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Journal Abstract Search

757 related items for PubMed ID: 28126691

  • 1. Performance and concordance of the ForenSeq™ system for autosomal and Y chromosome short tandem repeat sequencing of reference-type specimens.
    Just RS, Moreno LI, Smerick JB, Irwin JA.
    Forensic Sci Int Genet; 2017 May; 28():1-9. PubMed ID: 28126691
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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
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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. Evaluation of the Illumina(®) Beta Version ForenSeq™ DNA Signature Prep Kit for use in genetic profiling.
    Churchill JD, Schmedes SE, King JL, Budowle B.
    Forensic Sci Int Genet; 2016 Jan; 20():20-29. PubMed ID: 26433485
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  • 7. 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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  • 8. The Danish STR sequence database: duplicate typing of 363 Danes with the ForenSeq™ DNA Signature Prep Kit.
    Hussing C, Bytyci R, Huber C, Morling N, Børsting C.
    Int J Legal Med; 2019 Mar; 133(2):325-334. PubMed ID: 29797283
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  • 9. 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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  • 10. Investigation into the sequence structure of 23 Y chromosomal STR loci using massively parallel sequencing.
    Kwon SY, Lee HY, Kim EH, Lee EY, Shin KJ.
    Forensic Sci Int Genet; 2016 Nov; 25():132-141. PubMed ID: 27591816
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  • 11. Sequencing of autosomal, mitochondrial and Y-chromosomal forensic markers in the People of the British Isles cohort detects population structure dominated by patrilineages.
    Huszar TI, Bodmer WF, Hutnik K, Wetton JH, Jobling MA.
    Forensic Sci Int Genet; 2022 Jul; 59():102725. PubMed ID: 35640311
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  • 12. Genetic analysis of Southern Brazil subjects using the PowerSeq™ AUTO/Y system for short tandem repeat sequencing.
    Silva DSBS, Sawitzki FR, Scheible MKR, Bailey SF, Alho CS, Faith SA.
    Forensic Sci Int Genet; 2018 Mar; 33():129-135. PubMed ID: 29275088
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  • 14. A closer look at Verogen's Forenseq™ DNA Signature Prep kit autosomal and Y-STR data for streamlined analysis of routine reference samples.
    Moreno LI, Galusha MB, Just R.
    Electrophoresis; 2018 Nov; 39(21):2685-2693. PubMed ID: 30025170
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  • 16. Simultaneous sequencing of 102 Y-STRs on Ion Torrent ™ GeneStudio ™ S5 System.
    Guo F, Jing G, Lang Y, Liu Z, Yu S.
    Forensic Sci Int Genet; 2024 Jul; 71():103059. PubMed ID: 38749212
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  • 17. 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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  • 18. 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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  • 19. Concordance study on Y-STRs typing between SeqStudio™ genetic analyzer for HID and MiSeq™ FGx forensic genomics system.
    Soldati G, Turrina S, Treccani M, Saccardo C, Ausania F, De Leo D.
    Mol Biol Rep; 2023 Dec; 50(12):9779-9789. PubMed ID: 37812349
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