BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 14751981)

  • 1. Large-scale analysis of non-synonymous coding region single nucleotide polymorphisms.
    Clifford RJ; Edmonson MN; Nguyen C; Buetow KH
    Bioinformatics; 2004 May; 20(7):1006-14. PubMed ID: 14751981
    [TBL] [Abstract][Full Text] [Related]  

  • 2. LS-SNP: large-scale annotation of coding non-synonymous SNPs based on multiple information sources.
    Karchin R; Diekhans M; Kelly L; Thomas DJ; Pieper U; Eswar N; Haussler D; Sali A
    Bioinformatics; 2005 Jun; 21(12):2814-20. PubMed ID: 15827081
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Prediction of the phenotypic effects of non-synonymous single nucleotide polymorphisms using structural and evolutionary information.
    Bao L; Cui Y
    Bioinformatics; 2005 May; 21(10):2185-90. PubMed ID: 15746281
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Structure SNP (StSNP): a web server for mapping and modeling nsSNPs on protein structures with linkage to metabolic pathways.
    Uzun A; Leslin CM; Abyzov A; Ilyin V
    Nucleic Acids Res; 2007 Jul; 35(Web Server issue):W384-92. PubMed ID: 17537826
    [TBL] [Abstract][Full Text] [Related]  

  • 5. SNP@Domain: a web resource of single nucleotide polymorphisms (SNPs) within protein domain structures and sequences.
    Han A; Kang HJ; Cho Y; Lee S; Kim YJ; Gong S
    Nucleic Acids Res; 2006 Jul; 34(Web Server issue):W642-4. PubMed ID: 16845090
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Efficient discovery of single-nucleotide polymorphisms in coding regions of human genes.
    Hu G; Modrek B; Riise Stensland HM; Saarela J; Pajukanta P; Kustanovich V; Peltonen L; Nelson SF; Lee C
    Pharmacogenomics J; 2002; 2(4):236-42. PubMed ID: 12196912
    [TBL] [Abstract][Full Text] [Related]  

  • 7. SNP mining porcine ESTs with MAVIANT, a novel tool for SNP evaluation and annotation.
    Panitz F; Stengaard H; Hornshøj H; Gorodkin J; Hedegaard J; Cirera S; Thomsen B; Madsen LB; Høj A; Vingborg RK; Zahn B; Wang X; Wang X; Wernersson R; Jørgensen CB; Scheibye-Knudsen K; Arvin T; Lumholdt S; Sawera M; Green T; Nielsen BJ; Havgaard JH; Brunak S; Fredholm M; Bendixen C
    Bioinformatics; 2007 Jul; 23(13):i387-91. PubMed ID: 17646321
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic diversity and function in the human cytosolic sulfotransferases.
    Hildebrandt MA; Carrington DP; Thomae BA; Eckloff BW; Schaid DJ; Yee VC; Weinshilboum RM; Wieben ED
    Pharmacogenomics J; 2007 Apr; 7(2):133-43. PubMed ID: 16801938
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Impact of single nucleotide polymorphisms in HBB gene causing haemoglobinopathies: in silico analysis.
    George Priya Doss C; Rao S
    N Biotechnol; 2009 Apr; 25(4):214-9. PubMed ID: 19429541
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Predicting protein stability changes from sequences using support vector machines.
    Capriotti E; Fariselli P; Calabrese R; Casadio R
    Bioinformatics; 2005 Sep; 21 Suppl 2():ii54-8. PubMed ID: 16204125
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Selective pressures at a codon-level predict deleterious mutations in human disease genes.
    Arbiza L; Duchi S; Montaner D; Burguet J; Pantoja-Uceda D; Pineda-Lucena A; Dopazo J; Dopazo H
    J Mol Biol; 2006 May; 358(5):1390-404. PubMed ID: 16584746
    [TBL] [Abstract][Full Text] [Related]  

  • 12. MINER: software for phylogenetic motif identification.
    La D; Livesay DR
    Nucleic Acids Res; 2005 Jul; 33(Web Server issue):W267-70. PubMed ID: 15980467
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Correlation and prediction of gene expression level from amino acid and dipeptide composition of its protein.
    Raghava GP; Han JH
    BMC Bioinformatics; 2005 Mar; 6():59. PubMed ID: 15773999
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new progressive-iterative algorithm for multiple structure alignment.
    Lupyan D; Leo-Macias A; Ortiz AR
    Bioinformatics; 2005 Aug; 21(15):3255-63. PubMed ID: 15941743
    [TBL] [Abstract][Full Text] [Related]  

  • 15. transAlign: using amino acids to facilitate the multiple alignment of protein-coding DNA sequences.
    Bininda-Emonds OR
    BMC Bioinformatics; 2005 Jun; 6():156. PubMed ID: 15969769
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Characterization of single-nucleotide polymorphisms in coding regions of human genes.
    Cargill M; Altshuler D; Ireland J; Sklar P; Ardlie K; Patil N; Shaw N; Lane CR; Lim EP; Kalyanaraman N; Nemesh J; Ziaugra L; Friedland L; Rolfe A; Warrington J; Lipshutz R; Daley GQ; Lander ES
    Nat Genet; 1999 Jul; 22(3):231-8. PubMed ID: 10391209
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Statistical geometry based prediction of nonsynonymous SNP functional effects using random forest and neuro-fuzzy classifiers.
    Barenboim M; Masso M; Vaisman II; Jamison DC
    Proteins; 2008 Jun; 71(4):1930-9. PubMed ID: 18186470
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Bioinformatics tools for single nucleotide polymorphism discovery and analysis.
    Clifford RJ; Edmonson MN; Nguyen C; Scherpbier T; Hu Y; Buetow KH
    Ann N Y Acad Sci; 2004 May; 1020():101-9. PubMed ID: 15208187
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information.
    Capriotti E; Calabrese R; Casadio R
    Bioinformatics; 2006 Nov; 22(22):2729-34. PubMed ID: 16895930
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Candidate nsSNPs that can affect the functions and interactions of cell cycle proteins.
    Savas S; Ahmad MF; Shariff M; Kim DY; Ozcelik H
    Proteins; 2005 Feb; 58(3):697-705. PubMed ID: 15617026
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.