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 *

463 related articles for article (PubMed ID: 24870132)

  • 1. Studying cancer genomics through next-generation DNA sequencing and bioinformatics.
    Doyle MA; Li J; Doig K; Fellowes A; Wong SQ
    Methods Mol Biol; 2014; 1168():83-98. PubMed ID: 24870132
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Bioinformatics Data Analysis of Next-Generation Sequencing Data from Heterogeneous Tumor Samples.
    Landman SR; Hwang TH
    Methods Mol Biol; 2017; 1633():185-192. PubMed ID: 28735488
    [TBL] [Abstract][Full Text] [Related]  

  • 3. TumorNext: A comprehensive tumor profiling assay that incorporates high resolution copy number analysis and germline status to improve testing accuracy.
    Gray PN; Vuong H; Tsai P; Lu HM; Mu W; Hsuan V; Hoo J; Shah S; Uyeda L; Fox S; Patel H; Janicek M; Brown S; Dobrea L; Wagman L; Plimack E; Mehra R; Golemis EA; Bilusic M; Zibelman M; Elliott A
    Oncotarget; 2016 Oct; 7(42):68206-68228. PubMed ID: 27626691
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical application of amplicon-based next-generation sequencing in cancer.
    Chang F; Li MM
    Cancer Genet; 2013 Dec; 206(12):413-9. PubMed ID: 24332266
    [TBL] [Abstract][Full Text] [Related]  

  • 5. INDELseek: detection of complex insertions and deletions from next-generation sequencing data.
    Au CH; Leung AY; Kwong A; Chan TL; Ma ES
    BMC Genomics; 2017 Jan; 18(1):16. PubMed ID: 28056804
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Integrated next-generation sequencing analysis of whole exome and 409 cancer-related genes.
    Shimoda Y; Nagashima T; Urakami K; Tanabe T; Saito J; Naruoka A; Serizawa M; Mochizuki T; Ohshima K; Ohnami S; Ohnami S; Kusuhara M; Yamaguchi K
    Biomed Res; 2016; 37(6):367-379. PubMed ID: 28003584
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical Applications of Next-Generation Sequencing in Cancer Diagnosis.
    Sabour L; Sabour M; Ghorbian S
    Pathol Oncol Res; 2017 Apr; 23(2):225-234. PubMed ID: 27722982
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Computational analysis in cancer exome sequencing.
    Evans P; Kong Y; Krauthammer M
    Methods Mol Biol; 2014; 1176():219-27. PubMed ID: 25030931
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Whole cancer genome sequencing by next-generation methods.
    Ross JS; Cronin M
    Am J Clin Pathol; 2011 Oct; 136(4):527-39. PubMed ID: 21917674
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Understanding genomic alterations in cancer genomes using an integrative network approach.
    Wang E
    Cancer Lett; 2013 Nov; 340(2):261-9. PubMed ID: 23266571
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Comparative analysis of methods for identifying somatic copy number alterations from deep sequencing data.
    Alkodsi A; Louhimo R; Hautaniemi S
    Brief Bioinform; 2015 Mar; 16(2):242-54. PubMed ID: 24599115
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Tilling by sequencing.
    Tsai H; Ngo K; Lieberman M; Missirian V; Comai L
    Methods Mol Biol; 2015; 1284():359-80. PubMed ID: 25757782
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Application of high-throughput DNA sequencing in phytopathology.
    Studholme DJ; Glover RH; Boonham N
    Annu Rev Phytopathol; 2011; 49():87-105. PubMed ID: 21548771
    [TBL] [Abstract][Full Text] [Related]  

  • 14. ICO amplicon NGS data analysis: a Web tool for variant detection in common high-risk hereditary cancer genes analyzed by amplicon GS Junior next-generation sequencing.
    Lopez-Doriga A; Feliubadaló L; Menéndez M; Lopez-Doriga S; Morón-Duran FD; del Valle J; Tornero E; Montes E; Cuesta R; Campos O; Gómez C; Pineda M; González S; Moreno V; Capellá G; Lázaro C
    Hum Mutat; 2014 Mar; 35(3):271-7. PubMed ID: 24227591
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Computational methods for DNA copy-number analysis of tumors.
    Kendall J; Krasnitz A
    Methods Mol Biol; 2014; 1176():243-59. PubMed ID: 25030933
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Optimizing an ion semiconductor sequencing data analysis method to identify somatic mutations in the genomes of cancer cells in clinical tissue samples.
    Nagashima T; Shimoda Y; Tanabe T; Naruoka A; Saito J; Serizawa M; Ohshima K; Urakami K; Ohnami S; Ohnami S; Mochizuki T; Kusuhara M; Yamaguchi K
    Biomed Res; 2016; 37(6):359-366. PubMed ID: 28003583
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cancer omics: from regulatory networks to clinical outcomes.
    Tang B; Hsu PY; Huang TH; Jin VX
    Cancer Lett; 2013 Nov; 340(2):277-83. PubMed ID: 23201140
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Next generation mapping reveals novel large genomic rearrangements in prostate cancer.
    Jaratlerdsiri W; Chan EKF; Petersen DC; Yang C; Croucher PI; Bornman MSR; Sheth P; Hayes VM
    Oncotarget; 2017 Apr; 8(14):23588-23602. PubMed ID: 28423598
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. Whole-genome sequencing for comparative genomics and de novo genome assembly.
    Benjak A; Sala C; Hartkoorn RC
    Methods Mol Biol; 2015; 1285():1-16. PubMed ID: 25779307
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.