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PUBMED FOR HANDHELDS

Journal Abstract Search


947 related items for PubMed ID: 28938154

  • 1. 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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  • 2. Developmental validation of the MiSeq FGx Forensic Genomics System for Targeted Next Generation Sequencing in Forensic DNA Casework and Database Laboratories.
    Jäger AC, Alvarez ML, Davis CP, Guzmán E, Han Y, Way L, Walichiewicz P, Silva D, Pham N, Caves G, Bruand J, Schlesinger F, Pond SJK, Varlaro J, Stephens KM, Holt CL.
    Forensic Sci Int Genet; 2017 May; 28():52-70. PubMed ID: 28171784
    [Abstract] [Full Text] [Related]

  • 3. 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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  • 4. Evaluation of the Illumina ForenSeq™ DNA Signature Prep Kit - MPS forensic application for the MiSeq FGx™ benchtop sequencer.
    Xavier C, Parson W.
    Forensic Sci Int Genet; 2017 May; 28():188-194. PubMed ID: 28279935
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  • 8. 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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  • 11. Population and performance analyses of four major populations with Illumina's FGx Forensic Genomics System.
    Churchill JD, Novroski NMM, King JL, Seah LH, Budowle B.
    Forensic Sci Int Genet; 2017 Sep; 30():81-92. PubMed ID: 28651097
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  • 13. Comparative tolerance of two massively parallel sequencing systems to common PCR inhibitors.
    Elwick K, Zeng X, King J, Budowle B, Hughes-Stamm S.
    Int J Legal Med; 2018 Jul; 132(4):983-995. PubMed ID: 28956146
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  • 14. Performance and characterization of 94 identity-informative SNPs in Northern Han Chinese using ForenSeq ™ DNA signature prep kit.
    Guo F, Liu Z, Long G, Zhang B, Liu D, Yu S.
    J Forensic Leg Med; 2024 Apr; 103():102678. PubMed ID: 38522119
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  • 16. Inter-laboratory study on standardized MPS libraries: evaluation of performance, concordance, and sensitivity using mixtures and degraded DNA.
    Müller P, Sell C, Hadrys T, Hedman J, Bredemeyer S, Laurent FX, Roewer L, Achtruth S, Sidstedt M, Sijen T, Trimborn M, Weiler N, Willuweit S, Bastisch I, Parson W, SeqForSTR-Consortium.
    Int J Legal Med; 2020 Jan; 134(1):185-198. PubMed ID: 31745634
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  • 17. A novel forensic panel of 186-plex SNPs and 123-plex STR loci based on massively parallel sequencing.
    Miao X, Shen Y, Gong X, Yu H, Li B, Chang L, Wang Y, Fan J, Liang Z, Tan B, Li S, Zhang B.
    Int J Legal Med; 2021 May; 135(3):709-718. PubMed ID: 32851473
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  • 18. Developmental validation of the ForenSeq MainstAY kit, MiSeq FGx sequencing system and ForenSeq Universal Analysis Software.
    Stephens KM, Barta R, Fleming K, Perez JC, Wu SF, Snedecor J, Holt CL, LaRue B, Budowle B.
    Forensic Sci Int Genet; 2023 May; 64():102851. PubMed ID: 36907074
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  • 19. Filipino DNA variation at 12 X-chromosome short tandem repeat markers.
    Salvador JM, Apaga DLT, Delfin FC, Calacal GC, Dennis SE, De Ungria MCA.
    Forensic Sci Int Genet; 2018 Sep; 36():e8-e12. PubMed ID: 29909139
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  • 20. Inter-laboratory validation study of the ForenSeq™ DNA Signature Prep Kit.
    Köcher S, Müller P, Berger B, Bodner M, Parson W, Roewer L, Willuweit S, DNASeqEx Consortium.
    Forensic Sci Int Genet; 2018 Sep; 36():77-85. PubMed ID: 29945120
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