In forensics, weight is assigned to the results

of an mtDNA match comparison by estimating the frequency of the mtDNA haplotype given a relevant population sample. While concerted efforts have been put forth in recent years to establish high-quality Everolimus nmr mtDNA control region reference datasets representing U.S. and global population groups [21], [22] and [23], similar initiatives targeting the mtDNA coding region have been lacking. Although more than 20,000 complete human mtGenome sequences have now been published (see the PhyloTree website http://www.phylotree.org/mtDNA_seqs.htm[24] for a comprehensive list of publications as of 19 February 2014), none have been developed as U.S.-wide population reference data that meet current forensic standards [20], [25] and [26]. To meet the NVP-BGJ398 research buy need for forensic-quality population reference data for the full mtGenome, we report here 588 mtGenome haplotypes from three U.S. populations (African American, U.S. Caucasian and U.S. Hispanic). These Sanger-based data were developed in accordance with current best practices for mtDNA data generation [25] and [26] to ensure their suitability for forensic use. In this paper we report summary statistics for the complete mtGenome and evaluate the statistical weight of a previously unobserved haplotype, and we

compare the composition of each population sample to previously published CR-based datasets to establish their consistency and representativeness. In addition, we examine the coding region insertion/deletion polymorphisms (indels) and the heteroplasmies detected in the haplotypes in detail to help inform future analyses and use of complete mtGenome data for forensic and other purposes. The samples used for this databasing initiative were anonymized blood serum specimens from the Department of Defense Serum Repository (DoDSR; [27]). The 175 African-American, 275 U.S. Caucasian,

and 175 U.S. Hispanic samples initially targeted for processing were selected randomly from specimens Glutathione peroxidase in the DoDSR collection. Specimens were received with only state and self-reported population/ethnicity information. This research involving human subjects, human material or human data was reviewed by the U.S. Army Medical Research and Materiel Command’s Office of Research Protections, Institutional Review Board Office, and was granted an exemption from requiring ethics approval. Full mtGenome haplotypes were generated from the blood serum specimens using the protocol and high-throughput processing strategy described in Lyons et al. [28], with the minor modifications described in Just et al. [29]. In brief: Blood serum specimens were robotically transferred from tubes to 96-well plates. Genomic DNA was extracted from 100 μl of blood serum using the QIAamp 96 DNA Blood Kit (QIAGEN, Valencia, CA), and a combination of robotic pipetting and manual centrifugation.