BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

214 related articles for article (PubMed ID: 21920051)

  • 1. Exome sequencing: the expert view.
    Biesecker LG; Shianna KV; Mullikin JC
    Genome Biol; 2011 Sep; 12(9):128. PubMed ID: 21920051
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Next-generation human genetics.
    Shendure J
    Genome Biol; 2011 Sep; 12(9):408. PubMed ID: 21920048
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Computational and statistical approaches to analyzing variants identified by exome sequencing.
    Stitziel NO; Kiezun A; Sunyaev S
    Genome Biol; 2011 Sep; 12(9):227. PubMed ID: 21920052
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genomics. Researchers to explore promise, risks of sequencing newborns' DNA.
    Kaiser J
    Science; 2013 Sep; 341(6151):1163. PubMed ID: 24030994
    [No Abstract]   [Full Text] [Related]  

  • 5. Genetic screening: birthright or earned with age?
    Mollison L; Berg JS
    Expert Rev Mol Diagn; 2017 Aug; 17(8):735-738. PubMed ID: 28641021
    [No Abstract]   [Full Text] [Related]  

  • 6. Unlocking Mendelian disease using exome sequencing.
    Gilissen C; Hoischen A; Brunner HG; Veltman JA
    Genome Biol; 2011 Sep; 12(9):228. PubMed ID: 21920049
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The exome factor.
    Stower H
    Genome Biol; 2011 Sep; 12(9):407. PubMed ID: 21920053
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinically Responsive Genomic Analysis Pipelines: Elements to Improve Detection Rate and Efficiency.
    Sundercombe SL; Berbic M; Evans CA; Cliffe C; Elakis G; Temple SEL; Selvanathan A; Ewans L; Quayum N; Nixon CY; Dias KR; Lang S; Richards A; Goh S; Wilson M; Mowat D; Sachdev R; Sandaradura S; Walsh M; Farrar MA; Walsh R; Fletcher J; Kirk EP; Teunisse GM; Schofield D; Buckley MF; Zhu Y; Roscioli T
    J Mol Diagn; 2021 Jul; 23(7):894-905. PubMed ID: 33962052
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diagnostic clinical genome and exome sequencing.
    Biesecker LG; Green RC
    N Engl J Med; 2014 Jun; 370(25):2418-25. PubMed ID: 24941179
    [No Abstract]   [Full Text] [Related]  

  • 10. Controversy and debate on clinical genomics sequencing-paper 2: clinical genome-wide sequencing: don't throw out the baby with the bathwater!
    Adam S; Friedman JM
    J Clin Epidemiol; 2017 Dec; 92():7-10. PubMed ID: 28916491
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Reanalysis of Clinical Exome Sequencing Data.
    Liu P; Meng L; Normand EA; Xia F; Song X; Ghazi A; Rosenfeld J; Magoulas PL; Braxton A; Ward P; Dai H; Yuan B; Bi W; Xiao R; Wang X; Chiang T; Vetrini F; He W; Cheng H; Dong J; Gijavanekar C; Benke PJ; Bernstein JA; Eble T; Eroglu Y; Erwin D; Escobar L; Gibson JB; Gripp K; Kleppe S; Koenig MK; Lewis AM; Natowicz M; Mancias P; Minor L; Scaglia F; Schaaf CP; Streff H; Vernon H; Uhles CL; Zackai EH; Wu N; Sutton VR; Beaudet AL; Muzny D; Gibbs RA; Posey JE; Lalani S; Shaw C; Eng CM; Lupski JR; Yang Y
    N Engl J Med; 2019 Jun; 380(25):2478-2480. PubMed ID: 31216405
    [No Abstract]   [Full Text] [Related]  

  • 12. Development and Validation of Clinical Whole-Exome and Whole-Genome Sequencing for Detection of Germline Variants in Inherited Disease.
    Hegde M; Santani A; Mao R; Ferreira-Gonzalez A; Weck KE; Voelkerding KV
    Arch Pathol Lab Med; 2017 Jun; 141(6):798-805. PubMed ID: 28362156
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exome sequencing a review of new strategies for rare genomic disease research.
    Brown TL; Meloche TM
    Genomics; 2016 Oct; 108(3-4):109-114. PubMed ID: 27387609
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Taking genomes personally.
    Lehrman S
    Sci Am; 2008 May; 298(5):20, 22. PubMed ID: 18444317
    [No Abstract]   [Full Text] [Related]  

  • 15. Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders.
    Rabbani B; Mahdieh N; Hosomichi K; Nakaoka H; Inoue I
    J Hum Genet; 2012 Oct; 57(10):621-32. PubMed ID: 22832387
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Next generation sequencing: the technology we need in pediatric laboratories?
    Couderc R; Jonard L; Louha M
    Clin Biochem; 2011 May; 44(7):514-515. PubMed ID: 22036354
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
    LaDuca H; Farwell KD; Vuong H; Lu HM; Mu W; Shahmirzadi L; Tang S; Chen J; Bhide S; Chao EC
    PLoS One; 2017; 12(2):e0170843. PubMed ID: 28152038
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Technology: Read the instructions.
    Scott AR
    Nature; 2016 Sep; 537(7619):S54-6. PubMed ID: 27602740
    [No Abstract]   [Full Text] [Related]  

  • 20. Genetic diagnosis through whole-exome sequencing.
    Jacob HJ
    N Engl J Med; 2014 Mar; 370(11):1069. PubMed ID: 24627900
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 11.