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 *

174 related articles for article (PubMed ID: 18617537)

  • 1. Multimarker analysis and imputation of multiple platform pooling-based genome-wide association studies.
    Homer N; Tembe WD; Szelinger S; Redman M; Stephan DA; Pearson JV; Nelson SF; Craig D
    Bioinformatics; 2008 Sep; 24(17):1896-902. PubMed ID: 18617537
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genome-wide selection of tag SNPs using multiple-marker correlation.
    Hao K
    Bioinformatics; 2007 Dec; 23(23):3178-84. PubMed ID: 18006555
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A survey on haplotyping algorithms for tightly linked markers.
    Li J; Jiang T
    J Bioinform Comput Biol; 2008 Feb; 6(1):241-59. PubMed ID: 18324755
    [TBL] [Abstract][Full Text] [Related]  

  • 4. FastTagger: an efficient algorithm for genome-wide tag SNP selection using multi-marker linkage disequilibrium.
    Liu G; Wang Y; Wong L
    BMC Bioinformatics; 2010 Jan; 11():66. PubMed ID: 20113476
    [TBL] [Abstract][Full Text] [Related]  

  • 5. LdCompare: rapid computation of single- and multiple-marker r2 and genetic coverage.
    Hao K; Di X; Cawley S
    Bioinformatics; 2007 Jan; 23(2):252-4. PubMed ID: 17148510
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies.
    Hao K; Chudin E; McElwee J; Schadt EE
    BMC Genet; 2009 Jun; 10():27. PubMed ID: 19531258
    [TBL] [Abstract][Full Text] [Related]  

  • 7. ssSNPer: identifying statistically similar SNPs to aid interpretation of genetic association studies.
    Nyholt DR
    Bioinformatics; 2006 Dec; 22(23):2960-1. PubMed ID: 17038340
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Comparison of multimarker logistic regression models, with application to a genomewide scan of schizophrenia.
    Wason JM; Dudbridge F
    BMC Genet; 2010 Sep; 11():80. PubMed ID: 20828390
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Efficiency and power in genetic association studies.
    de Bakker PI; Yelensky R; Pe'er I; Gabriel SB; Daly MJ; Altshuler D
    Nat Genet; 2005 Nov; 37(11):1217-23. PubMed ID: 16244653
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Snagger: a user-friendly program for incorporating additional information for tagSNP selection.
    Edlund CK; Lee WH; Li D; Van Den Berg DJ; Conti DV
    BMC Bioinformatics; 2008 Mar; 9():174. PubMed ID: 18371222
    [TBL] [Abstract][Full Text] [Related]  

  • 11. TAGster: efficient selection of LD tag SNPs in single or multiple populations.
    Xu Z; Kaplan NL; Taylor JA
    Bioinformatics; 2007 Dec; 23(23):3254-5. PubMed ID: 17827206
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fine mapping by composite genome-wide association analysis.
    Casellas J; Cañas-Álvarez JJ; Fina M; Piedrafita J; Cecchinato A
    Genet Res (Camb); 2017 Jun; 99():e4. PubMed ID: 28583209
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Haplotype block structure and its applications to association studies: power and study designs.
    Zhang K; Calabrese P; Nordborg M; Sun F
    Am J Hum Genet; 2002 Dec; 71(6):1386-94. PubMed ID: 12439824
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Effects of single SNPs, haplotypes, and whole-genome LD maps on accuracy of association mapping.
    Maniatis N; Collins A; Morton NE
    Genet Epidemiol; 2007 Apr; 31(3):179-88. PubMed ID: 17285621
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Choosing SNPs using feature selection.
    Phuong TM; Lin Z; Altman RB
    Proc IEEE Comput Syst Bioinform Conf; 2005; ():301-9. PubMed ID: 16447987
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set.
    Nicolae DL; Wen X; Voight BF; Cox NJ
    PLoS Genet; 2006 May; 2(5):e67. PubMed ID: 16680197
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Leveraging the HapMap correlation structure in association studies.
    Zaitlen N; Kang HM; Eskin E; Halperin E
    Am J Hum Genet; 2007 Apr; 80(4):683-91. PubMed ID: 17357074
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Inference of missing SNPs and information quantity measurements for haplotype blocks.
    Su SC; Kuo CC; Chen T
    Bioinformatics; 2005 May; 21(9):2001-7. PubMed ID: 15699029
    [TBL] [Abstract][Full Text] [Related]  

  • 19. HapBlock: haplotype block partitioning and tag SNP selection software using a set of dynamic programming algorithms.
    Zhang K; Qin Z; Chen T; Liu JS; Waterman MS; Sun F
    Bioinformatics; 2005 Jan; 21(1):131-4. PubMed ID: 15333454
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of LD structures and the utility of HapMap in genetic association studies.
    Gu CC; Yu K; Rao DC
    Adv Genet; 2008; 60():407-35. PubMed ID: 18358328
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.