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Selecting Microhaplotypes Optimized for Different Purposes

NCJ Number
254331
Date Published
2018
Length
9 pages
Author(s)
Kenneth K. Kidd; Andrew J. Pakstis; William C. Speed; Robert Lagare; Sharon Wootton; Joseph Chang
Agencies
NIJ-Sponsored
Publication Type
Research (Applied/Empirical), Report (Study/Research), Report (Grant Sponsored), Program/Project Description
Grant Number(s)
2013-DN-BX- K023, 2015-DN-BX-K023, 2014-DN-BX-K030
Annotation
This article reports on a project that has conducted various DNA analyses for 83 populations in an ongoing study for a subset of the best microhaplotypes currently available, illustrating their characteristics and potential utility for ancestry, identification, and mixture deconvolution.
Abstract
Massively parallel sequencing is transforming forensic work by allowing various useful forensic markers, such as STRPs and SNPs, to be multiplexed, providing information on ancestry, individual and familial identification, phenotypes for eye/hair/skin pigmentation, and the deconvolution of mixtures. Microhaplotypes also become feasible with massively parallel sequencing. These are DNA segments (smaller than 300 nucleotides) that are selected to contain multiple SNPs unambiguously defining three or more haplotype alleles occurring at common frequencies. The physical extent of a microhaplotype can thus be covered by a single sequence read, making these loci phase-known codominant genetic systems. Such microhaplotypes supply significantly more information than a single SNP. The project's efforts to develop useful sets of microhaplotypes have already identified 182 such loci that the project has studied on a large number of human populations from around the world. (publisher abstract modified)
Date Created: July 20, 2021