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 *

196 related articles for article (PubMed ID: 21811076)

  • 1. PSEUDOMARKER: a powerful program for joint linkage and/or linkage disequilibrium analysis on mixtures of singletons and related individuals.
    Hiekkalinna T; Schäffer AA; Lambert B; Norrgrann P; Göring HH; Terwilliger JD
    Hum Hered; 2011; 71(4):256-66. PubMed ID: 21811076
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified.
    Göring HH; Terwilliger JD
    Am J Hum Genet; 2000 Apr; 66(4):1310-27. PubMed ID: 10731466
    [TBL] [Abstract][Full Text] [Related]  

  • 3. PSEUDOMARKER 2.0: efficient computation of likelihoods using NOMAD.
    Gertz EM; Hiekkalinna T; Digabel SL; Audet C; Terwilliger JD; Schäffer AA
    BMC Bioinformatics; 2014 Feb; 15():47. PubMed ID: 24533837
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Improved methods for multi-trait fine mapping of pleiotropic risk loci.
    Kichaev G; Roytman M; Johnson R; Eskin E; Lindström S; Kraft P; Pasaniuc B
    Bioinformatics; 2017 Jan; 33(2):248-255. PubMed ID: 27663501
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Construction of high-quality recombination maps with low-coverage genomic sequencing for joint linkage analysis in maize.
    Li C; Li Y; Bradbury PJ; Wu X; Shi Y; Song Y; Zhang D; Rodgers-Melnick E; Buckler ES; Zhang Z; Li Y; Wang T
    BMC Biol; 2015 Sep; 13():78. PubMed ID: 26390990
    [TBL] [Abstract][Full Text] [Related]  

  • 6. ATRIUM: testing untyped SNPs in case-control association studies with related individuals.
    Wang Z; McPeek MS
    Am J Hum Genet; 2009 Nov; 85(5):667-78. PubMed ID: 19913122
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Combined linkage and linkage disequilibrium mapping for genome screens.
    Xiong M; Jin L
    Genet Epidemiol; 2000 Oct; 19(3):211-34. PubMed ID: 11015125
    [TBL] [Abstract][Full Text] [Related]  

  • 8. mixIndependR: a R package for statistical independence testing of loci in database of multi-locus genotypes.
    Song B; Woerner AE; Planz J
    BMC Bioinformatics; 2021 Jan; 22(1):12. PubMed ID: 33407074
    [TBL] [Abstract][Full Text] [Related]  

  • 9. On the statistical properties of family-based association tests in datasets containing both pedigrees and unrelated case-control samples.
    Hiekkalinna T; Göring HH; Lambert B; Weiss KM; Norrgrann P; Schäffer AA; Terwilliger JD
    Eur J Hum Genet; 2012 Feb; 20(2):217-23. PubMed ID: 21934707
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genome-wide two-marker linkage disequilibrium mapping of quantitative trait loci.
    Yang J; Zhu W; Chen J; Zhang Q; Wu S
    BMC Genet; 2014 Feb; 15():20. PubMed ID: 24507412
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The effect of missing data on linkage disequilibrium mapping and haplotype association analysis in the GAW14 simulated datasets.
    McCaskie PA; Carter KW; McCaskie SR; Palmer LJ
    BMC Genet; 2005 Dec; 6 Suppl 1(Suppl 1):S151. PubMed ID: 16451612
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Designing genome-wide association studies: sample size, power, imputation, and the choice of genotyping chip.
    Spencer CC; Su Z; Donnelly P; Marchini J
    PLoS Genet; 2009 May; 5(5):e1000477. PubMed ID: 19492015
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Fast and robust association tests for untyped SNPs in case-control studies.
    Allen AS; Satten GA; Bray SL; Dudbridge F; Epstein MP
    Hum Hered; 2010; 70(3):167-76. PubMed ID: 20689309
    [TBL] [Abstract][Full Text] [Related]  

  • 14. KELVIN: a software package for rigorous measurement of statistical evidence in human genetics.
    Vieland VJ; Huang Y; Seok SC; Burian J; Catalyurek U; O'Connell J; Segre A; Valentine-Cooper W
    Hum Hered; 2011; 72(4):276-88. PubMed ID: 22189470
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel bayesian graphical model for genome-wide multi-SNP association mapping.
    Zhang Y
    Genet Epidemiol; 2012 Jan; 36(1):36-47. PubMed ID: 22127647
    [TBL] [Abstract][Full Text] [Related]  

  • 16. sim1000G: a user-friendly genetic variant simulator in R for unrelated individuals and family-based designs.
    Dimitromanolakis A; Xu J; Krol A; Briollais L
    BMC Bioinformatics; 2019 Jan; 20(1):26. PubMed ID: 30646839
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Design considerations for genetic linkage and association studies.
    Nsengimana J; Bishop DT
    Methods Mol Biol; 2012; 850():237-62. PubMed ID: 22307702
    [TBL] [Abstract][Full Text] [Related]  

  • 18. varLD: a program for quantifying variation in linkage disequilibrium patterns between populations.
    Ong RT; Teo YY
    Bioinformatics; 2010 May; 26(9):1269-70. PubMed ID: 20308177
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lep-MAP3: robust linkage mapping even for low-coverage whole genome sequencing data.
    Rastas P
    Bioinformatics; 2017 Dec; 33(23):3726-3732. PubMed ID: 29036272
    [TBL] [Abstract][Full Text] [Related]  

  • 20. GENEHUNTER: your 'one-stop shop' for statistical genetic analysis?
    Nyholt DR
    Hum Hered; 2002; 53(1):2-7. PubMed ID: 11901265
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.