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213 related items for PubMed ID: 30374565

  • 1. Massively parallel sequencing analysis of nondegraded and degraded DNA mixtures using the ForenSeq™ system in combination with EuroForMix software.
    Hwa HL, Wu MY, Chung WC, Ko TM, Lin CP, Yin HI, Lee TT, Lee JC.
    Int J Legal Med; 2019 Jan; 133(1):25-37. PubMed ID: 30374565
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  • 2. Analysis of nondegraded and degraded DNA mixtures of close relatives using massively parallel sequencing.
    Hwa HL, Wu MY, Lee JC, Yin HI, Hsu PM, Li SF, Hwu WL, Su CW.
    Leg Med (Tokyo); 2020 Feb; 42():101631. PubMed ID: 31751795
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  • 3. Massively parallel sequencing of forensic STRs and SNPs using the Illumina® ForenSeq™ DNA Signature Prep Kit on the MiSeq FGx™ Forensic Genomics System.
    Guo F, Yu J, Zhang L, Li J.
    Forensic Sci Int Genet; 2017 Nov; 31():135-148. PubMed ID: 28938154
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  • 5. A 1204-single nucleotide polymorphism and insertion-deletion polymorphism panel for massively parallel sequencing analysis of DNA mixtures.
    Hwa HL, Chung WC, Chen PL, Lin CP, Li HY, Yin HI, Lee JC.
    Forensic Sci Int Genet; 2018 Jan; 32():94-101. PubMed ID: 29128546
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  • 6. Application of a probabilistic genotyping software to MPS mixture STR data is supported by similar trends in LRs compared with CE data.
    Benschop CCG, van der Gaag KJ, de Vreede J, Backx AJ, de Leeuw RH, Zuñiga S, Hoogenboom J, de Knijff P, Sijen T.
    Forensic Sci Int Genet; 2021 May; 52():102489. PubMed ID: 33677249
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  • 7. Mixture deconvolution by massively parallel sequencing of microhaplotypes.
    Bennett L, Oldoni F, Long K, Cisana S, Madella K, Wootton S, Chang J, Hasegawa R, Lagacé R, Kidd KK, Podini D.
    Int J Legal Med; 2019 May; 133(3):719-729. PubMed ID: 30758713
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  • 8. Open source software EuroForMix can be used to analyse complex SNP mixtures.
    Bleka Ø, Eduardoff M, Santos C, Phillips C, Parson W, Gill P.
    Forensic Sci Int Genet; 2017 Nov; 31():105-110. PubMed ID: 28942111
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  • 10. Flanking region variation of ForenSeq™ DNA Signature Prep Kit STR and SNP loci in Yavapai Native Americans.
    Wendt FR, King JL, Novroski NMM, Churchill JD, Ng J, Oldt RF, McCulloh KL, Weise JA, Smith DG, Kanthaswamy S, Budowle B.
    Forensic Sci Int Genet; 2017 May; 28():146-154. PubMed ID: 28273507
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  • 14. Global patterns of STR sequence variation: Sequencing the CEPH human genome diversity panel for 58 forensic STRs using the Illumina ForenSeq DNA Signature Prep Kit.
    Phillips C, Devesse L, Ballard D, van Weert L, de la Puente M, Melis S, Álvarez Iglesias V, Freire-Aradas A, Oldroyd N, Holt C, Syndercombe Court D, Carracedo Á, Lareu MV.
    Electrophoresis; 2018 Nov; 39(21):2708-2724. PubMed ID: 30101987
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  • 15. Improved individual identification in DNA mixtures of unrelated or related contributors through massively parallel sequencing.
    Liu Z, Wu E, Li R, Liu J, Zang Y, Cong B, Wu R, Xie B, Sun H.
    Forensic Sci Int Genet; 2024 Sep; 72():103078. PubMed ID: 38889491
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  • 18. A preliminary assessment of the ForenSeq™ FGx System: next generation sequencing of an STR and SNP multiplex.
    Silvia AL, Shugarts N, Smith J.
    Int J Legal Med; 2017 Jan; 131(1):73-86. PubMed ID: 27785563
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  • 20. Characterization of 58 STRs and 94 SNPs with the ForenSeq™ DNA signature prep kit in Mexican-Mestizos from the Monterrey city (Northeast, Mexico).
    Aguilar-Velázquez JA, Duran-Salazar MÁ, Córdoba-Mercado MF, Coronado-Avila CE, Salas-Salas O, Martinez-Cortés G, Casals F, Calafell F, Ramos-González B, Rangel-Villalobos H.
    Mol Biol Rep; 2022 Aug; 49(8):7601-7609. PubMed ID: 35657453
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