Literature DB >> 31863187

The MASTiFF panel-a versatile multiple-allele SNP test for forensics.

C Phillips1, L Manzo2, M de la Puente2, M Fondevila2, M V Lareu2.   

Abstract

Forensic identification tests often need recourse to markers that can successfully type highly degraded DNA, and binary single nucleotide polymorphisms (SNPs) have become the variants of choice for such analyses because of their short amplified fragment lengths. The two main drawbacks of SNPs are their reduced power of discrimination per marker compared with mainstream forensic STRs and an inability to robustly detect mixed DNA-particularly using capillary electrophoresis genotyping systems such as SNaPshot™, where the dye signals are much more imbalanced than those of STR profiles. This study compiled a compact set of multiple-allele SNPs consisting of loci that had three or four nucleotide variants at the same site in order to address the lack of mixture detection capability with binary SNP tests, as well as improving levels of polymorphism per SNP by transitioning to a maximum of six or ten genotypes per locus. We report the development and optimisation of a SNaPshot-based forensic test comprising 27 tri-allelic and 2 tetra-allelic SNPs, which we named MASTiFF: a multiple-allele SNP test for forensics. Assessments of the MASTiFF panel's levels of discrimination power in the five main population groups indicate random match probabilities ranging from 10-15 down to 10-20-improving the levels possible from an equivalent number of binary SNPs. The SNaPshot test was able to detect simple mixtures successfully with more than two alleles observed in 30% of SNPs. From allele frequency data, it is estimated that more than two alleles will be present in at least one MASTiFF SNP in 99.8% of two-person mixtures, making this panel an ideal supplementary test when SNPs are chosen for the analysis of degraded forensic DNA.

Entities:  

Keywords:  Mixed DNA; Multiple-allele SNPs; SNaPshot; Single nucleotide polymorphisms (SNPs)

Mesh:

Substances:

Year:  2019        PMID: 31863187     DOI: 10.1007/s00414-019-02233-8

Source DB:  PubMed          Journal:  Int J Legal Med        ISSN: 0937-9827            Impact factor:   2.686


  43 in total

1.  Typing short amplicon binary polymorphisms: supplementary SNP and Indel genetic information in the analysis of highly degraded skeletal remains.

Authors:  C Romanini; M L Catelli; A Borosky; R Pereira; M Romero; M Salado Puerto; C Phillips; M Fondevila; A Freire; C Santos; A Carracedo; M V Lareu; L Gusmao; C M Vullo
Journal:  Forensic Sci Int Genet       Date:  2011-11-25       Impact factor: 4.882

2.  Secondary uses and the governance of de-identified data: lessons from the human genome diversity panel.

Authors:  Stephanie M Fullerton; Sandra S-J Lee
Journal:  BMC Med Ethics       Date:  2011-09-26       Impact factor: 2.652

Review 3.  Genetics and genomics of core short tandem repeat loci used in human identity testing.

Authors:  John M Butler
Journal:  J Forensic Sci       Date:  2006-03       Impact factor: 1.832

4.  DNA commission of the International Society of Forensic Genetics: Recommendations on the interpretation of mixtures.

Authors:  P Gill; C H Brenner; J S Buckleton; A Carracedo; M Krawczak; W R Mayr; N Morling; M Prinz; P M Schneider; B S Weir
Journal:  Forensic Sci Int       Date:  2006-06-05       Impact factor: 2.395

5.  Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel.

Authors:  C Phillips; R Fang; D Ballard; M Fondevila; C Harrison; F Hyland; E Musgrave-Brown; C Proff; E Ramos-Luis; B Sobrino; A Carracedo; M R Furtado; D Syndercombe Court; P M Schneider
Journal:  Forensic Sci Int Genet       Date:  2007-03-23       Impact factor: 4.882

6.  A new SNP assay for identification of highly degraded human DNA.

Authors:  A Freire-Aradas; M Fondevila; A-K Kriegel; C Phillips; P Gill; L Prieto; P M Schneider; A Carracedo; M V Lareu
Journal:  Forensic Sci Int Genet       Date:  2011-09-09       Impact factor: 4.882

7.  Inter-laboratory evaluation of SNP-based forensic identification by massively parallel sequencing using the Ion PGM™.

