locus, and thus provide Supplementary information for forensic kinship identification.

Keywords: Forensic genetics; Haplotype; Indels; Tri-allelic.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Electrophoresis, Capillary
  • Forensic Genetics / methods*
  • Gene Frequency
  • Genotype
  • Haplotypes*
  • Humans
  • INDEL Mutation*
  • Polymerase Chain Reaction