BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 23736940)

  • 21. SNP typing using the HID-Ion AmpliSeq™ Identity Panel in a southern Chinese population.
    Li R; Zhang C; Li H; Wu R; Li H; Tang Z; Zhen C; Ge J; Peng D; Wang Y; Chen H; Sun H
    Int J Legal Med; 2018 Jul; 132(4):997-1006. PubMed ID: 29046953
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Evaluation of Y chromosomal SNP haplogrouping in the HID-Ion AmpliSeq™ Identity Panel.
    Ochiai E; Minaguchi K; Nambiar P; Kakimoto Y; Satoh F; Nakatome M; Miyashita K; Osawa M
    Leg Med (Tokyo); 2016 Sep; 22():58-61. PubMed ID: 27591541
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Massively parallel sequencing of 231 autosomal SNPs with a custom panel: a SNP typing assay developed for human identification with Ion Torrent PGM.
    Zhang S; Bian Y; Chen A; Zheng H; Gao Y; Hou Y; Li C
    Forensic Sci Res; 2017; 2(1):26-33. PubMed ID: 30483616
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Massively parallel sequencing of forensic STRs and SNPs using the Illumina
    Guo F; Yu J; Zhang L; Li J
    Forensic Sci Int Genet; 2017 Nov; 31():135-148. PubMed ID: 28938154
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Developmental validation of a custom panel including 273 SNPs for forensic application using Ion Torrent PGM.
    Zhang S; Bian Y; Chen A; Zheng H; Gao Y; Hou Y; Li C
    Forensic Sci Int Genet; 2017 Mar; 27():50-57. PubMed ID: 27951431
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Second-generation sequencing of forensic STRs using the Ion Torrent™ HID STR 10-plex and the Ion PGM™.
    Fordyce SL; Mogensen HS; Børsting C; Lagacé RE; Chang CW; Rajagopalan N; Morling N
    Forensic Sci Int Genet; 2015 Jan; 14():132-40. PubMed ID: 25450784
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Target capture enrichment of nuclear SNP markers for massively parallel sequencing of degraded and mixed samples.
    Bose N; Carlberg K; Sensabaugh G; Erlich H; Calloway C
    Forensic Sci Int Genet; 2018 May; 34():186-196. PubMed ID: 29524767
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The MASTiFF panel-a versatile multiple-allele SNP test for forensics.
    Phillips C; Manzo L; de la Puente M; Fondevila M; Lareu MV
    Int J Legal Med; 2020 Mar; 134(2):441-450. PubMed ID: 31863187
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Evaluation of the iPLEX® Sample ID Plus Panel designed for the Sequenom MassARRAY® system. A SNP typing assay developed for human identification and sample tracking based on the SNPforID panel.
    Johansen P; Andersen JD; Børsting C; Morling N
    Forensic Sci Int Genet; 2013 Sep; 7(5):482-7. PubMed ID: 23948317
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Forensic characterization of Brazilian regional populations through massive parallel sequencing of 124 SNPs included in HID ion Ampliseq Identity Panel.
    Avila E; Felkl AB; Graebin P; Nunes CP; Alho CS
    Forensic Sci Int Genet; 2019 May; 40():74-84. PubMed ID: 30780121
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Analysis of complex DNA mixtures using massively parallel sequencing of SNPs with low minor allele frequencies.
    Petrovick MS; Boettcher T; Fremont-Smith P; Peragallo C; Ricke DO; Watkins J; Schwoebel E
    Forensic Sci Int Genet; 2020 May; 46():102234. PubMed ID: 32018060
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Typing of 48 autosomal SNPs and amelogenin with GenPlex SNP genotyping system in forensic genetics.
    Tomas C; Stangegaard M; Børsting C; Hansen AJ; Morling N;
    Forensic Sci Int Genet; 2008 Dec; 3(1):1-6. PubMed ID: 19083859
    [TBL] [Abstract][Full Text] [Related]  

  • 35. DNA typing from skeletal remains: a comparison between capillary electrophoresis and massively parallel sequencing platforms.
    Liu Z; Gao L; Zhang J; Fan Q; Chen M; Cheng F; Li W; Shi L; Zhang X; Zhang J; Zhang G; Yan J
    Int J Legal Med; 2020 Nov; 134(6):2029-2035. PubMed ID: 32507908
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Sequence-based US population data for the SE33 locus.
    Borsuk LA; Gettings KB; Steffen CR; Kiesler KM; Vallone PM
    Electrophoresis; 2018 Nov; 39(21):2694-2701. PubMed ID: 29736954
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Evaluation of the Early Access STR Kit v1 on the Ion Torrent PGM™ platform.
    Guo F; Zhou Y; Liu F; Yu J; Song H; Shen H; Zhao B; Jia F; Hou G; Jiang X
    Forensic Sci Int Genet; 2016 Jul; 23():111-120. PubMed ID: 27082757
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The FORCE Panel: An All-in-One SNP Marker Set for Confirming Investigative Genetic Genealogy Leads and for General Forensic Applications.
    Tillmar A; Sturk-Andreaggi K; Daniels-Higginbotham J; Thomas JT; Marshall C
    Genes (Basel); 2021 Dec; 12(12):. PubMed ID: 34946917
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Blind study evaluation illustrates utility of the Ion PGM™ system for use in human identity DNA typing.
    Churchill JD; Chang J; Ge J; Rajagopalan N; Wootton SC; Chang CW; Lagacé R; Liao W; King JL; Budowle B
    Croat Med J; 2015 Jun; 56(3):218-29. PubMed ID: 26088846
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Evaluation of the Precision ID Identity Panel for the Ion Torrent
    Meiklejohn KA; Robertson JM
    Forensic Sci Int Genet; 2017 Nov; 31():48-56. PubMed ID: 28843089
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.