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 *

121 related articles for article (PubMed ID: 27980665)

  • 1. Identifying rare and common variants with Bayesian variable selection.
    Oh C
    BMC Proc; 2016; 10(Suppl 7):379-384. PubMed ID: 27980665
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identifying rare variants using a Bayesian regression approach.
    Yan A; Laird NM; Li C
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S99. PubMed ID: 22373362
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Part 1. Statistical Learning Methods for the Effects of Multiple Air Pollution Constituents.
    Coull BA; Bobb JF; Wellenius GA; Kioumourtzoglou MA; Mittleman MA; Koutrakis P; Godleski JJ
    Res Rep Health Eff Inst; 2015 Jun; (183 Pt 1-2):5-50. PubMed ID: 26333238
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A robust GWSS method to simultaneously detect rare and common variants for complex disease.
    Kao CF; Liu JR; Hung H; Kuo PH
    PLoS One; 2015; 10(4):e0120873. PubMed ID: 25880329
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A comprehensive evaluation of collapsing methods using simulated and real data: excellent annotation of functionality and large sample sizes required.
    Dering C; König IR; Ramsey LB; Relling MV; Yang W; Ziegler A
    Front Genet; 2014; 5():323. PubMed ID: 25309579
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Combining effects from rare and common genetic variants in an exome-wide association study of sequence data.
    Aschard H; Qiu W; Pasaniuc B; Zaitlen N; Cho MH; Carey V
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S44. PubMed ID: 22373328
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Analysis of human mini-exome sequencing data from Genetic Analysis Workshop 17 using a Bayesian hierarchical mixture model.
    Bueno Filho JS; Morota G; Tran Q; Maenner MJ; Vera-Cala LM; Engelman CD; Meyers KJ
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S93. PubMed ID: 22373180
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evaluation of logistic Bayesian LASSO for identifying association with rare haplotypes.
    Biswas S; Papachristou C
    BMC Proc; 2014; 8(Suppl 1):S54. PubMed ID: 25519334
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Association of
    Bryant TS; Duggal P; Yu B; Morrison AC; Shafi T; Ehret G; Franceschini N; Boerwinkle E; Coresh J; Tin A
    Int J Hypertens; 2019; 2019():2137629. PubMed ID: 30906589
    [No Abstract]   [Full Text] [Related]  

  • 10. Evaluation of gene-based association tests for analyzing rare variants using Genetic Analysis Workshop 18 data.
    Derkach A; Lawless JF; Merico D; Paterson AD; Sun L
    BMC Proc; 2014; 8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S9. PubMed ID: 25519417
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Bivariate quantitative Bayesian LASSO for detecting association of rare haplotypes with two correlated continuous phenotypes.
    Sajal IH; Biswas S
    Front Genet; 2023; 14():1104727. PubMed ID: 36968609
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Digging into the extremes: a useful approach for the analysis of rare variants with continuous traits?
    Lamina C
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S105. PubMed ID: 22373517
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Pooled-DNA Sequencing for Elucidating New Genomic Risk Factors, Rare Variants Underlying Alzheimer's Disease.
    Jin SC; Benitez BA; Deming Y; Cruchaga C
    Methods Mol Biol; 2016; 1303():299-314. PubMed ID: 26235075
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Post hoc Analysis for Detecting Individual Rare Variant Risk Associations Using Probit Regression Bayesian Variable Selection Methods in Case-Control Sequencing Studies.
    Larson NB; McDonnell S; Albright LC; Teerlink C; Stanford J; Ostrander EA; Isaacs WB; Xu J; Cooney KA; Lange E; Schleutker J; Carpten JD; Powell I; Bailey-Wilson J; Cussenot O; Cancel-Tassin G; Giles G; MacInnis R; Maier C; Whittemore AS; Hsieh CL; Wiklund F; Catalona WJ; Foulkes W; Mandal D; Eeles R; Kote-Jarai Z; Ackerman MJ; Olson TM; Klein CJ; Thibodeau SN; Schaid DJ
    Genet Epidemiol; 2016 Sep; 40(6):461-9. PubMed ID: 27312771
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Variational inference for rare variant detection in deep, heterogeneous next-generation sequencing data.
    Zhang F; Flaherty P
    BMC Bioinformatics; 2017 Jan; 18(1):45. PubMed ID: 28103803
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identifying rare disease variants in the Genetic Analysis Workshop 17 simulated data: a comparison of several statistical approaches.
    Fan R; Huang CH; Lo SH; Zheng T; Ionita-Laza I
    BMC Proc; 2011; 5 Suppl 9(Suppl 9):S17. PubMed ID: 22373071
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide joint analysis of single-nucleotide variant sets and gene expression for hypertension and related phenotypes.
    Tong X; Wei C; Lu Q
    BMC Proc; 2016; 10(Suppl 7):125-129. PubMed ID: 27980623
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Meta-Qtest: meta-analysis of quadratic test for rare variants.
    Ka J; Lee J; Kim Y; Oh B; ; Park T
    BMC Med Genomics; 2019 Jul; 12(Suppl 5):102. PubMed ID: 31296221
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Detecting the Common and Individual Effects of Rare Variants on Quantitative Traits by Using Extreme Phenotype Sampling.
    Zhou YJ; Wang Y; Chen LL
    Genes (Basel); 2016 Jan; 7(1):. PubMed ID: 26784232
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Rare variant association test with multiple phenotypes.
    Lee S; Won S; Kim YJ; Kim Y; ; Kim BJ; Park T
    Genet Epidemiol; 2017 Apr; 41(3):198-209. PubMed ID: 28039885
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.