BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

316 related articles for article (PubMed ID: 22309429)

  • 1. Weighted selective collapsing strategy for detecting rare and common variants in genetic association study.
    Dai Y; Jiang R; Dong J
    BMC Genet; 2012 Feb; 13():7. PubMed ID: 22309429
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Improved power by collapsing rare and common variants based on a data-adaptive forward selection strategy.
    Dai Y; Guo L; Dong J; Jiang R
    BMC Proc; 2011 Nov; 5 Suppl 9(Suppl 9):S114. PubMed ID: 22373230
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A modified association test for rare and common variants based on affected sib-pair design.
    Guo Y; Zhou Y
    J Theor Biol; 2019 Apr; 467():1-6. PubMed ID: 30707975
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The power comparison of the haplotype-based collapsing tests and the variant-based collapsing tests for detecting rare variants in pedigrees.
    Guo W; Shugart YY
    BMC Genomics; 2014 Jul; 15(1):632. PubMed ID: 25070353
    [TBL] [Abstract][Full Text] [Related]  

  • 5. GENOME-WIDE ASSOCIATION MAPPING AND RARE ALLELES: FROM POPULATION GENOMICS TO PERSONALIZED MEDICINE - Session Introduction.
    DE LA Vega FM; Bustamante CD; Leal SM
    Pac Symp Biocomput; 2011; ():74-5. PubMed ID: 21121034
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identifying rare variants associated with complex traits via sequencing.
    Li B; Liu DJ; Leal SM
    Curr Protoc Hum Genet; 2013 Jul; Chapter 1():Unit 1.26. PubMed ID: 23853079
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Block-based association tests for rare variants using Kullback-Leibler divergence.
    Zhu D; Hu YQ; Lin S
    J Hum Genet; 2016 Nov; 61(11):965-975. PubMed ID: 27412875
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Powerful Pathway-Based Adaptive Test for Genetic Association with Common or Rare Variants.
    Pan W; Kwak IY; Wei P
    Am J Hum Genet; 2015 Jul; 97(1):86-98. PubMed ID: 26119817
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Pleiotropy informed adaptive association test of multiple traits using genome-wide association study summary data.
    Masotti M; Guo B; Wu B
    Biometrics; 2019 Dec; 75(4):1076-1085. PubMed ID: 31021400
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Utilizing mutual information for detecting rare and common variants associated with a categorical trait.
    Sun L; Wang C; Hu YQ
    PeerJ; 2016; 4():e2139. PubMed ID: 27350900
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Statistical selection strategy for risk and protective rare variants associated with complex traits.
    Kim S; Lee K; Sun H
    J Comput Biol; 2015 Nov; 22(11):1034-43. PubMed ID: 26469994
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A robust model-free approach for rare variants association studies incorporating gene-gene and gene-environmental interactions.
    Fan R; Lo SH
    PLoS One; 2013; 8(12):e83057. PubMed ID: 24358248
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Two-stage design of sequencing studies for testing association with rare variants.
    Yang F; Thomas DC
    Hum Hered; 2011; 71(4):209-20. PubMed ID: 21734405
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Integrate multiple traits to detect novel trait-gene association using GWAS summary data with an adaptive test approach.
    Guo B; Wu B
    Bioinformatics; 2019 Jul; 35(13):2251-2257. PubMed ID: 30476000
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Weighted pedigree-based statistics for testing the association of rare variants.
    Shugart YY; Zhu Y; Guo W; Xiong M
    BMC Genomics; 2012 Nov; 13():667. PubMed ID: 23176082
    [TBL] [Abstract][Full Text] [Related]  

  • 16. An optimum projection and noise reduction approach for detecting rare and common variants associated with complex diseases.
    Turkmen A; Lin S
    Hum Hered; 2012; 74(1):51-60. PubMed ID: 23154579
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detecting association of rare and common variants by adaptive combination of P-values.
    Zhou Y; Wang Y
    Genet Res (Camb); 2015 Oct; 97():e20. PubMed ID: 26440553
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel genome-information content-based statistic for genome-wide association analysis designed for next-generation sequencing data.
    Luo L; Zhu Y; Xiong M
    J Comput Biol; 2012 Jun; 19(6):731-44. PubMed ID: 22651812
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rare variant analysis for family-based design.
    De G; Yip WK; Ionita-Laza I; Laird N
    PLoS One; 2013; 8(1):e48495. PubMed ID: 23341868
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An adaptive strategy for association analysis of common or rare variants using entropy theory.
    Li YM; Xu C; Xiang Y; Peng C; Deng HW
    J Hum Genet; 2017 Aug; 62(8):777-781. PubMed ID: 28381878
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.