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 *

109 related articles for article (PubMed ID: 30285033)

  • 1. Need for Automated Interactive Genomic Interpretation and Ongoing Reanalysis.
    Sarmady M; Abou Tayoun A
    JAMA Pediatr; 2018 Dec; 172(12):1113-1114. PubMed ID: 30285033
    [No Abstract]   [Full Text] [Related]  

  • 2. The Next Generation of Molecular Pathology is Here: Validation of Next-Generation Sequencing Technology for Clinical Molecular Testing Across Multiple Different Disciplines.
    Weck KE
    Arch Pathol Lab Med; 2017 Jun; 141(6):749-750. PubMed ID: 28557596
    [No Abstract]   [Full Text] [Related]  

  • 3. Super-speedy sequencing puts genomic diagnosis in the fast lane.
    Eisenstein M
    Nature; 2024 Feb; 626(8000):915-917. PubMed ID: 38374432
    [No Abstract]   [Full Text] [Related]  

  • 4. Evolving health care through personal genomics.
    Rehm HL
    Nat Rev Genet; 2017 Apr; 18(4):259-267. PubMed ID: 28138143
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Next generation sequencing in hematolymphoid neoplasia.
    Kuo FC
    Semin Hematol; 2019 Jan; 56(1):2-6. PubMed ID: 30573040
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tearing down the walls: FDA approves next generation sequencing (NGS) assays for actionable cancer genomic aberrations.
    Allegretti M; Fabi A; Buglioni S; Martayan A; Conti L; Pescarmona E; Ciliberto G; Giacomini P
    J Exp Clin Cancer Res; 2018 Mar; 37(1):47. PubMed ID: 29506529
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Reanalysis of genomic data, how do we do it now and what if we automate it? A qualitative study.
    Fehlberg Z; Stark Z; Best S
    Eur J Hum Genet; 2024 May; 32(5):521-528. PubMed ID: 38212661
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical and Technical Aspects of Genomic Diagnostics for Precision Oncology.
    Sheikine Y; Kuo FC; Lindeman NI
    J Clin Oncol; 2017 Mar; 35(9):929-933. PubMed ID: 28297627
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluation for Genetic Disorders in the Absence of a Clinical Indication for Testing: Elective Genomic Testing.
    Lu JT; Ferber M; Hagenkord J; Levin E; South S; Kang HP; Strong KA; Bick DP
    J Mol Diagn; 2019 Jan; 21(1):3-12. PubMed ID: 30453057
    [TBL] [Abstract][Full Text] [Related]  

  • 10. How can mate-pair sequencing be utilized for cancer patients?
    Gao G; Smith DI
    Expert Rev Mol Diagn; 2017 Jan; 17(1):1-3. PubMed ID: 27830954
    [No Abstract]   [Full Text] [Related]  

  • 11. Insights of Acute Lymphoblastic Leukemia with Development of Genomic Investigation.
    Xu H; Shu Y
    Methods Mol Biol; 2018; 1754():387-413. PubMed ID: 29536454
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The DNA of a nation.
    Marx V
    Nature; 2015 Aug; 524(7566):503-5. PubMed ID: 26310768
    [No Abstract]   [Full Text] [Related]  

  • 13. [Novel high-throughput sequencing strategies in genetic diagnostics].
    Myllykangas S; Koskenvuo JW; Alastalo TP
    Duodecim; 2013; 129(2):141-8. PubMed ID: 23577577
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Application of advanced molecular technology in the diagnosis and management of genetic disorders in South Africa.
    Kotze M
    S Afr Med J; 2016 May; 106(6 Suppl 1):S114-8. PubMed ID: 27245544
    [TBL] [Abstract][Full Text] [Related]  

  • 15. AG-NGS: a powerful and user-friendly computing application for the semi-automated preparation of next-generation sequencing libraries using open liquid handling platforms.
    Callejas S; Álvarez R; Benguria A; Dopazo A
    Biotechniques; 2014 Jan; 56(1):28-35. PubMed ID: 24447136
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Safe sequencing depth to estimate the intra-host heterogeneity of viruses.
    Ren X; Jin Q
    Brief Funct Genomics; 2016 Jul; 15(4):275-7. PubMed ID: 26427942
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Controversy and debate on clinical genomics sequencing-paper 1: genomics is not exceptional: rigorous evaluations are necessary for clinical applications of genomic sequencing.
    Wilson BJ; Miller FA; Rousseau F
    J Clin Epidemiol; 2017 Dec; 92():4-6. PubMed ID: 28870871
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Diagnostic Single Gene Analyses Beyond Sanger.
    Najm J; Rath M; Schröder W; Felbor U
    Hamostaseologie; 2018 Aug; 38(3):158-165. PubMed ID: 30261521
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genomics for paediatricians: promises and pitfalls.
    Hammond CL; Willoughby JM; Parker MJ
    Arch Dis Child; 2018 Sep; 103(9):895-900. PubMed ID: 29574410
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A semi-automated system for analysis and storage of SNPs.
    Lehnert V; Holzwarth J; Ott M; Thompson A; Demmak S; Foernzler D
    Hum Mutat; 2001 Apr; 17(4):243-54. PubMed ID: 11295821
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.