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 *

230 related articles for article (PubMed ID: 20127974)

  • 41. Next-generation sequencing methods: impact of sequencing accuracy on SNP discovery.
    Chan EY
    Methods Mol Biol; 2009; 578():95-111. PubMed ID: 19768588
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Clinical genomics: from a truly personal genome viewpoint.
    Lupski JR
    Hum Genet; 2016 Jun; 135(6):591-601. PubMed ID: 27221143
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Next-generation DNA sequencing methods.
    Mardis ER
    Annu Rev Genomics Hum Genet; 2008; 9():387-402. PubMed ID: 18576944
    [TBL] [Abstract][Full Text] [Related]  

  • 44. A decade's perspective on DNA sequencing technology.
    Mardis ER
    Nature; 2011 Feb; 470(7333):198-203. PubMed ID: 21307932
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Whole exome and whole genome sequencing.
    Bick D; Dimmock D
    Curr Opin Pediatr; 2011 Dec; 23(6):594-600. PubMed ID: 21881504
    [TBL] [Abstract][Full Text] [Related]  

  • 46. What can exome sequencing do for you?
    Majewski J; Schwartzentruber J; Lalonde E; Montpetit A; Jabado N
    J Med Genet; 2011 Sep; 48(9):580-9. PubMed ID: 21730106
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Next-generation sequencing: ready for the clinics?
    Desai AN; Jere A
    Clin Genet; 2012 Jun; 81(6):503-10. PubMed ID: 22375550
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Significance of functional disease-causal/susceptible variants identified by whole-genome analyses for the understanding of human diseases.
    Hitomi Y; Tokunaga K
    Proc Jpn Acad Ser B Phys Biol Sci; 2017; 93(9):657-676. PubMed ID: 29129848
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Next-generation sequencing technologies for DNA methylation analyses in cancer genomics.
    Boerno ST; Grimm C; Lehrach H; Schweiger MR
    Epigenomics; 2010 Apr; 2(2):199-207. PubMed ID: 22121870
    [TBL] [Abstract][Full Text] [Related]  

  • 50. A glimpse into past, present, and future DNA sequencing.
    Morey M; Fernández-Marmiesse A; Castiñeiras D; Fraga JM; Couce ML; Cocho JA
    Mol Genet Metab; 2013; 110(1-2):3-24. PubMed ID: 23742747
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells.
    Peters BA; Kermani BG; Sparks AB; Alferov O; Hong P; Alexeev A; Jiang Y; Dahl F; Tang YT; Haas J; Robasky K; Zaranek AW; Lee JH; Ball MP; Peterson JE; Perazich H; Yeung G; Liu J; Chen L; Kennemer MI; Pothuraju K; Konvicka K; Tsoupko-Sitnikov M; Pant KP; Ebert JC; Nilsen GB; Baccash J; Halpern AL; Church GM; Drmanac R
    Nature; 2012 Jul; 487(7406):190-5. PubMed ID: 22785314
    [TBL] [Abstract][Full Text] [Related]  

  • 52. DNA fingerprinting, DNA barcoding, and next generation sequencing technology in plants.
    Sucher NJ; Hennell JR; Carles MC
    Methods Mol Biol; 2012; 862():13-22. PubMed ID: 22419485
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Bacterial genome sequencing.
    Tettelin H; Feldblyum T
    Methods Mol Biol; 2009; 551():231-47. PubMed ID: 19521879
    [TBL] [Abstract][Full Text] [Related]  

  • 54. ABCs of genomics.
    Bohlander SK
    Hematology Am Soc Hematol Educ Program; 2013; 2013():316-23. PubMed ID: 24319198
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Microarray and next-generation sequencing to analyse gastric cancer.
    Dang Y; Wang YC; Huang QJ
    Asian Pac J Cancer Prev; 2014; 15(19):8033-9. PubMed ID: 25338980
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Genomics of AML: clinical applications of next-generation sequencing.
    Welch JS; Link DC
    Hematology Am Soc Hematol Educ Program; 2011; 2011():30-5. PubMed ID: 22160009
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Next generation sequencing technologies (NGST) -- development and applications].
    Mihály Z; Gyorffy B
    Orv Hetil; 2011 Jan; 152(2):55-62. PubMed ID: 21177232
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Future Promises and Concerns of Ubiquitous Next-Generation Sequencing.
    McCombie WR; McPherson JD
    Cold Spring Harb Perspect Med; 2019 Sep; 9(9):. PubMed ID: 30478095
    [TBL] [Abstract][Full Text] [Related]  

  • 59. HySA: a Hybrid Structural variant Assembly approach using next-generation and single-molecule sequencing technologies.
    Fan X; Chaisson M; Nakhleh L; Chen K
    Genome Res; 2017 May; 27(5):793-800. PubMed ID: 28104618
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Personal genomes: Standard and pores.
    Sanderson K
    Nature; 2008 Nov; 456(7218):23-5. PubMed ID: 18987710
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.