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Journal Abstract Search

406 related items for PubMed ID: 27208666

  • 1. Inter-laboratory evaluation of the EUROFORGEN Global ancestry-informative SNP panel by massively parallel sequencing using the Ion PGM™.
    Eduardoff M, Gross TE, Santos C, de la Puente M, Ballard D, Strobl C, Børsting C, Morling N, Fusco L, Hussing C, Egyed B, Souto L, Uacyisrael J, Syndercombe Court D, Carracedo Á, Lareu MV, Schneider PM, Parson W, Phillips C, EUROFORGEN-NoE Consortium, Parson W, Phillips C.
    Forensic Sci Int Genet; 2016 Jul; 23():178-189. PubMed ID: 27208666
    [Abstract] [Full Text] [Related]

  • 2. Evaluation of the Qiagen 140-SNP forensic identification multiplex for massively parallel sequencing.
    de la Puente M, Phillips C, Santos C, Fondevila M, Carracedo Á, Lareu MV.
    Forensic Sci Int Genet; 2017 May; 28():35-43. PubMed ID: 28160618
    [Abstract] [Full Text] [Related]

  • 3. Inter-laboratory evaluation of SNP-based forensic identification by massively parallel sequencing using the Ion PGM™.
    Eduardoff M, Santos C, de la Puente M, Gross TE, Fondevila M, Strobl C, Sobrino B, Ballard D, Schneider PM, Carracedo Á, Lareu MV, Parson W, Phillips C.
    Forensic Sci Int Genet; 2015 Jul; 17():110-121. PubMed ID: 25955683
    [Abstract] [Full Text] [Related]

  • 4. Evaluation of the Precision ID Ancestry Panel for crime case work: A SNP typing assay developed for typing of 165 ancestral informative markers.
    Pereira V, Mogensen HS, Børsting C, Morling N.
    Forensic Sci Int Genet; 2017 May; 28():138-145. PubMed ID: 28273506
    [Abstract] [Full Text] [Related]

  • 5. Assessment of the Precision ID Ancestry panel.
    Al-Asfi M, McNevin D, Mehta B, Power D, Gahan ME, Daniel R.
    Int J Legal Med; 2018 Nov; 132(6):1581-1594. PubMed ID: 29556719
    [Abstract] [Full Text] [Related]

  • 6. Next generation sequencing of SNPs using the HID-Ion AmpliSeq™ Identity Panel on the Ion Torrent PGM™ platform.
    Guo F, Zhou Y, Song H, Zhao J, Shen H, Zhao B, Liu F, Jiang X.
    Forensic Sci Int Genet; 2016 Nov; 25():73-84. PubMed ID: 27500651
    [Abstract] [Full Text] [Related]

  • 7. Allele frequencies and other forensic parameters of the HID-Ion AmpliSeq™ Identity Panel markers in Basques using the Ion Torrent PGM™ platform.
    García O, Soto A, Yurrebaso I.
    Forensic Sci Int Genet; 2017 May; 28():e8-e10. PubMed ID: 28342798
    [Abstract] [Full Text] [Related]

  • 8. MAPlex - A massively parallel sequencing ancestry analysis multiplex for Asia-Pacific populations.
    Phillips C, McNevin D, Kidd KK, Lagacé R, Wootton S, de la Puente M, Freire-Aradas A, Mosquera-Miguel A, Eduardoff M, Gross T, Dagostino L, Power D, Olson S, Hashiyada M, Oz C, Parson W, Schneider PM, Lareu MV, Daniel R.
    Forensic Sci Int Genet; 2019 Sep; 42():213-226. PubMed ID: 31377479
    [Abstract] [Full Text] [Related]

  • 9. Effects of the Ion PGM™ Hi-Q™ sequencing chemistry on sequence data quality.
    Churchill JD, King JL, Chakraborty R, Budowle B.
    Int J Legal Med; 2016 Sep; 130(5):1169-80. PubMed ID: 27025714
    [Abstract] [Full Text] [Related]

  • 10. Development and Evaluation of the Ancestry Informative Marker Panel of the VISAGE Basic Tool.
    de la Puente M, Ruiz-Ramírez J, Ambroa-Conde A, Xavier C, Pardo-Seco J, Álvarez-Dios J, Freire-Aradas A, Mosquera-Miguel A, Gross TE, Cheung EYY, Branicki W, Nothnagel M, Parson W, Schneider PM, Kayser M, Carracedo Á, Lareu MV, Phillips C, On Behalf Of The Visage Consortium.
    Genes (Basel); 2021 Aug 22; 12(8):. PubMed ID: 34440458
    [Abstract] [Full Text] [Related]

  • 11. Comparison of manual and automated AmpliSeq™ workflows in the typing of a Somali population with the Precision ID Identity Panel.
    van der Heijden S, de Oliveira SJ, Kampmann ML, Børsting C, Morling N.
    Forensic Sci Int Genet; 2017 Nov 22; 31():118-125. PubMed ID: 28938152
    [Abstract] [Full Text] [Related]

  • 12. Frequencies of the precision ID ancestry panel markers in Basques using the Ion Torrent PGMTM platform.
    García O, Ajuriagerra JA, Alday A, Alonso S, Pérez JA, Soto A, Uriarte I, Yurrebaso I.
    Forensic Sci Int Genet; 2017 Nov 22; 31():e1-e4. PubMed ID: 28935228
    [Abstract] [Full Text] [Related]

  • 13. 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 22; 28():52-70. PubMed ID: 28171784
    [Abstract] [Full Text] [Related]

  • 14. The QIAGEN 140-locus single-nucleotide polymorphism (SNP) panel for forensic identification using massively parallel sequencing (MPS): an evaluation and a direct-to-PCR trial.
    Avent I, Kinnane AG, Jones N, Petermann I, Daniel R, Gahan ME, McNevin D.
    Int J Legal Med; 2019 May 22; 133(3):677-688. PubMed ID: 30519731
    [Abstract] [Full Text] [Related]

  • 15. 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 22; 31():135-148. PubMed ID: 28938154
    [Abstract] [Full Text] [Related]

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