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Correction: Shelly Y. Shih; et al.; Applications of Probe Capture Enrichment Next Generation Sequencing for Whole Mitochondrial Genome and 426 Nuclear SNPs for Forensically Challenging Samples. Genes 2018, 9, 49

NCJ Number
310015
Journal
Genes Volume: 9 Issue: 2 Dated: February 2018 Pages: 1-2
Author(s)
Shelly Y. Shih; Nikhil Bose; Anna Beatriz R. Gonçalves; Henry A. Erlich; Cassandra D. Calloway
Date Published
February 2018
Length
2 pages
Annotation

This article makes corrections to a previously published article that demonstrated the use of target enrichment through probe capture rather than PCR amplification, for the analysis of limited and mock degraded samples using the authors’ custom probe capture panels for massively parallel sequencing of the whole mtgenome and 426 SNP markers; and it notes that results obtained on individual telogen hairs demonstrate the potential of probe capture NGS analysis for mtDNA and nuclear SNPs for challenging forensic specimens.

Abstract

The authors wish to make the following change to their paper [1]. Four new references were added: [55] “55. SeqPrep. Available online: https://github.com/jstjohn/SeqPrep (accessed on 13 November 2017)”, [57] “57. Burrow Burrow-Wheeler Aligner. Available online: https://github.com/lh3/bwa (accessed on 13 November 2017)”, [58] “58. SAMTools. Available online: https://github.com/samtools/samtools (accessed on 13 November 2017)” and [59] “59. EMPOP. Available online: https://empop.online/ (accessed on 10 November 2017).” These references are added in Section 2.4., fourth paragraph, and the text now reads: “In addition to GeneMarker®HTS, the sequenced reads for the mtDNA mixture samples were analyzed using Mixemt, developed by Vohr et al. [54]. Prior to analysis using Mixemt, the raw sequence reads were trimmed for adapters, and the overlapping reads were merged using SeqPrep [55]. Both merged and unmerged sequence reads were then aligned separately to the Reconstructed Sapiens Reference Sequence (RSRS) using the Burrows–Wheeler Aligner (bwa) tool, which also converts the FASTQ files to SAM files [56,57]. SAMtools was then used to collapse the PCR duplicates and convert SAM files to BAM files [58]. The BAM files were used for Mixemt analysis, which assigns each sequence read to a haplogroup based on the probability of the read originating from a contributing haplogroup [50,54].” Due to this change, the references in the Discussion are renumbered: reference [57] is now [60], reference [58] is now [61], reference [59] is now [62] , reference [60] is now [63] , reference [61] is now [64] , reference [62] is now [65] , reference [63] is now [66] , reference [64] is now [67] and reference [65] is now [68]. The authors apologize for any inconvenience caused to the readers by this omission. The manuscript will be updated and the original will remain online on the article webpage. (Published Abstract Provided)