These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

93 related articles for article (PubMed ID: 18348287)

  • 1. Large scale DNA sequencing: new challenges emerge--the 2007 Human Genome Variation Society scientific meeting.
    Oetting WS
    Hum Mutat; 2008 May; 29(5):765-8. PubMed ID: 18348287
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Impact of next generation sequencing: the 2009 Human Genome Variation Society Scientific Meeting.
    Oetting WS
    Hum Mutat; 2010 Apr; 31(4):500-3. PubMed ID: 20127974
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exploring the functional consequences of genomic variation: the 2010 Human Genome Variation Society Scientific Meeting.
    Oetting WS
    Hum Mutat; 2011 Apr; 32(4):486-90. PubMed ID: 21412951
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical genetics & human genome variation: the 2008 Human Genome Variation Society scientific meeting.
    Oetting WS
    Hum Mutat; 2009 May; 30(5):852-6. PubMed ID: 19260058
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Exome and genome analysis as a tool for disease identification and treatment: the 2011 Human Genome Variation Society scientific meeting.
    Oetting WS
    Hum Mutat; 2012 Mar; 33(3):586-90. PubMed ID: 22213110
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The 2006 Human Genome Variation Society scientific meeting.
    Oetting WS
    Hum Mutat; 2007 May; 28(5):517-21. PubMed ID: 17357128
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical Interpretation of Variants from Next-Generation Sequencing: The 2016 Scientific Meeting of the Human Genome Variation Society.
    Oetting WS; Brookes AJ; Béroud C; Taschner PE
    Hum Mutat; 2016 Oct; 37(10):1110-3. PubMed ID: 27492570
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinically relevant variants - identifying, collecting, interpreting, and disseminating: the 2013 annual scientific meeting of the Human Genome Variation Society.
    Stanley CM; Sunyaev SR; Greenblatt MS; Oetting WS
    Hum Mutat; 2014 Apr; 35(4):505-10. PubMed ID: 24470180
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 2005 Human Genome Variation Society Scientific Meeting.
    Oetting WS
    Hum Mutat; 2006 Mar; 27(3):286-9. PubMed ID: 16419082
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Characterizing and interpreting genetic variation from personal genome sequencing.
    Johansson AC; Feuk L
    Methods Mol Biol; 2012; 838():343-67. PubMed ID: 22228021
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Whole genome sequencing.
    Ng PC; Kirkness EF
    Methods Mol Biol; 2010; 628():215-26. PubMed ID: 20238084
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Perspectives and challenges of emerging single-molecule DNA sequencing technologies.
    Xu M; Fujita D; Hanagata N
    Small; 2009 Dec; 5(23):2638-49. PubMed ID: 19904762
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Non-Coding Variation: The 2016 Annual Scientific Meeting of the Human Genome Variation Society.
    Oetting WS; Béroud C; Brenner SE; Greenblatt M; Karchin R; Mooney SD; Sunyaev S
    Hum Mutat; 2017 Apr; 38(4):460-463. PubMed ID: 28054414
    [No Abstract]   [Full Text] [Related]  

  • 14. Sequence Variant Descriptions: HGVS Nomenclature and Mutalyzer.
    den Dunnen JT
    Curr Protoc Hum Genet; 2016 Jul; 90():7.13.1-7.13.19. PubMed ID: 27367167
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Structural variation analysis with strobe reads.
    Ritz A; Bashir A; Raphael BJ
    Bioinformatics; 2010 May; 26(10):1291-8. PubMed ID: 20378554
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Keeping up with the next generation: massively parallel sequencing in clinical diagnostics.
    ten Bosch JR; Grody WW
    J Mol Diagn; 2008 Nov; 10(6):484-92. PubMed ID: 18832462
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pooled-DNA Sequencing for Elucidating New Genomic Risk Factors, Rare Variants Underlying Alzheimer's Disease.
    Jin SC; Benitez BA; Deming Y; Cruchaga C
    Methods Mol Biol; 2016; 1303():299-314. PubMed ID: 26235075
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Variations in the Genome: The Mutation Detection 2015 Meeting on Detection, Genome Sequencing, and Interpretation.
    Torres-Español M; Anvar SY; Sobrido MJ
    Hum Mutat; 2016 Oct; 37(10):1106-9. PubMed ID: 27363592
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The 2004 Human Genome Variation Society scientific meeting.
    Oetting WS; Tabone T
    Hum Mutat; 2005 Aug; 26(2):160-3. PubMed ID: 15971230
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The application of the HapMap to diabetic nephropathy and other causes of chronic renal failure.
    Iyengar SK; Adler SG
    Semin Nephrol; 2007 Mar; 27(2):223-36. PubMed ID: 17418690
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.