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 *

66 related articles for article (PubMed ID: 21356868)

  • 21. Tag SNP selection for candidate gene association studies using HapMap and gene resequencing data.
    Xu Z; Kaplan NL; Taylor JA
    Eur J Hum Genet; 2007 Oct; 15(10):1063-70. PubMed ID: 17568388
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Whole-genome genotyping of haplotype tag single nucleotide polymorphisms.
    Gunderson KL; Kuhn KM; Steemers FJ; Ng P; Murray SS; Shen R
    Pharmacogenomics; 2006 Jun; 7(4):641-8. PubMed ID: 16768648
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. The effect of single-nucleotide polymorphism marker selection on patterns of haplotype blocks and haplotype frequency estimates.
    Nothnagel M; Rohde K
    Am J Hum Genet; 2005 Dec; 77(6):988-98. PubMed ID: 16380910
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Comparison of variation in frequency for SNPs associated with asthma or liver disease between Estonia, HapMap populations and the 1000 genome project populations.
    Reisberg S; Galwey N; Avillach P; Sahlqvist AS; Kolberg L; Mägi R; Esko T; Vilo J; James G
    Int J Immunogenet; 2019 Apr; 46(2):49-58. PubMed ID: 30659741
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Perspectives on human genetic variation from the HapMap Project.
    McVean G; Spencer CC; Chaix R
    PLoS Genet; 2005 Oct; 1(4):e54. PubMed ID: 16254603
    [TBL] [Abstract][Full Text] [Related]  

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

  • 28. Evaluating coverage of exons by HapMap SNPs.
    Dong X; Zhong T; Xu T; Xia Y; Li B; Li C; Yuan L; Ding G; Li Y
    Genomics; 2013 Jan; 101(1):20-3. PubMed ID: 23000193
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

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

  • 31. Prediction of disease-associated single nucleotide polymorphisms using virtual genomes constructed from a public haplotype database.
    Toyabe S; Miyashita A; Kitamura N; Kuwano R; Akazawa K
    Methods Inf Med; 2008; 47(6):522-8. PubMed ID: 19057809
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. The ENCODE Project at UC Santa Cruz.
    Thomas DJ; Rosenbloom KR; Clawson H; Hinrichs AS; Trumbower H; Raney BJ; Karolchik D; Barber GP; Harte RA; Hillman-Jackson J; Kuhn RM; Rhead BL; Smith KE; Thakkapallayil A; Zweig AS; ; Haussler D; Kent WJ
    Nucleic Acids Res; 2007 Jan; 35(Database issue):D663-7. PubMed ID: 17166863
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Tag SNP selection for association studies.
    Stram DO
    Genet Epidemiol; 2004 Dec; 27(4):365-74. PubMed ID: 15372618
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Genetic variation and human longevity.
    Soerensen M
    Dan Med J; 2012 May; 59(5):B4454. PubMed ID: 22549493
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Transferability of tag SNPs in genetic association studies in multiple populations.
    de Bakker PI; Burtt NP; Graham RR; Guiducci C; Yelensky R; Drake JA; Bersaglieri T; Penney KL; Butler J; Young S; Onofrio RC; Lyon HN; Stram DO; Haiman CA; Freedman ML; Zhu X; Cooper R; Groop L; Kolonel LN; Henderson BE; Daly MJ; Hirschhorn JN; Altshuler D
    Nat Genet; 2006 Nov; 38(11):1298-303. PubMed ID: 17057720
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Analysis of high-resolution HapMap of DTNBP1 (Dysbindin) suggests no consistency between reported common variant associations and schizophrenia.
    Mutsuddi M; Morris DW; Waggoner SG; Daly MJ; Scolnick EM; Sklar P
    Am J Hum Genet; 2006 Nov; 79(5):903-9. PubMed ID: 17033966
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Using haplotype blocks to map human complex trait loci.
    Cardon LR; Abecasis GR
    Trends Genet; 2003 Mar; 19(3):135-40. PubMed ID: 12615007
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.