BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

271 related articles for article (PubMed ID: 24297533)

  • 1. Detecting statistical interaction between somatic mutational events and germline variation from next-generation sequence data.
    Hu H; Huff CD
    Pac Symp Biocomput; 2014; ():51-62. PubMed ID: 24297533
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Exome-wide analysis of bi-allelic alterations identifies a Lynch phenotype in The Cancer Genome Atlas.
    Buckley AR; Ideker T; Carter H; Harismendy O; Schork NJ
    Genome Med; 2018 Sep; 10(1):69. PubMed ID: 30217226
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A computational approach to distinguish somatic vs. germline origin of genomic alterations from deep sequencing of cancer specimens without a matched normal.
    Sun JX; He Y; Sanford E; Montesion M; Frampton GM; Vignot S; Soria JC; Ross JS; Miller VA; Stephens PJ; Lipson D; Yelensky R
    PLoS Comput Biol; 2018 Feb; 14(2):e1005965. PubMed ID: 29415044
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Germline and somatic mutations in patients with multiple primary melanomas: a next generation sequencing study.
    Casula M; Paliogiannis P; Ayala F; De Giorgi V; Stanganelli I; Mandalà M; Colombino M; Manca A; Sini MC; Caracò C; Ascierto PA; Satta RR; ; Lissia A; Cossu A; Palmieri G;
    BMC Cancer; 2019 Aug; 19(1):772. PubMed ID: 31382929
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A method to reduce ancestry related germline false positives in tumor only somatic variant calling.
    Halperin RF; Carpten JD; Manojlovic Z; Aldrich J; Keats J; Byron S; Liang WS; Russell M; Enriquez D; Claasen A; Cherni I; Awuah B; Oppong J; Wicha MS; Newman LA; Jaigge E; Kim S; Craig DW
    BMC Med Genomics; 2017 Oct; 10(1):61. PubMed ID: 29052513
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tumor sequencing is useful to refine the analysis of germline variants in unexplained high-risk breast cancer families.
    Van Marcke C; Helaers R; De Leener A; Merhi A; Schoonjans CA; Ambroise J; Galant C; Delrée P; Rothé F; Bar I; Khoury E; Brouillard P; Canon JL; Vuylsteke P; Machiels JP; Berlière M; Limaye N; Vikkula M; Duhoux FP
    Breast Cancer Res; 2020 Apr; 22(1):36. PubMed ID: 32295625
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Germline Mutations for Novel Candidate Predisposition Genes in Sporadic Schwannomatosis.
    Min BJ; Kang YK; Chung YG; Seo ME; Chang KB; Joo MW
    Clin Orthop Relat Res; 2020 Nov; 478(11):2442-2450. PubMed ID: 32281771
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Strelka2: fast and accurate calling of germline and somatic variants.
    Kim S; Scheffler K; Halpern AL; Bekritsky MA; Noh E; Källberg M; Chen X; Kim Y; Beyter D; Krusche P; Saunders CT
    Nat Methods; 2018 Aug; 15(8):591-594. PubMed ID: 30013048
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Origins and characterization of variants shared between databases of somatic and germline human mutations.
    Meyerson W; Leisman J; Navarro FCP; Gerstein M
    BMC Bioinformatics; 2020 Jun; 21(1):227. PubMed ID: 32498674
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Germline and Somatic Genetic Variants in the p53 Pathway Interact to Affect Cancer Risk, Progression, and Drug Response.
    Zhang P; Kitchen-Smith I; Xiong L; Stracquadanio G; Brown K; Richter PH; Wallace MD; Bond E; Sahgal N; Moore S; Nornes S; De Val S; Surakhy M; Sims D; Wang X; Bell DA; Zeron-Medina J; Jiang Y; Ryan AJ; Selfe JL; Shipley J; Kar S; Pharoah PD; Loveday C; Jansen R; Grochola LF; Palles C; Protheroe A; Millar V; Ebner DV; Pagadala M; Blagden SP; Maughan TS; Domingo E; Tomlinson I; Turnbull C; Carter H; Bond GL
    Cancer Res; 2021 Apr; 81(7):1667-1680. PubMed ID: 33558336
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Germline Variants Impact Somatic Events during Tumorigenesis.
