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 *

186 related articles for article (PubMed ID: 38183204)

  • 21. A framework for organizing cancer-related variations from existing databases, publications and NGS data using a High-performance Integrated Virtual Environment (HIVE).
    Wu TJ; Shamsaddini A; Pan Y; Smith K; Crichton DJ; Simonyan V; Mazumder R
    Database (Oxford); 2014; 2014():bau022. PubMed ID: 24667251
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The clinical trial landscape in oncology and connectivity of somatic mutational profiles to targeted therapies.
    Patterson SE; Liu R; Statz CM; Durkin D; Lakshminarayana A; Mockus SM
    Hum Genomics; 2016 Jan; 10():4. PubMed ID: 26772741
    [TBL] [Abstract][Full Text] [Related]  

  • 23. COSMIC Cancer Gene Census 3D database: understanding the impacts of mutations on cancer targets.
    Alsulami AF; Torres PHM; Moghul I; Arif SM; Chaplin AK; Vedithi SC; Blundell TL
    Brief Bioinform; 2021 Nov; 22(6):. PubMed ID: 34137435
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Data resources for the identification and interpretation of actionable mutations by clinicians.
    Prawira A; Pugh TJ; Stockley TL; Siu LL
    Ann Oncol; 2017 May; 28(5):946-957. PubMed ID: 28327901
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A harmonized meta-knowledgebase of clinical interpretations of somatic genomic variants in cancer.
    Wagner AH; Walsh B; Mayfield G; Tamborero D; Sonkin D; Krysiak K; Deu-Pons J; Duren RP; Gao J; McMurry J; Patterson S; Del Vecchio Fitz C; Pitel BA; Sezerman OU; Ellrott K; Warner JL; Rieke DT; Aittokallio T; Cerami E; Ritter DI; Schriml LM; Freimuth RR; Haendel M; Raca G; Madhavan S; Baudis M; Beckmann JS; Dienstmann R; Chakravarty D; Li XS; Mockus S; Elemento O; Schultz N; Lopez-Bigas N; Lawler M; Goecks J; Griffith M; Griffith OL; Margolin AA;
    Nat Genet; 2020 Apr; 52(4):448-457. PubMed ID: 32246132
    [TBL] [Abstract][Full Text] [Related]  

  • 26. CCG: an integrative resource of cancer protein-coding genes and long noncoding RNAs.
    Liu M; Yang YT; Xu G; Tan C; Lu ZJ
    Discov Med; 2016 Dec; 22(123):351-359. PubMed ID: 28147217
    [TBL] [Abstract][Full Text] [Related]  

  • 27. DAVID Knowledgebase: a gene-centered database integrating heterogeneous gene annotation resources to facilitate high-throughput gene functional analysis.
    Sherman BT; Huang da W; Tan Q; Guo Y; Bour S; Liu D; Stephens R; Baseler MW; Lane HC; Lempicki RA
    BMC Bioinformatics; 2007 Nov; 8():426. PubMed ID: 17980028
    [TBL] [Abstract][Full Text] [Related]  

  • 28. VarStack: a web tool for data retrieval to interpret somatic variants in cancer.
    Howard M; Kane B; Lepry M; Stey P; Ragavendran A; Gamsiz Uzun ED
    Database (Oxford); 2020 Nov; 2020():. PubMed ID: 33247936
    [TBL] [Abstract][Full Text] [Related]  

  • 29. MosaicBase: A Knowledgebase of Postzygotic Mosaic Variants in Noncancer Disease-related and Healthy Human Individuals.
    Yang X; Yang C; Zheng X; Xiong L; Tao Y; Wang M; Ye AY; Wu Q; Dou Y; Luo J; Wei L; Huang AY
    Genomics Proteomics Bioinformatics; 2020 Apr; 18(2):140-149. PubMed ID: 32911083
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The Mutational Signature Comprehensive Analysis Toolkit (musicatk) for the Discovery, Prediction, and Exploration of Mutational Signatures.
    Chevalier A; Yang S; Khurshid Z; Sahelijo N; Tong T; Huggins JH; Yajima M; Campbell JD
    Cancer Res; 2021 Dec; 81(23):5813-5817. PubMed ID: 34625425
    [TBL] [Abstract][Full Text] [Related]  

  • 31. cancercelllines.org-a novel resource for genomic variants in cancer cell lines.
    Paloots R; Baudis M
    Database (Oxford); 2024 Apr; 2024():. PubMed ID: 38687868
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Genomics of Drug Sensitivity in Cancer (GDSC): a resource for therapeutic biomarker discovery in cancer cells.
    Yang W; Soares J; Greninger P; Edelman EJ; Lightfoot H; Forbes S; Bindal N; Beare D; Smith JA; Thompson IR; Ramaswamy S; Futreal PA; Haber DA; Stratton MR; Benes C; McDermott U; Garnett MJ
    Nucleic Acids Res; 2013 Jan; 41(Database issue):D955-61. PubMed ID: 23180760
    [TBL] [Abstract][Full Text] [Related]  

  • 34. vcf2fhir: a utility to convert VCF files into HL7 FHIR format for genomics-EHR integration.
    Dolin RH; Gothi SR; Boxwala A; Heale BSE; Husami A; Jones J; Khangar H; Londhe S; Naeymi-Rad F; Rao S; Rapchak B; Shalaby J; Suraj V; Xie N; Chamala S; Alterovitz G
    BMC Bioinformatics; 2021 Mar; 22(1):104. PubMed ID: 33653260
    [TBL] [Abstract][Full Text] [Related]  

  • 35. IDENTIFY CANCER DRIVER GENES THROUGH SHARED MENDELIAN DISEASE PATHOGENIC VARIANTS AND CANCER SOMATIC MUTATIONS.
    Ma M; Wang C; Glicksberg BS; Schadt EE; Li SD; Chen R
    Pac Symp Biocomput; 2017; 22():473-484. PubMed ID: 27896999
    [TBL] [Abstract][Full Text] [Related]  

  • 36. tmVar 2.0: integrating genomic variant information from literature with dbSNP and ClinVar for precision medicine.
    Wei CH; Phan L; Feltz J; Maiti R; Hefferon T; Lu Z
    Bioinformatics; 2018 Jan; 34(1):80-87. PubMed ID: 28968638
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The DisGeNET knowledge platform for disease genomics: 2019 update.
    Piñero J; Ramírez-Anguita JM; Saüch-Pitarch J; Ronzano F; Centeno E; Sanz F; Furlong LI
    Nucleic Acids Res; 2020 Jan; 48(D1):D845-D855. PubMed ID: 31680165
    [TBL] [Abstract][Full Text] [Related]  

  • 38. canSAR: update to the cancer translational research and drug discovery knowledgebase.
    Mitsopoulos C; Di Micco P; Fernandez EV; Dolciami D; Holt E; Mica IL; Coker EA; Tym JE; Campbell J; Che KH; Ozer B; Kannas C; Antolin AA; Workman P; Al-Lazikani B
    Nucleic Acids Res; 2021 Jan; 49(D1):D1074-D1082. PubMed ID: 33219674
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The COSMIC Cancer Gene Census: describing genetic dysfunction across all human cancers.
    Sondka Z; Bamford S; Cole CG; Ward SA; Dunham I; Forbes SA
    Nat Rev Cancer; 2018 Nov; 18(11):696-705. PubMed ID: 30293088
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Unravelling the instability of mutational signatures extraction
    Pancotti C; Rollo C; Birolo G; Benevenuta S; Fariselli P; Sanavia T
    Front Genet; 2022; 13():1049501. PubMed ID: 36685831
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.