BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

65 related articles for article (PubMed ID: 25742008)

  • 1. Should we have blind faith in bioinformatics software? Illustrations from the SNAP web-based tool.
    Robiou-du-Pont S; Li A; Christie S; Sohani ZN; Meyre D
    PLoS One; 2015; 10(3):e0118925. PubMed ID: 25742008
    [TBL] [Abstract][Full Text] [Related]  

  • 2. SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap.
    Johnson AD; Handsaker RE; Pulit SL; Nizzari MM; O'Donnell CJ; de Bakker PI
    Bioinformatics; 2008 Dec; 24(24):2938-9. PubMed ID: 18974171
    [TBL] [Abstract][Full Text] [Related]  

  • 3. SNPdetector: a software tool for sensitive and accurate SNP detection.
    Zhang J; Wheeler DA; Yakub I; Wei S; Sood R; Rowe W; Liu PP; Gibbs RA; Buetow KH
    PLoS Comput Biol; 2005 Oct; 1(5):e53. PubMed ID: 16261194
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Effect of genome-wide genotyping and reference panels on rare variants imputation.
    Zheng HF; Ladouceur M; Greenwood CM; Richards JB
    J Genet Genomics; 2012 Oct; 39(10):545-50. PubMed ID: 23089364
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A web-based tool to retrieve human genome polymorphisms from public databases.
    Riva A; Kohane IS
    Proc AMIA Symp; 2001; ():558-62. PubMed ID: 11825250
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays.
    Di X; Matsuzaki H; Webster TA; Hubbell E; Liu G; Dong S; Bartell D; Huang J; Chiles R; Yang G; Shen MM; Kulp D; Kennedy GC; Mei R; Jones KW; Cawley S
    Bioinformatics; 2005 May; 21(9):1958-63. PubMed ID: 15657097
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Functional evaluation of genetic variants associated with endometriosis near GREB1.
    Fung JN; Holdsworth-Carson SJ; Sapkota Y; Zhao ZZ; Jones L; Girling JE; Paiva P; Healey M; Nyholt DR; Rogers PA; Montgomery GW
    Hum Reprod; 2015 May; 30(5):1263-75. PubMed ID: 25788566
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A tool for selecting SNPs for association studies based on observed linkage disequilibrium patterns.
    De La Vega FM; Isaac HI; Scafe CR
    Pac Symp Biocomput; 2006; ():487-98. PubMed ID: 17094263
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Selecting single-nucleotide polymorphisms for association studies with SNPbrowser software.
    De La Vega FM
    Methods Mol Biol; 2007; 376():177-93. PubMed ID: 17984546
    [TBL] [Abstract][Full Text] [Related]  

  • 10. SNPselector: a web tool for selecting SNPs for genetic association studies.
    Xu H; Gregory SG; Hauser ER; Stenger JE; Pericak-Vance MA; Vance JM; Züchner S; Hauser MA
    Bioinformatics; 2005 Nov; 21(22):4181-6. PubMed ID: 16179360
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Power analysis for genome-wide association studies.
    Klein RJ
    BMC Genet; 2007 Aug; 8():58. PubMed ID: 17725844
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Current bioinformatics tools in genomic biomedical research (Review).
    Teufel A; Krupp M; Weinmann A; Galle PR
    Int J Mol Med; 2006 Jun; 17(6):967-73. PubMed ID: 16685403
    [TBL] [Abstract][Full Text] [Related]  

  • 13. QuickSNP: an automated web server for selection of tagSNPs.
    Grover D; Woodfield AS; Verma R; Zandi PP; Levinson DF; Potash JB
    Nucleic Acids Res; 2007 Jul; 35(Web Server issue):W115-20. PubMed ID: 17517769
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Family-Based Benchmarking of Copy Number Variation Detection Software.
    Nutsua ME; Fischer A; Nebel A; Hofmann S; Schreiber S; Krawczak M; Nothnagel M
    PLoS One; 2015; 10(7):e0133465. PubMed ID: 26197066
    [TBL] [Abstract][Full Text] [Related]  

  • 15. V-MitoSNP: visualization of human mitochondrial SNPs.
    Chuang LY; Yang CH; Cheng YH; Gu DL; Chang PL; Tsui KH; Chang HW
    BMC Bioinformatics; 2006 Aug; 7():379. PubMed ID: 16907992
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Navigating the HapMap.
    Barnes MR
    Brief Bioinform; 2006 Sep; 7(3):211-24. PubMed ID: 16877472
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Frequently used bioinformatics tools overestimate the damaging effect of allelic variants.
    Andersen LL; Terczyńska-Dyla E; Mørk N; Scavenius C; Enghild JJ; Höning K; Hornung V; Christiansen M; Mogensen TH; Hartmann R
    Genes Immun; 2019 Jan; 20(1):10-22. PubMed ID: 29217828
    [TBL] [Abstract][Full Text] [Related]  

  • 18. HapMap filter 1.0: a tool to preprocess the HapMap genotypic data for association studies.
    Zhang W; Duan S; Dolan ME
    Bioinformation; 2008 May; 2(8):322-4. PubMed ID: 18685717
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Retrieving HapMap Data Using HapMart.
    Smith AV
    CSH Protoc; 2008 Jul; 2008():pdb.prot5026. PubMed ID: 21356870
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Use of Transgenes and Mutations in the Mouse to Study the Genetic Basis of Locomotor Hyperactivity.
    Hess EJ
    Methods; 1996 Dec; 10(3):374-83. PubMed ID: 8954849
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.