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 *

114 related articles for article (PubMed ID: 22694346)

  • 1. Bayesian model to detect phenotype-specific genes for copy number data.
    González JR; Abellán C; Abellán JJ
    BMC Bioinformatics; 2012 Jun; 13():130. PubMed ID: 22694346
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Copy number variation detection in whole-genome sequencing data using the Bayesian information criterion.
    Xi R; Hadjipanayis AG; Luquette LJ; Kim TM; Lee E; Zhang J; Johnson MD; Muzny DM; Wheeler DA; Gibbs RA; Kucherlapati R; Park PJ
    Proc Natl Acad Sci U S A; 2011 Nov; 108(46):E1128-36. PubMed ID: 22065754
    [TBL] [Abstract][Full Text] [Related]  

  • 3. POPSTR: Inference of Admixed Population Structure Based on Single-Nucleotide Polymorphisms and Copy Number Variations.
    Ahn J; Conkright B; Boca SM; Madhavan S
    J Comput Biol; 2018 Apr; 25(4):417-429. PubMed ID: 29293371
    [TBL] [Abstract][Full Text] [Related]  

  • 4. CNVassoc: Association analysis of CNV data using R.
    Subirana I; Diaz-Uriarte R; Lucas G; Gonzalez JR
    BMC Med Genomics; 2011 May; 4():47. PubMed ID: 21609482
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Copy-number variation and association studies of human disease.
    McCarroll SA; Altshuler DM
    Nat Genet; 2007 Jul; 39(7 Suppl):S37-42. PubMed ID: 17597780
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Accounting for uncertainty when assessing association between copy number and disease: a latent class model.
    González JR; Subirana I; Escaramís G; Peraza S; Cáceres A; Estivill X; Armengol L
    BMC Bioinformatics; 2009 Jun; 10():172. PubMed ID: 19500389
    [TBL] [Abstract][Full Text] [Related]  

  • 7. FunVar: A systematic pipeline to unravel the convergence patterns of genetic variants in ASD, a paradigmatic complex disease.
    Asif M; Vicente AM; Couto FM
    J Biomed Inform; 2019 Oct; 98():103273. PubMed ID: 31454647
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Empirical Bayes screening of many p-values with applications to microarray studies.
    Datta S; Datta S
    Bioinformatics; 2005 May; 21(9):1987-94. PubMed ID: 15691856
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Segmentation and estimation for SNP microarrays: a Bayesian multiple change-point approach.
    Tai YC; Kvale MN; Witte JS
    Biometrics; 2010 Sep; 66(3):675-83. PubMed ID: 19764955
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Identification of copy number variants defining genomic differences among major human groups.
    Armengol L; Villatoro S; González JR; Pantano L; García-Aragonés M; Rabionet R; Cáceres M; Estivill X
    PLoS One; 2009 Sep; 4(9):e7230. PubMed ID: 19789632
    [TBL] [Abstract][Full Text] [Related]  

  • 11. On the frequency of copy number variants.
    Ionita-Laza I; Laird NM; Raby BA; Weiss ST; Lange C
    Bioinformatics; 2008 Oct; 24(20):2350-5. PubMed ID: 18689430
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A multilevel model to address batch effects in copy number estimation using SNP arrays.
    Scharpf RB; Ruczinski I; Carvalho B; Doan B; Chakravarti A; Irizarry RA
    Biostatistics; 2011 Jan; 12(1):33-50. PubMed ID: 20625178
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.
    Korn JM; Kuruvilla FG; McCarroll SA; Wysoker A; Nemesh J; Cawley S; Hubbell E; Veitch J; Collins PJ; Darvishi K; Lee C; Nizzari MM; Gabriel SB; Purcell S; Daly MJ; Altshuler D
    Nat Genet; 2008 Oct; 40(10):1253-60. PubMed ID: 18776909
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An integrative segmentation method for detecting germline copy number variations in SNP arrays.
    Shi J; Li P
    Genet Epidemiol; 2012 May; 36(4):373-83. PubMed ID: 22539397
    [TBL] [Abstract][Full Text] [Related]  

  • 15. PlatinumCNV: a Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data.
    Kumasaka N; Fujisawa H; Hosono N; Okada Y; Takahashi A; Nakamura Y; Kubo M; Kamatani N
    Genet Epidemiol; 2011 Dec; 35(8):831-44. PubMed ID: 22125222
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Concordance rate between copy number variants detected using either high- or medium-density single nucleotide polymorphism genotype panels and the potential of imputing copy number variants from flanking high density single nucleotide polymorphism haplotypes in cattle.
    Rafter P; Gormley IC; Parnell AC; Kearney JF; Berry DP
    BMC Genomics; 2020 Mar; 21(1):205. PubMed ID: 32131735
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.
    Estivill X; Armengol L
    PLoS Genet; 2007 Oct; 3(10):1787-99. PubMed ID: 17953491
    [TBL] [Abstract][Full Text] [Related]  

  • 18. High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function.
    Bestetti I; Castronovo C; Sironi A; Caslini C; Sala C; Rossetti R; Crippa M; Ferrari I; Pistocchi A; Toniolo D; Persani L; Marozzi A; Finelli P
    Hum Reprod; 2019 Mar; 34(3):574-583. PubMed ID: 30689869
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A Bayesian segmentation approach to ascertain copy number variations at the population level.
    Wu LY; Chipman HA; Bull SB; Briollais L; Wang K
    Bioinformatics; 2009 Jul; 25(13):1669-79. PubMed ID: 19389735
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Copy number polymorphisms in new HapMap III and Singapore populations.
    Ku CS; Teo SM; Naidoo N; Sim X; Teo YY; Pawitan Y; Seielstad M; Chia KS; Salim A
    J Hum Genet; 2011 Aug; 56(8):552-60. PubMed ID: 21677662
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.