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 *

244 related articles for article (PubMed ID: 20127974)

  • 21. 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]  

  • 22. Opportunities and challenges of whole-genome and -exome sequencing.
    Petersen BS; Fredrich B; Hoeppner MP; Ellinghaus D; Franke A
    BMC Genet; 2017 Feb; 18(1):14. PubMed ID: 28193154
    [TBL] [Abstract][Full Text] [Related]  

  • 23. The development and impact of 454 sequencing.
    Rothberg JM; Leamon JH
    Nat Biotechnol; 2008 Oct; 26(10):1117-24. PubMed ID: 18846085
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Understanding human genetic variation in the era of high-throughput sequencing.
    Knight JC
    EMBO Rep; 2010 Sep; 11(9):650-2. PubMed ID: 20725090
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Clinical exome sequencing in neurogenetic and neuropsychiatric disorders.
    Fogel BL; Lee H; Strom SP; Deignan JL; Nelson SF
    Ann N Y Acad Sci; 2016 Feb; 1366(1):49-60. PubMed ID: 26250888
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Clinical Implementation and Validation of Automated Human Genome Variation Society (HGVS) Nomenclature System for Next-Generation Sequencing-Based Assays for Cancer.
    Callenberg KM; Santana-Santos L; Chen L; Ernst WL; De Moura MB; Nikiforov YE; Nikiforova MN; Roy S
    J Mol Diagn; 2018 Sep; 20(5):628-634. PubMed ID: 29936258
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genomics of medulloblastoma: from Giemsa-banding to next-generation sequencing in 20 years.
    Northcott PA; Rutka JT; Taylor MD
    Neurosurg Focus; 2010 Jan; 28(1):E6. PubMed ID: 20043721
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The impact of next-generation sequencing on genomics.
    Zhang J; Chiodini R; Badr A; Zhang G
    J Genet Genomics; 2011 Mar; 38(3):95-109. PubMed ID: 21477781
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The next-generation sequencing revolution and its impact on genomics.
    Koboldt DC; Steinberg KM; Larson DE; Wilson RK; Mardis ER
    Cell; 2013 Sep; 155(1):27-38. PubMed ID: 24074859
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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]  

  • 32. [Human genome sequencing--next generation technology or will the routine sequencing of human genome be possible?].
    Pospísilová S; Tichý B; Mayer J
    Cas Lek Cesk; 2009; 148(7):296-302. PubMed ID: 19642294
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Whole-exome/genome sequencing and genomics.
    Grody WW; Thompson BH; Hudgins L
    Pediatrics; 2013 Dec; 132(Suppl 3):S211-5. PubMed ID: 24298129
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genome sequencing and assembly.
    Grabherr MG; Mauceli E; Ma LJ
    Methods Mol Biol; 2011; 722():1-9. PubMed ID: 21590409
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. [Cancer genome analysis through next-generation sequencing].
    Aburatani H
    Gan To Kagaku Ryoho; 2011 Jan; 38(1):1-6. PubMed ID: 21368453
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Representing genetic variation with synthetic DNA standards.
    Deveson IW; Chen WY; Wong T; Hardwick SA; Andersen SB; Nielsen LK; Mattick JS; Mercer TR
    Nat Methods; 2016 Sep; 13(9):784-91. PubMed ID: 27502217
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Sequencing genomes: from individuals to populations.
    Mir KU
    Brief Funct Genomic Proteomic; 2009 Sep; 8(5):367-78. PubMed ID: 19808932
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Single-molecule DNA sequencing technologies for future genomics research.
    Gupta PK
    Trends Biotechnol; 2008 Nov; 26(11):602-11. PubMed ID: 18722683
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The clinical implementation of whole genome sequencing: a conversation with seven scientific experts.
    Lerner-Ellis JP
    J Inherit Metab Dis; 2012 Jul; 35(4):689-93. PubMed ID: 22403015
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.