BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

85 related articles for article (PubMed ID: 12446872)

  • 1. Are 100,000 "SNPs" useless?
    Hurles M
    Science; 2002 Nov; 298(5598):1509; author reply 1509. PubMed ID: 12446872
    [No Abstract]   [Full Text] [Related]  

  • 2. Introduction to SNPs: discovery of markers for disease.
    Weiner MP; Hudson TJ
    Biotechniques; 2002 Jun; Suppl():4-7, 10, 12-3. PubMed ID: 12083396
    [No Abstract]   [Full Text] [Related]  

  • 3. Quality and completeness of SNP databases.
    Reich DE; Gabriel SB; Altshuler D
    Nat Genet; 2003 Apr; 33(4):457-8. PubMed ID: 12652301
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Structural variants deconstruct the genome.
    Nat Genet; 2006 Sep; 38(9):959. PubMed ID: 16940994
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The challenge of using SNPs in the understanding and treatment of disease.
    Schifreen RS; Storts DR; Buller AM
    Biotechniques; 2002 Jun; Suppl():14-6, 18, 20-1. PubMed ID: 12083392
    [No Abstract]   [Full Text] [Related]  

  • 6. Genomics. 1000 Genomes Project gives new map of genetic diversity.
    Pennisi E
    Science; 2010 Oct; 330(6004):574-5. PubMed ID: 21030618
    [No Abstract]   [Full Text] [Related]  

  • 7. Genome structural variation and sporadic disease traits.
    Lupski JR
    Nat Genet; 2006 Sep; 38(9):974-6. PubMed ID: 16941003
    [No Abstract]   [Full Text] [Related]  

  • 8. Life, diversity and the pursuit of haplotypes.
    McCarthy J
    Nat Biotechnol; 2005 Nov; 23(11):1376-7. PubMed ID: 16273067
    [No Abstract]   [Full Text] [Related]  

  • 9. FESD: a Functional Element SNPs Database in human.
    Kang HJ; Choi KO; Kim BD; Kim S; Kim YJ
    Nucleic Acids Res; 2005 Jan; 33(Database issue):D518-22. PubMed ID: 15608252
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Singleton SNPs in the human genome and implications for genome-wide association studies.
    Ke X; Taylor MS; Cardon LR
    Eur J Hum Genet; 2008 Apr; 16(4):506-15. PubMed ID: 18197193
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evaluation of coverage variation of SNP chips for genome-wide association studies.
    Li M; Li C; Guan W
    Eur J Hum Genet; 2008 May; 16(5):635-43. PubMed ID: 18253166
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Single nucleotide polymorphism in transcriptional regulatory regions and expression of environmentally responsive genes.
    Wang X; Tomso DJ; Liu X; Bell DA
    Toxicol Appl Pharmacol; 2005 Sep; 207(2 Suppl):84-90. PubMed ID: 16002116
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complex SNP-related sequence variation in segmental genome duplications.
    Fredman D; White SJ; Potter S; Eichler EE; Den Dunnen JT; Brookes AJ
    Nat Genet; 2004 Aug; 36(8):861-6. PubMed ID: 15247918
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comparison of fine-scale recombination rates in humans and chimpanzees.
    Winckler W; Myers SR; Richter DJ; Onofrio RC; McDonald GJ; Bontrop RE; McVean GA; Gabriel SB; Reich D; Donnelly P; Altshuler D
    Science; 2005 Apr; 308(5718):107-11. PubMed ID: 15705809
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Analysis and application of SNP and haplotype in the human genome].
    Li J; Pan YC; Li YX; Shi TL
    Yi Chuan Xue Bao; 2005 Aug; 32(8):879-89. PubMed ID: 16231744
    [TBL] [Abstract][Full Text] [Related]  

  • 16. SNP-VISTA: an interactive SNP visualization tool.
    Shah N; Teplitsky MV; Minovitsky S; Pennacchio LA; Hugenholtz P; Hamann B; Dubchak IL
    BMC Bioinformatics; 2005 Dec; 6():292. PubMed ID: 16336665
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Polymorphic segmental duplications at 8p23.1 challenge the determination of individual defensin gene repertoires and the assembly of a contiguous human reference sequence.
    Taudien S; Galgoczy P; Huse K; Reichwald K; Schilhabel M; Szafranski K; Shimizu A; Asakawa S; Frankish A; Loncarevic IF; Shimizu N; Siddiqui R; Platzer M
    BMC Genomics; 2004 Dec; 5(1):92. PubMed ID: 15588320
    [TBL] [Abstract][Full Text] [Related]  

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

  • 19. Targeted screening of cis-regulatory variation in human haplotypes.
    Verlaan DJ; Ge B; Grundberg E; Hoberman R; Lam KC; Koka V; Dias J; Gurd S; Martin NW; Mallmin H; Nilsson O; Harmsen E; Dewar K; Kwan T; Pastinen T
    Genome Res; 2009 Jan; 19(1):118-27. PubMed ID: 18971308
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pharmacogenetics and genotyping: on the trail of SNPs.
    Melton L
    Nature; 2003 Apr; 422(6934):917, 919, 921, 923. PubMed ID: 12712209
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.