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 *

130 related articles for article (PubMed ID: 19208179)

  • 1. A fast algorithm for genome-wide haplotype pattern mining.
    Besenbacher S; Pedersen CN; Mailund T
    BMC Bioinformatics; 2009 Jan; 10 Suppl 1(Suppl 1):S74. PubMed ID: 19208179
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detecting genome wide haplotype sharing using SNP or microsatellite haplotype data.
    Bahlo M; Stankovich J; Speed TP; Rubio JP; Burfoot RK; Foote SJ
    Hum Genet; 2006 Mar; 119(1-2):38-50. PubMed ID: 16362347
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering.
    Browning SR; Browning BL
    Am J Hum Genet; 2007 Nov; 81(5):1084-97. PubMed ID: 17924348
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Haplotype-based linkage disequilibrium mapping via direct data mining.
    Li J; Jiang T
    Bioinformatics; 2005 Dec; 21(24):4384-93. PubMed ID: 16249262
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Data mining applied to linkage disequilibrium mapping.
    Toivonen HT; Onkamo P; Vasko K; Ollikainen V; Sevon P; Mannila H; Herr M; Kere J
    Am J Hum Genet; 2000 Jul; 67(1):133-45. PubMed ID: 10848493
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. GenHap: a novel computational method based on genetic algorithms for haplotype assembly.
    Tangherloni A; Spolaor S; Rundo L; Nobile MS; Cazzaniga P; Mauri G; LiĆ² P; Merelli I; Besozzi D
    BMC Bioinformatics; 2019 Apr; 20(Suppl 4):172. PubMed ID: 30999845
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Selecting additional tag SNPs for tolerating missing data in genotyping.
    Huang YT; Zhang K; Chen T; Chao KM
    BMC Bioinformatics; 2005 Nov; 6():263. PubMed ID: 16259642
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A double classification tree search algorithm for index SNP selection.
    Zhang P; Sheng H; Uehara R
    BMC Bioinformatics; 2004 Jul; 5():89. PubMed ID: 15238162
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Haplotype block partitioning and tag SNP selection using genotype data and their applications to association studies.
    Zhang K; Qin ZS; Liu JS; Chen T; Waterman MS; Sun F
    Genome Res; 2004 May; 14(5):908-16. PubMed ID: 15078859
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Optimal step length EM algorithm (OSLEM) for the estimation of haplotype frequency and its application in lipoprotein lipase genotyping.
    Zhang P; Sheng H; Morabia A; Gilliam TC
    BMC Bioinformatics; 2003 Jan; 4():3. PubMed ID: 12529185
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel haplotype-sharing approach for genome-wide case-control association studies implicates the calpastatin gene in Parkinson's disease.
    Allen AS; Satten GA
    Genet Epidemiol; 2009 Dec; 33(8):657-67. PubMed ID: 19365859
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Utilizing HapMap and tagging SNPs.
    Haiman CA; Stram DO
    Methods Mol Med; 2008; 141():37-54. PubMed ID: 18453083
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cloud computing-based TagSNP selection algorithm for human genome data.
    Hung CL; Chen WP; Hua GJ; Zheng H; Tsai SJ; Lin YL
    Int J Mol Sci; 2015 Jan; 16(1):1096-110. PubMed ID: 25569088
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exhaustive allelic transmission disequilibrium tests as a new approach to genome-wide association studies.
    Lin S; Chakravarti A; Cutler DJ
    Nat Genet; 2004 Nov; 36(11):1181-8. PubMed ID: 15502828
    [TBL] [Abstract][Full Text] [Related]  

  • 18. SNP haplotype tagging from DNA pools of two individuals.
    Hoh J; Matsuda F; Peng X; Markovic D; Lathrop MG; Ott J
    BMC Bioinformatics; 2003 Apr; 4():14. PubMed ID: 12709267
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Computational intelligence in bioinformatics: SNP/haplotype data in genetic association study for common diseases.
    Kelemen A; Vasilakos AV; Liang Y
    IEEE Trans Inf Technol Biomed; 2009 Sep; 13(5):841-7. PubMed ID: 19556205
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The relative power of SNPs and haplotype as genetic markers for association tests.
    Bader JS
    Pharmacogenomics; 2001 Feb; 2(1):11-24. PubMed ID: 11258193
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.