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 *

95 related articles for article (PubMed ID: 33289511)

  • 1. AVIA 3.0: interactive portal for genomic variant and sample level analysis.
    Reardon HV; Che A; Luke BT; Ravichandran S; Collins JR; Mudunuri US
    Bioinformatics; 2021 Aug; 37(16):2467-2469. PubMed ID: 33289511
    [TBL] [Abstract][Full Text] [Related]  

  • 2. AVIA v2.0: annotation, visualization and impact analysis of genomic variants and genes.
    Vuong H; Che A; Ravichandran S; Luke BT; Collins JR; Mudunuri US
    Bioinformatics; 2015 Aug; 31(16):2748-50. PubMed ID: 25861966
    [TBL] [Abstract][Full Text] [Related]  

  • 3. AVIA: an interactive web-server for annotation, visualization and impact analysis of genomic variations.
    Vuong H; Stephens RM; Volfovsky N
    Bioinformatics; 2014 Apr; 30(7):1013-4. PubMed ID: 24215028
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial Disease Sequence Data Resource (MSeqDR): a global grass-roots consortium to facilitate deposition, curation, annotation, and integrated analysis of genomic data for the mitochondrial disease clinical and research communities.
    Falk MJ; Shen L; Gonzalez M; Leipzig J; Lott MT; Stassen AP; Diroma MA; Navarro-Gomez D; Yeske P; Bai R; Boles RG; Brilhante V; Ralph D; DaRe JT; Shelton R; Terry SF; Zhang Z; Copeland WC; van Oven M; Prokisch H; Wallace DC; Attimonelli M; Krotoski D; Zuchner S; Gai X; ; ; ; ; ;
    Mol Genet Metab; 2015 Mar; 114(3):388-96. PubMed ID: 25542617
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Gigwa v2-Extended and improved genotype investigator.
    Sempéré G; Pétel A; Rouard M; Frouin J; Hueber Y; De Bellis F; Larmande P
    Gigascience; 2019 May; 8(5):. PubMed ID: 31077313
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Clinical Genome and Ancestry Report: An interactive web application for prioritizing clinically implicated variants from genome sequencing data with ancestry composition.
    Lee IH; Negron JA; Hernandez-Ferrer C; Alvarez WJ; Mandl KD; Kong SW
    Hum Mutat; 2020 Feb; 41(2):387-396. PubMed ID: 31691385
    [TBL] [Abstract][Full Text] [Related]  

  • 7. VCF-Server: A web-based visualization tool for high-throughput variant data mining and management.
    Jiang J; Gu J; Zhao T; Lu H
    Mol Genet Genomic Med; 2019 Jul; 7(7):e00641. PubMed ID: 31127704
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genome analysis and knowledge-driven variant interpretation with TGex.
    Dahary D; Golan Y; Mazor Y; Zelig O; Barshir R; Twik M; Iny Stein T; Rosner G; Kariv R; Chen F; Zhang Q; Shen Y; Safran M; Lancet D; Fishilevich S
    BMC Med Genomics; 2019 Dec; 12(1):200. PubMed ID: 31888639
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Variant Ranker: a web-tool to rank genomic data according to functional significance.
    Alexander J; Mantzaris D; Georgitsi M; Drineas P; Paschou P
    BMC Bioinformatics; 2017 Jul; 18(1):341. PubMed ID: 28716001
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Simple ClinVar: an interactive web server to explore and retrieve gene and disease variants aggregated in ClinVar database.
    Pérez-Palma E; Gramm M; Nürnberg P; May P; Lal D
    Nucleic Acids Res; 2019 Jul; 47(W1):W99-W105. PubMed ID: 31114901
    [TBL] [Abstract][Full Text] [Related]  

  • 11. ClinVar Miner: Demonstrating utility of a Web-based tool for viewing and filtering ClinVar data.
    Henrie A; Hemphill SE; Ruiz-Schultz N; Cushman B; DiStefano MT; Azzariti D; Harrison SM; Rehm HL; Eilbeck K
    Hum Mutat; 2018 Aug; 39(8):1051-1060. PubMed ID: 29790234
    [TBL] [Abstract][Full Text] [Related]  

  • 12. OrthoVenn2: a web server for whole-genome comparison and annotation of orthologous clusters across multiple species.
    Xu L; Dong Z; Fang L; Luo Y; Wei Z; Guo H; Zhang G; Gu YQ; Coleman-Derr D; Xia Q; Wang Y
    Nucleic Acids Res; 2019 Jul; 47(W1):W52-W58. PubMed ID: 31053848
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Web-TCGA: an online platform for integrated analysis of molecular cancer data sets.
    Deng M; Brägelmann J; Schultze JL; Perner S
    BMC Bioinformatics; 2016 Feb; 17():72. PubMed ID: 26852330
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DivBrowse-interactive visualization and exploratory data analysis of variant call matrices.
    König P; Beier S; Mascher M; Stein N; Lange M; Scholz U
    Gigascience; 2022 Dec; 12():. PubMed ID: 37083938
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Cancer Genome Atlas Clinical Explorer: a web and mobile interface for identifying clinical-genomic driver associations.
    Lee H; Palm J; Grimes SM; Ji HP
    Genome Med; 2015 Oct; 7():112. PubMed ID: 26507825
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Bystro: rapid online variant annotation and natural-language filtering at whole-genome scale.
    Kotlar AV; Trevino CE; Zwick ME; Cutler DJ; Wingo TS
    Genome Biol; 2018 Feb; 19(1):14. PubMed ID: 29409527
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Scripps Genome ADVISER: Annotation and Distributed Variant Interpretation SERver.
    Pham PH; Shipman WJ; Erikson GA; Schork NJ; Torkamani A
    PLoS One; 2015; 10(2):e0116815. PubMed ID: 25706643
    [TBL] [Abstract][Full Text] [Related]  

  • 18. SNiPA: an interactive, genetic variant-centered annotation browser.
    Arnold M; Raffler J; Pfeufer A; Suhre K; Kastenmüller G
    Bioinformatics; 2015 Apr; 31(8):1334-6. PubMed ID: 25431330
    [TBL] [Abstract][Full Text] [Related]  

  • 19. CRAMER: a lightweight, highly customizable web-based genome browser supporting multiple visualization instances.
    Anastasiadi M; Bragin E; Biojoux P; Ahamed A; Burgin J; de Castro Cogle K; Llaneza-Lago S; Muvunyi R; Scislak M; Aktan I; Molitor C; Kurowski T; Mohareb F
    Bioinformatics; 2020 Jun; 36(11):3556-3557. PubMed ID: 32108858
    [TBL] [Abstract][Full Text] [Related]  

  • 20. VarFish: comprehensive DNA variant analysis for diagnostics and research.
    Holtgrewe M; Stolpe O; Nieminen M; Mundlos S; Knaus A; Kornak U; Seelow D; Segebrecht L; Spielmann M; Fischer-Zirnsak B; Boschann F; Scholl U; Ehmke N; Beule D
    Nucleic Acids Res; 2020 Jul; 48(W1):W162-W169. PubMed ID: 32338743
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.