    Ramroop JR; Gerber MM; Toland AE
    Trends Genet; 2019 Jul; 35(7):515-526. PubMed ID: 31128889
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes.
    Walsh MF; Ritter DI; Kesserwan C; Sonkin D; Chakravarty D; Chao E; Ghosh R; Kemel Y; Wu G; Lee K; Kulkarni S; Hedges D; Mandelker D; Ceyhan-Birsoy O; Luo M; Drazer M; Zhang L; Offit K; Plon SE
    Hum Mutat; 2018 Nov; 39(11):1542-1552. PubMed ID: 30311369
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Multiethnic Germline-Somatic Association Database Deciphers Multilayered and Interconnected Genetic Mutations in Cancer.
    Xin J; Mo Z; Chai R; Hua W; Wang J
    Cancer Res; 2024 Feb; 84(3):364-371. PubMed ID: 38016109
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Germline genetic variants were interactively associated with somatic alterations in gastric cancer.
    Zhang X; Wang Y; Tian T; Zhou G; Jin G
    Cancer Med; 2018 Aug; 7(8):3912-3920. PubMed ID: 29923336
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detection of somatic BRCA1/2 mutations in ovarian cancer - next-generation sequencing analysis of 100 cases.
    Koczkowska M; Zuk M; Gorczynski A; Ratajska M; Lewandowska M; Biernat W; Limon J; Wasag B
    Cancer Med; 2016 Jul; 5(7):1640-6. PubMed ID: 27167707
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing.
    Altmüller J; Haenisch B; Kawalia A; Menzen M; Nöthen MM; Fier H; Molderings GJ
    Immunogenetics; 2017 Jun; 69(6):359-369. PubMed ID: 28386644
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Germline Variants in Targeted Tumor Sequencing Using Matched Normal DNA.
    Schrader KA; Cheng DT; Joseph V; Prasad M; Walsh M; Zehir A; Ni A; Thomas T; Benayed R; Ashraf A; Lincoln A; Arcila M; Stadler Z; Solit D; Hyman DM; Zhang L; Klimstra D; Ladanyi M; Offit K; Berger M; Robson M
    JAMA Oncol; 2016 Jan; 2(1):104-11. PubMed ID: 26556299
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association between germline variants and somatic mutations in colorectal cancer.
    Barfield R; Qu C; Steinfelder RS; Zeng C; Harrison TA; Brezina S; Buchanan DD; Campbell PT; Casey G; Gallinger S; Giannakis M; Gruber SB; Gsur A; Hsu L; Huyghe JR; Moreno V; Newcomb PA; Ogino S; Phipps AI; Slattery ML; Thibodeau SN; Trinh QM; Toland AE; Hudson TJ; Sun W; Zaidi SH; Peters U
    Sci Rep; 2022 Jun; 12(1):10207. PubMed ID: 35715570
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Somatic mutation panels: Time to clear their names.
    Trottier AM; Cavalcante de Andrade Silva M; Li Z; Godley LA
    Cancer Genet; 2019 Jun; 235-236():84-92. PubMed ID: 31101556
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Haplotype-resolved germline and somatic alterations in renal medullary carcinomas.
    Tan KT; Kim H; Carrot-Zhang J; Zhang Y; Kim WJ; Kugener G; Wala JA; Howard TP; Chi YY; Beroukhim R; Li H; Ha G; Alper SL; Perlman EJ; Mullen EA; Hahn WC; Meyerson M; Hong AL
    Genome Med; 2021 Jul; 13(1):114. PubMed ID: 34261517
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.