Application of a dense SNP PCR multiplex for high throughput kinship determination using Next Generation Sequencing (NGS)
Author:
Publisher
Elsevier BV
Subject
Genetics,Pathology and Forensic Medicine
Reference7 articles.
1. Identification of missing persons through kinship analysis by microhaplotype sequencing of single-source DNA and two-person DNA mixtures;Bai;Forensic Sci. Int. Genet.,2022
2. Assessment of impact of DNA extraction methods on analysis of human remain samples on massively parallel sequencing success;Zeng;Int. J. Leg. Med.,2019
3. Large scale DNA identification: the ICMP experience;Parsons;Forensic Sci. Int. Genet.,2019
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1. Comparison of next generation sequencing (NGS) - (SNPs) and capillary electrophoresis (CE) - (STRs) in the genetic analysis of human remains;Forensic Science International: Genetics;2025-01
2. Developmental validation of the ForenSeq® Kintelligence kit, MiSeq FGx® sequencing system and ForenSeq Universal Analysis Software;Forensic Science International: Genetics;2024-07
3. Operationalisation of the ForenSeq® Kintelligence Kit for Australian unidentified and missing persons casework;Forensic Science International: Genetics;2024-01
4. A cost–benefit analysis for use of large SNP panels and high throughput typing for forensic investigative genetic genealogy;International Journal of Legal Medicine;2023-06-21
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