Forensic Science International: Genetics
Volume 6, Issue 3 , Pages 354-365, May 2012

The recombination landscape around forensic STRs: Accurate measurement of genetic distances between syntenic STR pairs using HapMap high density SNP data

  • C. Phillips

      Affiliations

    • Forensic Genetics Unit, Institute of Legal Medicine, University of Santiago de Compostela, Spain
    • Corresponding Author InformationCorresponding author.
  • ,
  • D. Ballard

      Affiliations

    • Academic Haematology Unit, Pathology Group, Blizard Institute, Barts and the London, Queen Mary's School of Medicine & Dentistry, London, UK
  • ,
  • P. Gill

      Affiliations

    • Institute of Forensic Medicine, Rikshospitalet, University of Oslo, Norway
  • ,
  • D. Syndercombe Court

      Affiliations

    • Academic Haematology Unit, Pathology Group, Blizard Institute, Barts and the London, Queen Mary's School of Medicine & Dentistry, London, UK
  • ,
  • Á. Carracedo

      Affiliations

    • Forensic Genetics Unit, Institute of Legal Medicine, University of Santiago de Compostela, Spain
  • ,
  • M.V. Lareu

      Affiliations

    • Forensic Genetics Unit, Institute of Legal Medicine, University of Santiago de Compostela, Spain

Received 6 June 2011; received in revised form 9 July 2011; accepted 24 July 2011. published online 29 August 2011.

Abstract 

Family studies can be used to measure the genetic distance between same-chromosome (syntenic) STRs in order to detect physical linkage or linkage disequilibrium. However, family studies are expensive and time consuming, in many cases uninformative, and lack a reliable means to infer the phase of the diplotypes obtained. HapMap provides a more comprehensive and fine-scale estimation of recombination rates using high density multi-point SNP data (average inter-SNP distance: 900 nucleotides). Data at this fine scale detects sub-kilobase genetic distances across the whole recombining human genome. We have used the most recent HapMap SNP data release 22 to measure and compare genetic distances, and by inference fine-scale recombination rates, between 29 syntenic STR pairs identified from 39 validated STRs currently available for forensic use. The 39 STRs comprise 23 core loci: SE33, Penta D & E, 13 CODIS and 7 non-CODIS European Standard Set STRs, plus supplementary STRs in the recently released Promega CS-7™ and Qiagen Investigator HDplex™ kits. Also included were D9S1120, a marker we developed for forensic use unique to chromosome 9, and the novel D6S1043 component STR of SinoFiler™ (Applied Biosystems). The data collated provides reliable estimates of recombination rates between each STR pair, that can then be placed into haplotype frequency calculators for short pedigrees with multiple meiotic inputs and which just requires the addition of allele frequencies. This allows all current STR sets or their combinations to be used in supplemented paternity analyses without the need for further adjustment for physical linkage. The detailed analysis of recombination rates made for autosomal forensic STRs was extended to the more than 50 X chromosome STRs established or in development for complex kinship analyses.

Keywords: Linkage, Linkage disequilibrium, STRs, X-STRs, Recombination, Genetic distance, Genetic maps

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PII: S1872-4973(11)00147-5

doi:10.1016/j.fsigen.2011.07.012

Forensic Science International: Genetics
Volume 6, Issue 3 , Pages 354-365, May 2012