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 *

105 related articles for article (PubMed ID: 15574202)

  • 1. Haplotype frequency estimation error analysis in the presence of missing genotype data.
    Kelly ED; Sievers F; McManus R
    BMC Bioinformatics; 2004 Dec; 5():188. PubMed ID: 15574202
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Accuracy of haplotype frequency estimation for biallelic loci, via the expectation-maximization algorithm for unphased diploid genotype data.
    Fallin D; Schork NJ
    Am J Hum Genet; 2000 Oct; 67(4):947-59. PubMed ID: 10954684
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Statistical estimation and pedigree analysis of CCR2-CCR5 haplotypes.
    Clark VJ; Metheny N; Dean M; Peterson RJ
    Hum Genet; 2001 Jun; 108(6):484-93. PubMed ID: 11499673
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Characterisation of SNP haplotype structure in chemokine and chemokine receptor genes using CEPH pedigrees and statistical estimation.
    Clark VJ; Dean M
    Hum Genomics; 2004 Mar; 1(3):195-207. PubMed ID: 15588479
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Maximum-likelihood estimation of haplotype frequencies in nuclear families.
    Becker T; Knapp M
    Genet Epidemiol; 2004 Jul; 27(1):21-32. PubMed ID: 15185400
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Quantifying the amount of missing information in genetic association studies.
    Nicolae DL
    Genet Epidemiol; 2006 Dec; 30(8):703-17. PubMed ID: 16986163
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Handling missing values in population data: consequences for maximum likelihood estimation of haplotype frequencies.
    Gourraud PA; Génin E; Cambon-Thomsen A
    Eur J Hum Genet; 2004 Oct; 12(10):805-12. PubMed ID: 15252420
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Analysis of intragenic polymorphic markers of the CFTR gene in cystic fibrosis patients and health donors from Bashkorostan].
    Korytina GF; Viktorova TV; Uvashchenko TE; Baranov VS; Khusnutdinova EK
    Genetika; 2003 Nov; 39(11):1542-9. PubMed ID: 14714468
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Estimating haplotype frequencies and standard errors for multiple single nucleotide polymorphisms.
    Li SS; Khalid N; Carlson C; Zhao LP
    Biostatistics; 2003 Oct; 4(4):513-22. PubMed ID: 14557108
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The impact of missing and erroneous genotypes on tagging SNP selection and power of subsequent association tests.
    Liu W; Zhao W; Chase GA
    Hum Hered; 2006; 61(1):31-44. PubMed ID: 16557026
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Haplotyping and estimation of haplotype frequencies for closely linked biallelic multilocus genetic phenotypes including nuclear family information.
    Rohde K; Fuerst R
    Hum Mutat; 2001 Apr; 17(4):289-95. PubMed ID: 11295827
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Haplotype frequency estimation in patient populations: the effect of departures from Hardy-Weinberg proportions and collapsing over a locus in the HLA region.
    Single RM; Meyer D; Hollenbach JA; Nelson MP; Noble JA; Erlich HA; Thomson G
    Genet Epidemiol; 2002 Feb; 22(2):186-95. PubMed ID: 11788963
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Estimating haplotype frequencies in pooled DNA samples when there is genotyping error.
    Quade SR; Elston RC; Goddard KA
    BMC Genet; 2005 May; 6():25. PubMed ID: 15943883
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Accounting for linkage disequilibrium among markers in linkage analysis: impact of haplotype frequency estimation and molecular haplotypes for a gene in a candidate region for Alzheimer's disease.
    Sieh W; Yu CE; Bird TD; Schellenberg GD; Wijsman EM
    Hum Hered; 2007; 63(1):26-34. PubMed ID: 17215579
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Accounting for haplotype phase uncertainty in linkage disequilibrium estimation.
    Kulle B; Frigessi A; Edvardsen H; Kristensen V; Wojnowski L
    Genet Epidemiol; 2008 Feb; 32(2):168-78. PubMed ID: 17968987
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Comparison of the accuracy of methods of computational haplotype inference using a large empirical dataset.
    Adkins RM
    BMC Genet; 2004 Aug; 5():22. PubMed ID: 15291970
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Haplotype analysis in the presence of informatively missing genotype data.
    Liu N; Beerman I; Lifton R; Zhao H
    Genet Epidemiol; 2006 May; 30(4):290-300. PubMed ID: 16528706
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Haplotype information and linkage disequilibrium mapping for single nucleotide polymorphisms.
    Lu X; Niu T; Liu JS
    Genome Res; 2003 Sep; 13(9):2112-7. PubMed ID: 12952879
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Notes on the maximum likelihood estimation of haplotype frequencies.
    Mano S; Yasuda N; Katoh T; Tounai K; Inoko H; Imanishi T; Tamiya G; Gojobori T
    Ann Hum Genet; 2004 May; 68(Pt 3):257-64. PubMed ID: 15180706
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.