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 *

204 related articles for article (PubMed ID: 26306642)

  • 21. Analyses and comparison of accuracy of different genotype imputation methods.
    Pei YF; Li J; Zhang L; Papasian CJ; Deng HW
    PLoS One; 2008; 3(10):e3551. PubMed ID: 18958166
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing.
    Howie B; Fuchsberger C; Stephens M; Marchini J; Abecasis GR
    Nat Genet; 2012 Jul; 44(8):955-9. PubMed ID: 22820512
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A Unifying Framework for Imputing Summary Statistics in Genome-Wide Association Studies.
    Wu Y; Eskin E; Sankararaman S
    J Comput Biol; 2020 Mar; 27(3):418-428. PubMed ID: 32053016
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Systematic assessment of imputation performance using the 1000 Genomes reference panels.
    Liu Q; Cirulli ET; Han Y; Yao S; Liu S; Zhu Q
    Brief Bioinform; 2015 Jul; 16(4):549-62. PubMed ID: 25246238
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The predictive capacity of polygenic risk scores for disease risk is only moderately influenced by imputation panels tailored to the target population.
    Levi H; Elkon R; Shamir R
    Bioinformatics; 2024 Feb; 40(2):. PubMed ID: 38265251
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Adapt-Mix: learning local genetic correlation structure improves summary statistics-based analyses.
    Park DS; Brown B; Eng C; Huntsman S; Hu D; Torgerson DG; Burchard EG; Zaitlen N
    Bioinformatics; 2015 Jun; 31(12):i181-9. PubMed ID: 26072481
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Analysis of untyped SNPs: maximum likelihood and imputation methods.
    Hu YJ; Lin DY
    Genet Epidemiol; 2010 Dec; 34(8):803-15. PubMed ID: 21104886
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Evaluation of vicinity-based hidden Markov models for genotype imputation.
    Wang S; Kim M; Jiang X; Harmanci AO
    BMC Bioinformatics; 2022 Aug; 23(1):356. PubMed ID: 36038834
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Effect of genome-wide genotyping and reference panels on rare variants imputation.
    Zheng HF; Ladouceur M; Greenwood CM; Richards JB
    J Genet Genomics; 2012 Oct; 39(10):545-50. PubMed ID: 23089364
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Iam hiQ-a novel pair of accuracy indices for imputed genotypes.
    Rosenberger A; Tozzi V; Bickeböller H;
    BMC Bioinformatics; 2022 Jan; 23(1):50. PubMed ID: 35073846
    [TBL] [Abstract][Full Text] [Related]  

  • 31. EagleImp: fast and accurate genome-wide phasing and imputation in a single tool.
    Wienbrandt L; Ellinghaus D
    Bioinformatics; 2022 Nov; 38(22):4999-5006. PubMed ID: 36130053
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Accurate and adaptive imputation of summary statistics in mixed-ethnicity cohorts.
    Togninalli M; Roqueiro D; ; Borgwardt KM
    Bioinformatics; 2018 Sep; 34(17):i687-i696. PubMed ID: 30423082
    [TBL] [Abstract][Full Text] [Related]  

  • 33. IGG3: a tool to rapidly integrate large genotype datasets for whole-genome imputation and individual-level meta-analysis.
    Li MX; Jiang L; Kao PY; Sham PC; Song YQ
    Bioinformatics; 2009 Jun; 25(11):1449-50. PubMed ID: 19346322
    [TBL] [Abstract][Full Text] [Related]  

  • 34. GACT: a Genome build and Allele definition Conversion Tool for SNP imputation and meta-analysis in genetic association studies.
    Sulovari A; Li D
    BMC Genomics; 2014 Jul; 15():610. PubMed ID: 25038819
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Revisit Population-based and Family-based Genotype Imputation.
    Liu CT; Deng X; Fisher V; Heard-Costa N; Xu H; Zhou Y; Vasan RS; Cupples LA
    Sci Rep; 2019 Feb; 9(1):1800. PubMed ID: 30755687
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Strategies for Imputing and Analyzing Rare Variants in Association Studies.
    Hoffmann TJ; Witte JS
    Trends Genet; 2015 Oct; 31(10):556-563. PubMed ID: 26450338
    [TBL] [Abstract][Full Text] [Related]  

  • 38. HapBoost: a fast approach to boosting haplotype association analyses in genome-wide association studies.
    Wan X; Yang C; Yang Q; Zhao H; Yu W
    IEEE/ACM Trans Comput Biol Bioinform; 2013; 10(1):207-12. PubMed ID: 23702557
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Multi-ethnic Imputation System (MI-System): A genotype imputation server for high-dimensional data.
    Chattopadhyay A; Lee CY; Shen YC; Lu KC; Hsiao TH; Lin CH; Lai LC; Tsai MH; Lu TP; Chuang EY
    J Biomed Inform; 2023 Jul; 143():104423. PubMed ID: 37308034
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Accuracy of genotype imputation in sheep breeds.
    Hayes BJ; Bowman PJ; Daetwyler HD; Kijas JW; van der Werf JH
    Anim Genet; 2012 Feb; 43(1):72-80. PubMed ID: 22221027
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.