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 *

129 related articles for article (PubMed ID: 19297347)

  • 21. The MiSink Plugin: Cytoscape as a graphical interface to the Database of Interacting Proteins.
    Salwinski L; Eisenberg D
    Bioinformatics; 2007 Aug; 23(16):2193-5. PubMed ID: 17553858
    [TBL] [Abstract][Full Text] [Related]  

  • 22. VistaClara: an expression browser plug-in for Cytoscape.
    Kincaid R; Kuchinsky A; Creech M
    Bioinformatics; 2008 Sep; 24(18):2112-4. PubMed ID: 18678589
    [TBL] [Abstract][Full Text] [Related]  

  • 23. PROMOT: modular modeling for systems biology.
    Mirschel S; Steinmetz K; Rempel M; Ginkel M; Gilles ED
    Bioinformatics; 2009 Mar; 25(5):687-9. PubMed ID: 19147665
    [TBL] [Abstract][Full Text] [Related]  

  • 24. PupaSuite: finding functional single nucleotide polymorphisms for large-scale genotyping purposes.
    Conde L; Vaquerizas JM; Dopazo H; Arbiza L; Reumers J; Rousseau F; Schymkowitz J; Dopazo J
    Nucleic Acids Res; 2006 Jul; 34(Web Server issue):W621-5. PubMed ID: 16845085
    [TBL] [Abstract][Full Text] [Related]  

  • 25. SNPNB: analyzing neighboring-nucleotide biases on single nucleotide polymorphisms (SNPs).
    Zhang F; Zhao Z
    Bioinformatics; 2005 May; 21(10):2517-9. PubMed ID: 15769840
    [TBL] [Abstract][Full Text] [Related]  

  • 26. CAVER Analyst 1.0: graphic tool for interactive visualization and analysis of tunnels and channels in protein structures.
    Kozlikova B; Sebestova E; Sustr V; Brezovsky J; Strnad O; Daniel L; Bednar D; Pavelka A; Manak M; Bezdeka M; Benes P; Kotry M; Gora A; Damborsky J; Sochor J
    Bioinformatics; 2014 Sep; 30(18):2684-5. PubMed ID: 24876375
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Complex Trait Analyses of the Collaborative Cross: Tools and Databases.
    Ram R; Morahan G
    Methods Mol Biol; 2017; 1488():121-129. PubMed ID: 27933522
    [TBL] [Abstract][Full Text] [Related]  

  • 28. GeneSpy, a user-friendly and flexible genomic context visualizer.
    Garcia PS; Jauffrit F; Grangeasse C; Brochier-Armanet C
    Bioinformatics; 2019 Jan; 35(2):329-331. PubMed ID: 29912383
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Providing context and interpretability to genetic association analysis results using the KGraph.
    Kelly RJ; Smith JA; Kardia SL
    Adv Genet; 2010; 72():181-93. PubMed ID: 21029853
    [TBL] [Abstract][Full Text] [Related]  

  • 30. HapScope: a software system for automated and visual analysis of functionally annotated haplotypes.
    Zhang J; Rowe WL; Struewing JP; Buetow KH
    Nucleic Acids Res; 2002 Dec; 30(23):5213-21. PubMed ID: 12466546
    [TBL] [Abstract][Full Text] [Related]  

  • 31. varLD: a program for quantifying variation in linkage disequilibrium patterns between populations.
    Ong RT; Teo YY
    Bioinformatics; 2010 May; 26(9):1269-70. PubMed ID: 20308177
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Chi8: a GPU program for detecting significant interacting SNPs with the Chi-square 8-df test.
    Al-jouie A; Esfandiari M; Ramakrishnan S; Roshan U
    BMC Res Notes; 2015 Sep; 8():436. PubMed ID: 26369336
    [TBL] [Abstract][Full Text] [Related]  

  • 33. minimac2: faster genotype imputation.
    Fuchsberger C; Abecasis GR; Hinds DA
    Bioinformatics; 2015 Mar; 31(5):782-4. PubMed ID: 25338720
    [TBL] [Abstract][Full Text] [Related]  

  • 34. SNP2RFLP: a computational tool to facilitate genetic mapping using benchtop analysis of SNPs.
    Beckstead WA; Bjork BC; Stottmann RW; Sunyaev S; Beier DR
    Mamm Genome; 2008; 19(10-12):687-90. PubMed ID: 18958524
    [TBL] [Abstract][Full Text] [Related]  

  • 35. LocusZoom: regional visualization of genome-wide association scan results.
    Pruim RJ; Welch RP; Sanna S; Teslovich TM; Chines PS; Gliedt TP; Boehnke M; Abecasis GR; Willer CJ
    Bioinformatics; 2010 Sep; 26(18):2336-7. PubMed ID: 20634204
    [TBL] [Abstract][Full Text] [Related]  

  • 36. HapBoost: a fast approach to boosting haplotype association analyses in genome-wide association studies.
    Wan X; Yang C; Yang Q; Zhao H; Yu W
    IEEE/ACM Trans Comput Biol Bioinform; 2013; 10(1):207-12. PubMed ID: 23702557
    [TBL] [Abstract][Full Text] [Related]  

  • 37. htSNPer1.0: software for haplotype block partition and htSNPs selection.
    Ding K; Zhang J; Zhou K; Shen Y; Zhang X
    BMC Bioinformatics; 2005 Mar; 6():38. PubMed ID: 15740612
    [TBL] [Abstract][Full Text] [Related]  

  • 38. GeneCruiser: a web service for the annotation of microarray data.
    Liefeld T; Reich M; Gould J; Zhang P; Tamayo P; Mesirov JP
    Bioinformatics; 2005 Sep; 21(18):3681-2. PubMed ID: 16030072
    [TBL] [Abstract][Full Text] [Related]  

  • 39. PupasView: a visual tool for selecting suitable SNPs, with putative pathological effect in genes, for genotyping purposes.
    Conde L; Vaquerizas JM; Ferrer-Costa C; de la Cruz X; Orozco M; Dopazo J
    Nucleic Acids Res; 2005 Jul; 33(Web Server issue):W501-5. PubMed ID: 15980522
    [TBL] [Abstract][Full Text] [Related]  

  • 40. PGA: power calculator for case-control genetic association analyses.
    Menashe I; Rosenberg PS; Chen BE
    BMC Genet; 2008 May; 9():36. PubMed ID: 18477402
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.