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      Law enforcement use of genetic genealogy databases in criminal investigations: Nomenclature, definition and scope

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          Abstract

          Although law enforcement use of commercial genetic genealogy databases has gained prominence since the arrest of the Golden State Killer in 2018, and it has been used in hundreds of cases in the United States and more recently in Europe and Australia, it does not have a standard nomenclature and scope. We analyzed the more common terms currently being used and propose a common nomenclature: investigative forensic genetic genealogy (iFGG). We define iFGG as the use by law enforcement of genetic genealogy combined with traditional genealogy to generate suspect investigational leads from forensic samples in criminal investigations. We describe iFGG as a proper subset of forensic genetic genealogy, that is, FGG as applied by law enforcement to criminal investigations; hence, investigative FGG or iFGG. We delineate its steps, compare and contrast it with other investigative techniques involving genetic evidence, and contextualize its use within criminal investigations. This characterization is a critical input to future studies regarding the legal status of iFGG and its implications on the right to genetic privacy.

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          Most cited references60

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          The complete sequence of a human genome*

          Since its initial release in 2000, the human reference genome has covered only the euchromatic fraction of the genome, leaving important heterochromatic regions unfinished. Addressing the remaining 8% of the genome, the Telomere-to-Telomere (T2T) Consortium presents a complete 3.055 billion base pair (bp) sequence of a human genome, T2T-CHM13, that includes gapless assemblies for all chromosomes except Y, corrects errors in the prior references, and introduces nearly 200 million bp of sequence containing 1,956 gene predictions, 99 of which are predicted to be protein coding. The completed regions include all centromeric satellite arrays, recent segmental duplications, and the short arms of all five acrocentric chromosomes, unlocking these complex regions of the genome to variational and functional studies. Twenty years after the initial drafts, a truly complete sequence of a human genome reveals what has been missing.
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            A vision for the future of genomics research.

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              • Record: found
              • Abstract: not found
              • Article: not found

              Individual-specific ‘fingerprints’ of human DNA

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                Author and article information

                Contributors
                Journal
                Forensic Sci Int Synerg
                Forensic Sci Int Synerg
                Forensic Science International: Synergy
                Elsevier
                2589-871X
                08 February 2024
                2024
                08 February 2024
                : 8
                : 100460
                Affiliations
                [a ]Center for Law and Digital Technologies (eLaw), Institute for the Interdisciplinary Study of the Law, Leiden Law School, Leiden University, Kamerlingh Onnes Building, Steenschuur 25, 2311 ES, Leiden, the Netherlands
                [b ]New York State Police Crime Laboratory System, Forensic Investigation Center, 1220 Washington Avenue, Building #30, Albany, NY, 12226-3000, USA
                [c ]Swedish Police Authority, National Forensic Centre, SE-581 94, Linköping, Sweden
                [d ]Baylor College of Medicine, Center for Medical Ethics and Health Policy, Houston, TX, 77030, USA
                [e ]Department of Physics, Chemistry and Biology, Linköping University, Sweden
                Author notes
                []Corresponding author. o.m.tuazon@ 123456law.leidenuniv.nl
                Article
                S2589-871X(24)00007-X 100460
                10.1016/j.fsisyn.2024.100460
                10876674
                38380276
                10c0d6ef-a12d-45a8-a9fa-94845faac1e1
                © 2024 Published by Elsevier B.V.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 8 December 2023
                : 7 February 2024
                : 7 February 2024
                Categories
                General

                forensic dna,forensic genealogy,genetic genealogy,investigative genetic genealogy (igg),forensic genetic genealogy (fgg),forensic investigative genetic genealogy (figg),investigative forensic genetic genealogy (ifgg)

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