Abstract

Massively parallel sequencing following hybridisation enrichment provides new opportunities to obtain genetic data for various types of forensic testing and has proven successful on modern as well as degraded and ancient DNA. A customisable forensic intelligence panel that targeted 124 SNP markers (67 ancestry informative markers, 23 phenotype markers from the HIrisplex panel, and 35 Y-chromosome SNPs) was used to examine biogeographic ancestry, phenotype and sex and Y-lineage in samples from different ethnic populations of Pakistan including Pothwari, Gilgit, Baloach, Pathan, Kashmiri and Siraiki. Targeted sequencing and computational data analysis pipeline allowed filtering of variants across the targeted loci. Study samples showed an admixture between East Asian and European ancestry. Eye colour was predicted accurately based on the highest p-value giving overall prediction accuracy of 92.8%. Predictions were consistent with reported hair colour for all samples, using the combined highest p-value approach and step-wise model incorporating probability thresholds for light or dark shade. Y-SNPs were successfully recovered only from male samples which indicates the ability of this method to identify biological sex and allow inference of Y-haplogroup. Our results demonstrate practicality of using hybridisation enrichment and MPS to aid in human intelligence gathering and will open many insights into forensic research in South Asia.

Highlights

  • DNA was successfully extracted from the samples and after fragmentation, DNA libraries were constructed for each sample prior to hybridisation enrichment and massively parallel sequencing (MPS)

  • In an attempt to analyze various marker types together in one analytical workflow for forensic human intelligence information, a novel customisable hybridisation enrichment forensic intelligence panel has been used in the present research which provided new avenues and opened many insights to forensic human identification

  • This panel facilitates a technical approach that permits the possibility of using customisable single nucleotide polymorphisms (SNPs) marker sets relevant to the question under study for hybridisation enrichment prior to MPS

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Summary

Introduction

SNPs are more stable genetic markers in most of the sensitive situations such as ancestry cases like inheritance/kinship, provides investigative lead value in cases having no genetic profile match in DNA databases or with no suspect, and in family reconstructions in case of missing individuals and unknown human remains (where the DNA is significantly fragmented). This is because of the fact that they have comparatively low mutation rates [3]. SNP variation in pigmentation genes can be useful for inferring visible phenotypic traits for example hair, skin and eye colour [4]

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