Targeted enrichment of whole‐genome SNPs from highly burned skeletal remains

单核苷酸多态性 计算生物学 生物 基因组 遗传学 基因 基因型
作者
Matthew V. Emery,Katelyn L. Bolhofner,Laure Spake,Suhail Ghafoor,Cyril J Versoza,Erin Rawls,Stevie Winingear,Jane E. Buikstra,Odile Loreille,Laura C. Fulginiti,Anne C. Stone
出处
期刊:Journal of Forensic Sciences [Wiley]
标识
DOI:10.1111/1556-4029.15482
摘要

Abstract Genetic assessment of highly incinerated and/or degraded human skeletal material is a persistent challenge in forensic DNA analysis, including identifying victims of mass disasters. Few studies have investigated the impact of thermal degradation on whole‐genome single‐nucleotide polymorphism (SNP) quality and quantity using next‐generation sequencing (NGS). We present whole‐genome SNP data obtained from the bones and teeth of 27 fire victims using two DNA extraction techniques. Extracts were converted to double‐stranded DNA libraries then enriched for whole‐genome SNPs using unpublished biotinylated RNA baits and sequenced on an Illumina NextSeq 550 platform. Raw reads were processed using the EAGER (Efficient Ancient Genome Reconstruction) pipeline, and the SNPs filtered and called using FreeBayes and GATK (v. 3.8). Mixed‐effects modeling of the data suggest that SNP variability and preservation is predominantly determined by skeletal element and burn category, and not by extraction type. Whole‐genome SNP data suggest that selecting long bones, hand and foot bones, and teeth subjected to temperatures <350°C are the most likely sources for higher genomic DNA yields. Furthermore, we observed an inverse correlation between the number of captured SNPs and the extent to which samples were burned, as well as a significant decrease in the total number of SNPs measured for samples subjected to temperatures >350°C. Our data complement previous analyses of burned human remains that compare extraction methods for downstream forensic applications and support the idea of adopting a modified Dabney extraction technique when traditional forensic methods fail to produce DNA yields sufficient for genetic identification.
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