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 *

189 related articles for article (PubMed ID: 22929166)

  • 81. 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]  

  • 82. APE: Analyses of Phylogenetics and Evolution in R language.
    Paradis E; Claude J; Strimmer K
    Bioinformatics; 2004 Jan; 20(2):289-90. PubMed ID: 14734327
    [TBL] [Abstract][Full Text] [Related]  

  • 83. Mapping quantitative trait loci for binary trait in the F2:3 design.
    Zhu C; Zhang YM; Guo Z
    J Genet; 2008 Dec; 87(3):201-7. PubMed ID: 19147904
    [TBL] [Abstract][Full Text] [Related]  

  • 84. GOplot: an R package for visually combining expression data with functional analysis.
    Walter W; Sánchez-Cabo F; Ricote M
    Bioinformatics; 2015 Sep; 31(17):2912-4. PubMed ID: 25964631
    [TBL] [Abstract][Full Text] [Related]  

  • 85. TLINKAGE-IMPRINT: a model-based approach to performing two-locus genetic imprinting analysis.
    Shete S; Zhou X
    Hum Hered; 2006; 62(3):145-56. PubMed ID: 17057404
    [TBL] [Abstract][Full Text] [Related]  

  • 86. Robustness and power of the maximum-likelihood-binomial and maximum-likelihood-score methods, in multipoint linkage analysis of affected-sibship data.
    Abel L; Müller-Myhsok B
    Am J Hum Genet; 1998 Aug; 63(2):638-47. PubMed ID: 9683590
    [TBL] [Abstract][Full Text] [Related]  

  • 87. Maximum likelihood estimation of linkage between a marker gene and a quantitative locus.
    Luo ZW; Kearsey MJ
    Heredity (Edinb); 1989 Dec; 63 ( Pt 3)():401-8. PubMed ID: 2613536
    [TBL] [Abstract][Full Text] [Related]  

  • 88. Ravages: An R package for the simulation and analysis of rare variants in multicategory phenotypes.
    Bocher O; Marenne G; Génin E; Perdry H
    Genet Epidemiol; 2023 Sep; 47(6):450-460. PubMed ID: 37158367
    [TBL] [Abstract][Full Text] [Related]  

  • 89. Assessment and management of single nucleotide polymorphism genotype errors in genetic association analysis.
    Gordon D; Ott J
    Pac Symp Biocomput; 2001; ():18-29. PubMed ID: 11262939
    [TBL] [Abstract][Full Text] [Related]  

  • 90. Risks of cancer due to a single BRCA1 mutation in an extended Utah kindred.
    Vogl FD; Badzioch MD; Steele L; Neuhausen SL; Goldgar DE
    Fam Cancer; 2007; 6(1):63-71. PubMed ID: 17051349
    [TBL] [Abstract][Full Text] [Related]  

  • 91. Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relatives.
    Bureau A; Younkin SG; Parker MM; Bailey-Wilson JE; Marazita ML; Murray JC; Mangold E; Albacha-Hejazi H; Beaty TH; Ruczinski I
    Bioinformatics; 2014 Aug; 30(15):2189-96. PubMed ID: 24740360
    [TBL] [Abstract][Full Text] [Related]  

  • 92. Fast linkage analysis with MOD scores using algebraic calculation.
    Brugger M; Strauch K
    Hum Hered; 2014; 78(3-4):179-94. PubMed ID: 25633962
    [TBL] [Abstract][Full Text] [Related]  

  • 93. Genetic Analysis Workshop II: results of segregation analyses using POINTER and linkage analyses using LIPED.
    Cox NJ
    Genet Epidemiol; 1984; 1(2):167-70. PubMed ID: 14964297
    [TBL] [Abstract][Full Text] [Related]  

  • 94. Combining identity by descent and association in genetic case-control studies.
    Zhang Q; Wang S; Ott J
    BMC Genet; 2008 Jul; 9():42. PubMed ID: 18601744
    [TBL] [Abstract][Full Text] [Related]  

  • 95. Quantitative trait locus mapping using human pedigrees.
    Blangero J; Williams JT; Almasy L
    Hum Biol; 2000 Feb; 72(1):35-62. PubMed ID: 10721613
    [TBL] [Abstract][Full Text] [Related]  

  • 96. Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium.
    Easton DF; Bishop DT; Ford D; Crockford GP
    Am J Hum Genet; 1993 Apr; 52(4):678-701. PubMed ID: 8460634
    [TBL] [Abstract][Full Text] [Related]  

  • 97. Linkage analysis assuming a single-locus mode of inheritance for traits determined by two loci: inferring mode of inheritance and estimating penetrance.
    Greenberg DA
    Genet Epidemiol; 1990; 7(6):467-79. PubMed ID: 2292371
    [TBL] [Abstract][Full Text] [Related]  

  • 98. 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]  

  • 99. Maximum-likelihood estimation of recent shared ancestry (ERSA).
    Huff CD; Witherspoon DJ; Simonson TS; Xing J; Watkins WS; Zhang Y; Tuohy TM; Neklason DW; Burt RW; Guthery SL; Woodward SR; Jorde LB
    Genome Res; 2011 May; 21(5):768-74. PubMed ID: 21324875
    [TBL] [Abstract][Full Text] [Related]  

  • 100. PedGenie: meta genetic association testing in mixed family and case-control designs.
    Curtin K; Wong J; Allen-Brady K; Camp NJ
    BMC Bioinformatics; 2007 Nov; 8():448. PubMed ID: 18005446
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.