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 *

127 related articles for article (PubMed ID: 26451822)

  • 1. Inferring Sequential Order of Somatic Mutations during Tumorgenesis based on Markov Chain Model.
    Kang H; Cho KH; Zhang XD; Zeng T; Chen L
    IEEE/ACM Trans Comput Biol Bioinform; 2015; 12(5):1094-103. PubMed ID: 26451822
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A novel framework for analyzing somatic copy number aberrations and tumor subclones for paired heterogeneous tumor samples.
    Xia H; Li A; Yu Z; Liu X; Feng H
    Biomed Mater Eng; 2015; 26 Suppl 1():S1845-53. PubMed ID: 26405956
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Deciphering oncogenic drivers: from single genes to integrated pathways.
    Chen J; Sun M; Shen B
    Brief Bioinform; 2015 May; 16(3):413-28. PubMed ID: 25378434
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High-throughput detection of clinically relevant mutations in archived tumor samples by multiplexed PCR and next-generation sequencing.
    Bourgon R; Lu S; Yan Y; Lackner MR; Wang W; Weigman V; Wang D; Guan Y; Ryner L; Koeppen H; Patel R; Hampton GM; Amler LC; Wang Y
    Clin Cancer Res; 2014 Apr; 20(8):2080-91. PubMed ID: 24573554
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A probabilistic method for leveraging functional annotations to enhance estimation of the temporal order of pathway mutations during carcinogenesis.
    Wang M; Yu T; Liu J; Chen L; Stromberg AJ; Villano JL; Arnold SM; Liu C; Wang C
    BMC Bioinformatics; 2019 Dec; 20(1):620. PubMed ID: 31791231
    [TBL] [Abstract][Full Text] [Related]  

  • 6. SubClonal Hierarchy Inference from Somatic Mutations: Automatic Reconstruction of Cancer Evolutionary Trees from Multi-region Next Generation Sequencing.
    Niknafs N; Beleva-Guthrie V; Naiman DQ; Karchin R
    PLoS Comput Biol; 2015 Oct; 11(10):e1004416. PubMed ID: 26436540
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Fundamentals of pyrosequencing.
    Harrington CT; Lin EI; Olson MT; Eshleman JR
    Arch Pathol Lab Med; 2013 Sep; 137(9):1296-303. PubMed ID: 23991743
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Whole-exome sequencing reveals recurrent somatic mutation networks in cancer.
    Liu X; Wang J; Chen L
    Cancer Lett; 2013 Nov; 340(2):270-6. PubMed ID: 23153794
    [TBL] [Abstract][Full Text] [Related]  

  • 9. LNDriver: identifying driver genes by integrating mutation and expression data based on gene-gene interaction network.
    Wei PJ; Zhang D; Xia J; Zheng CH
    BMC Bioinformatics; 2016 Dec; 17(Suppl 17):467. PubMed ID: 28155630
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Role of high-throughput sequencing in oncology].
    Rodrigues MJ; Gomez-Roca C
    Bull Cancer; 2013 Mar; 100(3):295-301. PubMed ID: 23501647
    [TBL] [Abstract][Full Text] [Related]  

  • 11. High frequency of deletion mutations in p53 gene from squamous cell lung cancer patients in Taiwan.
    Wang YC; Chen CY; Chen SK; Cherng SH; Ho WL; Lee H
    Cancer Res; 1998 Jan; 58(2):328-33. PubMed ID: 9443413
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A novel method to quantify base substitution mutations at the 10
    Yamashita S; Iida N; Takeshima H; Hattori N; Maeda M; Kishino T; Nagano R; Shimazu T; Tsugane S; Ushijima T
    Cancer Lett; 2017 Sep; 403():152-158. PubMed ID: 28642169
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Signs of positive selection of somatic mutations in human cancers detected by EST sequence analysis.
    Babenko VN; Basu MK; Kondrashov FA; Rogozin IB; Koonin EV
    BMC Cancer; 2006 Feb; 6():36. PubMed ID: 16469093
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Rapid targeted somatic mutation analysis of solid tumors in routine clinical diagnostics.
    Magliacane G; Grassini G; Bartocci P; Francaviglia I; Dal Cin E; Barbieri G; Arrigoni G; Pecciarini L; Doglioni C; Cangi MG
    Oncotarget; 2015 Oct; 6(31):30592-603. PubMed ID: 26435479
    [TBL] [Abstract][Full Text] [Related]  

  • 15. mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing.
    Li J; Jiang Y; Wang T; Chen H; Xie Q; Shao Q; Ran X; Xia K; Sun ZS; Wu J
    J Med Genet; 2015 Apr; 52(4):275-81. PubMed ID: 25596308
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Next generation sequencing technologies in cancer diagnostics and therapeutics: A mini review.
    Li W; Zhao K; Kirberger M; Liao W; Yan Y
    Cell Mol Biol (Noisy-le-grand); 2015 Oct; 61(5):91-102. PubMed ID: 26522064
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Local sequence assembly reveals a high-resolution profile of somatic structural variations in 97 cancer genomes.
    Zhuang J; Weng Z
    Nucleic Acids Res; 2015 Sep; 43(17):8146-56. PubMed ID: 26283183
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Direct quantification of in vivo mutagenesis and carcinogenesis using duplex sequencing.
    Valentine CC; Young RR; Fielden MR; Kulkarni R; Williams LN; Li T; Minocherhomji S; Salk JJ
    Proc Natl Acad Sci U S A; 2020 Dec; 117(52):33414-33425. PubMed ID: 33318186
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Simple Model-Based Approach to Inferring and Visualizing Cancer Mutation Signatures.
    Shiraishi Y; Tremmel G; Miyano S; Stephens M
    PLoS Genet; 2015 Dec; 11(12):e1005657. PubMed ID: 26630308
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High-throughput scanning of breast tumor surgical specimens for low-level mutations.
    Wang F; Kaur M; Liu WH; Zhu P; Li J; Wang L; Makrigiorgos GM
    Clin Chem Lab Med; 2005; 43(8):810-6. PubMed ID: 16201889
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.