Authors:  M Eduardoff; C Santos; M de la Puente; T E Gross; M Fondevila; C Strobl; B Sobrino; D Ballard; P M Schneider; Á Carracedo; M V Lareu; W Parson; C Phillips
Journal:  Forensic Sci Int Genet       Date:  2015-04-15       Impact factor: 4.882

8.  Development and validation of the EUROFORGEN NAME (North African and Middle Eastern) ancestry panel.

Authors:  V Pereira; A Freire-Aradas; D Ballard; C Børsting; V Diez; P Pruszkowska-Przybylska; J Ribeiro; N M Achakzai; A Aliferi; O Bulbul; M D Perez Carceles; S Triki-Fendri; A Rebai; D Syndercombe Court; N Morling; M V Lareu; Á Carracedo; C Phillips
Journal:  Forensic Sci Int Genet       Date:  2019-06-15       Impact factor: 4.882

Review 9.  Forensic genetic analysis of bio-geographical ancestry.

Authors:  Chris Phillips
Journal:  Forensic Sci Int Genet       Date:  2015-05-19       Impact factor: 4.882

10.  The Simons Genome Diversity Project: 300 genomes from 142 diverse populations.

Authors:  Swapan Mallick; Heng Li; Mark Lipson; Iain Mathieson; Melissa Gymrek; Fernando Racimo; Mengyao Zhao; Niru Chennagiri; Susanne Nordenfelt; Arti Tandon; Pontus Skoglund; Iosif Lazaridis; Sriram Sankararaman; Qiaomei Fu; Nadin Rohland; Gabriel Renaud; Yaniv Erlich; Thomas Willems; Carla Gallo; Jeffrey P Spence; Yun S Song; Giovanni Poletti; Francois Balloux; George van Driem; Peter de Knijff; Irene Gallego Romero; Aashish R Jha; Doron M Behar; Claudio M Bravi; Cristian Capelli; Tor Hervig; Andres Moreno-Estrada; Olga L Posukh; Elena Balanovska; Oleg Balanovsky; Sena Karachanak-Yankova; Hovhannes Sahakyan; Draga Toncheva; Levon Yepiskoposyan; Chris Tyler-Smith; Yali Xue; M Syafiq Abdullah; Andres Ruiz-Linares; Cynthia M Beall; Anna Di Rienzo; Choongwon Jeong; Elena B Starikovskaya; Ene Metspalu; Jüri Parik; Richard Villems; Brenna M Henn; Ugur Hodoglugil; Robert Mahley; Antti Sajantila; George Stamatoyannopoulos; Joseph T S Wee; Rita Khusainova; Elza Khusnutdinova; Sergey Litvinov; George Ayodo; David Comas; Michael F Hammer; Toomas Kivisild; William Klitz; Cheryl A Winkler; Damian Labuda; Michael Bamshad; Lynn B Jorde; Sarah A Tishkoff; W Scott Watkins; Mait Metspalu; Stanislav Dryomov; Rem Sukernik; Lalji Singh; Kumarasamy Thangaraj; Svante Pääbo; Janet Kelso; Nick Patterson; David Reich
Journal:  Nature       Date:  2016-09-21       Impact factor: 49.962

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  1 in total

1.  Applications of massively parallel sequencing in forensic genetics.

Authors:  Thássia Mayra Telles Carratto; Vitor Matheus Soares Moraes; Tamara Soledad Frontanilla Recalde; Maria Luiza Guimarães de Oliveira; Celso Teixeira Mendes-Junior
Journal:  Genet Mol Biol       Date:  2022-09-19       Impact factor: 2.087

  1 in total

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