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 *

105 related articles for article (PubMed ID: 29342236)

  • 1. MAGNAMWAR: an R package for genome-wide association studies of bacterial orthologs.
    Sexton CE; Smith HZ; Newell PD; Douglas AE; Chaston JM
    Bioinformatics; 2018 Jun; 34(11):1951-1952. PubMed ID: 29342236
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Hogwash: three methods for genome-wide association studies in bacteria.
    Saund K; Snitkin ES
    Microb Genom; 2020 Nov; 6(11):. PubMed ID: 33206035
    [TBL] [Abstract][Full Text] [Related]  

  • 3. repfdr: a tool for replicability analysis for genome-wide association studies.
    Heller R; Yaacoby S; Yekutieli D
    Bioinformatics; 2014 Oct; 30(20):2971-2. PubMed ID: 25012182
    [TBL] [Abstract][Full Text] [Related]  

  • 4. MultiMeta: an R package for meta-analyzing multi-phenotype genome-wide association studies.
    Vuckovic D; Gasparini P; Soranzo N; Iotchkova V
    Bioinformatics; 2015 Aug; 31(16):2754-6. PubMed ID: 25908790
    [TBL] [Abstract][Full Text] [Related]  

  • 5. NAM: association studies in multiple populations.
    Xavier A; Xu S; Muir WM; Rainey KM
    Bioinformatics; 2015 Dec; 31(23):3862-4. PubMed ID: 26243017
    [TBL] [Abstract][Full Text] [Related]  

  • 6. GAPIT: genome association and prediction integrated tool.
    Lipka AE; Tian F; Wang Q; Peiffer J; Li M; Bradbury PJ; Gore MA; Buckler ES; Zhang Z
    Bioinformatics; 2012 Sep; 28(18):2397-9. PubMed ID: 22796960
    [TBL] [Abstract][Full Text] [Related]  

  • 7. CASMAP: detection of statistically significant combinations of SNPs in association mapping.
    Llinares-López F; Papaxanthos L; Roqueiro D; Bodenham D; Borgwardt K
    Bioinformatics; 2019 Aug; 35(15):2680-2682. PubMed ID: 30541062
    [TBL] [Abstract][Full Text] [Related]  

  • 8. GWAF: an R package for genome-wide association analyses with family data.
    Chen MH; Yang Q
    Bioinformatics; 2010 Feb; 26(4):580-1. PubMed ID: 20040588
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Multiple testing in genome-wide association studies via hidden Markov models.
    Wei Z; Sun W; Wang K; Hakonarson H
    Bioinformatics; 2009 Nov; 25(21):2802-8. PubMed ID: 19654115
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The advent of genome-wide association studies for bacteria.
    Chen PE; Shapiro BJ
    Curr Opin Microbiol; 2015 Jun; 25():17-24. PubMed ID: 25835153
    [TBL] [Abstract][Full Text] [Related]  

  • 11. snpGeneSets: An R Package for Genome-Wide Study Annotation.
    Mei H; Li L; Jiang F; Simino J; Griswold M; Mosley T; Liu S
    G3 (Bethesda); 2016 Dec; 6(12):4087-4095. PubMed ID: 27807048
    [TBL] [Abstract][Full Text] [Related]  

  • 12. lodGWAS: a software package for genome-wide association analysis of biomarkers with a limit of detection.
    Vaez A; van der Most PJ; Prins BP; Snieder H; van den Heuvel E; Alizadeh BZ; Nolte IM
    Bioinformatics; 2016 May; 32(10):1552-4. PubMed ID: 26803157
    [TBL] [Abstract][Full Text] [Related]  

  • 13. cgmisc: enhanced genome-wide association analyses and visualization.
    Kierczak M; Jabłońska J; Forsberg SK; Bianchi M; Tengvall K; Pettersson M; Scholz V; Meadows JR; Jern P; Carlborg Ö; Lindblad-Toh K
    Bioinformatics; 2015 Dec; 31(23):3830-1. PubMed ID: 26249815
    [TBL] [Abstract][Full Text] [Related]  

  • 14. SECA: SNP effect concordance analysis using genome-wide association summary results.
    Nyholt DR
    Bioinformatics; 2014 Jul; 30(14):2086-8. PubMed ID: 24695403
    [TBL] [Abstract][Full Text] [Related]  

  • 15. traseR: an R package for performing trait-associated SNP enrichment analysis in genomic intervals.
    Chen L; Qin ZS
    Bioinformatics; 2016 Apr; 32(8):1214-6. PubMed ID: 26685307
    [TBL] [Abstract][Full Text] [Related]  

  • 16. ProbABEL package for genome-wide association analysis of imputed data.
    Aulchenko YS; Struchalin MV; van Duijn CM
    BMC Bioinformatics; 2010 Mar; 11():134. PubMed ID: 20233392
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Fast computation for genome-wide association studies using boosted one-step statistics.
    Voorman A; Rice K; Lumley T
    Bioinformatics; 2012 Jul; 28(14):1818-22. PubMed ID: 22592383
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The SNPMaP package for R: a framework for genome-wide association using DNA pooling on microarrays.
    Davis OS; Plomin R; Schalkwyk LC
    Bioinformatics; 2009 Jan; 25(2):281-3. PubMed ID: 19008252
    [TBL] [Abstract][Full Text] [Related]  

  • 19. CollapsABEL: an R library for detecting compound heterozygote alleles in genome-wide association studies.
    Zhong K; Karssen LC; Kayser M; Liu F
    BMC Bioinformatics; 2016 Apr; 17():156. PubMed ID: 27059780
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CGene: an R package for implementation of causal genetic analyses.
    Lipman PJ; Lange C
    Eur J Hum Genet; 2011 Dec; 19(12):1292-4. PubMed ID: 21731061
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.