BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

165 related articles for article (PubMed ID: 23028300)

  • 21. Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models.
    Andrews TD; Whittle B; Field MA; Balakishnan B; Zhang Y; Shao Y; Cho V; Kirk M; Singh M; Xia Y; Hager J; Winslade S; Sjollema G; Beutler B; Enders A; Goodnow CC
    Open Biol; 2012 May; 2(5):120061. PubMed ID: 22724066
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Exome sequencing reveals the likely involvement of SOX10 in uveal melanoma.
    Das D; Kaur I; Ali MJ; Biswas NK; Das S; Kumar S; Honavar SG; Maitra A; Chakrabarti S; Majumder PP
    Optom Vis Sci; 2014 Jul; 91(7):e185-92. PubMed ID: 24927141
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Feature-based classifiers for somatic mutation detection in tumour-normal paired sequencing data.
    Ding J; Bashashati A; Roth A; Oloumi A; Tse K; Zeng T; Haffari G; Hirst M; Marra MA; Condon A; Aparicio S; Shah SP
    Bioinformatics; 2012 Jan; 28(2):167-75. PubMed ID: 22084253
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Evaluating somatic tumor mutation detection without matched normal samples.
    Teer JK; Zhang Y; Chen L; Welsh EA; Cress WD; Eschrich SA; Berglund AE
    Hum Genomics; 2017 Sep; 11(1):22. PubMed ID: 28870239
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Evaluation of KRAS, NRAS and BRAF hotspot mutations detection for patients with metastatic colorectal cancer using direct DNA pipetting in a fully-automated platform and Next-Generation Sequencing for laboratory workflow optimisation.
    Gilson P; Franczak C; Dubouis L; Husson M; Rouyer M; Demange J; Perceau M; Leroux A; Merlin JL; Harlé A
    PLoS One; 2019; 14(7):e0219204. PubMed ID: 31265477
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Exome sequence read depth methods for identifying copy number changes.
    Kadalayil L; Rafiq S; Rose-Zerilli MJ; Pengelly RJ; Parker H; Oscier D; Strefford JC; Tapper WJ; Gibson J; Ennis S; Collins A
    Brief Bioinform; 2015 May; 16(3):380-92. PubMed ID: 25169955
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Comprehensive analysis to improve the validation rate for single nucleotide variants detected by next-generation sequencing.
    Park MH; Rhee H; Park JH; Woo HM; Choi BO; Kim BY; Chung KW; Cho YB; Kim HJ; Jung JW; Koo SK
    PLoS One; 2014; 9(1):e86664. PubMed ID: 24489763
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A cancer cell-line titration series for evaluating somatic classification.
    Denroche RE; Mullen L; Timms L; Beck T; Yung CK; Stein L; McPherson JD; Brown AM
    BMC Res Notes; 2015 Dec; 8():823. PubMed ID: 26708082
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Amplicon-Based NGS Panels for Actionable Cancer Target Identification in Follicular Cell-Derived Thyroid Neoplasia.
    Madsen MB; Kiss K; Cilius Nielsen F; Bennedbæk FN; Rossing M
    Front Endocrinol (Lausanne); 2020; 11():146. PubMed ID: 32265839
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Challenges in next generation sequencing analysis of somatic mutations in transplant patients.
    Chen H; Luthra R; Patel KP; Routbort M; Rashid A; Roy-Chowdhuri S; Lazar A; Broaddus R; Manekia J; Singh RR; Yemelyanova A
    Cancer Genet; 2018 Oct; 226-227():17-22. PubMed ID: 30005850
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Implementation of next generation sequencing technology for somatic mutation detection in routine laboratory practice.
    Giardina T; Robinson C; Grieu-Iacopetta F; Millward M; Iacopetta B; Spagnolo D; Amanuel B
    Pathology; 2018 Jun; 50(4):389-401. PubMed ID: 29752127
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Profiling cancer gene mutations in clinical formalin-fixed, paraffin-embedded colorectal tumor specimens using targeted next-generation sequencing.
    Zhang L; Chen L; Sah S; Latham GJ; Patel R; Song Q; Koeppen H; Tam R; Schleifman E; Mashhedi H; Chalasani S; Fu L; Sumiyoshi T; Raja R; Forrest W; Hampton GM; Lackner MR; Hegde P; Jia S
    Oncologist; 2014 Apr; 19(4):336-43. PubMed ID: 24664487
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Next-Generation Genotyping by Digital PCR to Detect and Quantify the BRAF V600E Mutation in Melanoma Biopsies.
    Lamy PJ; Castan F; Lozano N; Montélion C; Audran P; Bibeau F; Roques S; Montels F; Laberenne AC
    J Mol Diagn; 2015 Jul; 17(4):366-73. PubMed ID: 25952101
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Discovery of potential causative mutations in human coding and noncoding genome with the interactive software BasePlayer.
    Katainen R; Donner I; Cajuso T; Kaasinen E; Palin K; Mäkinen V; Aaltonen LA; Pitkänen E
    Nat Protoc; 2018 Nov; 13(11):2580-2600. PubMed ID: 30323186
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Whole-exome sequencing studies of nonfunctioning pituitary adenomas.
    Newey PJ; Nesbit MA; Rimmer AJ; Head RA; Gorvin CM; Attar M; Gregory L; Wass JA; Buck D; Karavitaki N; Grossman AB; McVean G; Ansorge O; Thakker RV
    J Clin Endocrinol Metab; 2013 Apr; 98(4):E796-800. PubMed ID: 23450047
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma.
    Kloss-Brandstätter A; Weissensteiner H; Erhart G; Schäfer G; Forer L; Schönherr S; Pacher D; Seifarth C; Stöckl A; Fendt L; Sottsas I; Klocker H; Huck CW; Rasse M; Kronenberg F; Kloss FR
    PLoS One; 2015; 10(8):e0135643. PubMed ID: 26262956
    [TBL] [Abstract][Full Text] [Related]  

  • 38. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing.
    Koboldt DC; Zhang Q; Larson DE; Shen D; McLellan MD; Lin L; Miller CA; Mardis ER; Ding L; Wilson RK
    Genome Res; 2012 Mar; 22(3):568-76. PubMed ID: 22300766
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of somatic mutations in parathyroid tumors using whole-exome sequencing.
    Cromer MK; Starker LF; Choi M; Udelsman R; Nelson-Williams C; Lifton RP; Carling T
    J Clin Endocrinol Metab; 2012 Sep; 97(9):E1774-81. PubMed ID: 22740705
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Detection of Somatic Mutations in Exome Sequencing of Tumor-only Samples.
    Hsu YC; Hsiao YT; Kao TY; Chang JG; Shieh GS
    Sci Rep; 2017 Nov; 7(1):15959. PubMed ID: 29162841
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.