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Application of a custom haplotype caller to analyze sequence-based data of 56 microhaplotypes.
Kwon, Ye-Lim; Lee, Eun Young; Kim, Bo Min; Joo, Su Min; Jeong, Kyu Sik; Chun, Byung Won; Lee, Yang Han; Park, Ki Won; Shin, Kyoung-Jin.
Afiliação
  • Kwon YL; Department of Forensic Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University, Seoul 03722, Republic of Korea. Electronic address: yelim117@yuhs.ac.
  • Lee EY; Department of Forensic Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea. Electronic address: -silver02-@hanmail.net.
  • Kim BM; Department of Forensic Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University, Seoul 03722, Republic of Korea. Electronic address: kbomin526@snu.ac.kr.
  • Joo SM; Department of Forensic Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University, Seoul 03722, Republic of Korea. Electronic address: juicemin@yuhs.ac.
  • Jeong KS; Forensic DNA division, National Forensic Service, Wonju-si, Gangwon-do 26460, Republic of Korea. Electronic address: ks0703@korea.kr.
  • Chun BW; DNA analysis Division, National Forensic Service Daejeon Institute, Daejeon 34054, Republic of Korea. Electronic address: warney@korea.kr.
  • Lee YH; Forensic DNA division, National Forensic Service, Wonju-si, Gangwon-do 26460, Republic of Korea. Electronic address: nisi7118@naver.com.
  • Park KW; Forensic DNA division, National Forensic Service, Wonju-si, Gangwon-do 26460, Republic of Korea. Electronic address: kwpark001@hanmail.net.
  • Shin KJ; Department of Forensic Medicine, Yonsei University College of Medicine, Seoul 03722, Republic of Korea; Graduate School of Medical Science, Brain Korea 21 Project, Yonsei University, Seoul 03722, Republic of Korea. Electronic address: KJSHIN@yuhs.ac.
Forensic Sci Int Genet ; 61: 102778, 2022 11.
Article em En | MEDLINE | ID: mdl-36166997
ABSTRACT
Microhaplotypes (microhaps) are recently introduced markers that aim to complement the limitations of conventional forensic markers such as short tandem repeats (STRs) and single nucleotide polymorphisms (SNPs). With the potential of microhaps in forensics becoming clearer through massively parallel sequencing (MPS), MPS-based studies on microhaps are being actively reported. However, simpler workflow schemes for the generation and analysis of MPS data are still required to facilitate the practical application of MPS in forensics. In this study, we developed an in-house MPS panel that simultaneously amplifies 56 microhaps and a custom haplotype caller, Visual Microhap. The developed tool works on a web browser and provides four analysis options to extract SNP-based haplotypes from sequence-based data obtained by STRait Razor 3.0. To demonstrate the utility of the MPS panel and data analysis workflow scheme, we also analyzed 56 microhaps of 286 samples from four populations (African-American, Caucasian, Hispanic, and Korean). The average effective number of alleles (Ae) for the four groups was 3.45, ranging from 1.74 to 6.98. Forensic statistical parameters showed that this microhap panel is more powerful than conventional autosomal STRs for human identification. Meanwhile, the 56-plex panel mostly comprised microhaps with high Ae; however, the four populations were grossly distinguishable from each other by cluster analysis. Consequently, the developed in-house MPS panel for 56 microhaps and the adopted workflow using open-source tools can increase the utility of microhap MPS in forensic research and practice.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Impressões Digitais de DNA / Sequenciamento de Nucleotídeos em Larga Escala Limite: Humans Idioma: En Revista: Forensic Sci Int Genet Assunto da revista: GENETICA / JURISPRUDENCIA Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Impressões Digitais de DNA / Sequenciamento de Nucleotídeos em Larga Escala Limite: Humans Idioma: En Revista: Forensic Sci Int Genet Assunto da revista: GENETICA / JURISPRUDENCIA Ano de publicação: 2022 Tipo de documento: Article