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 *

67 related articles for article (PubMed ID: 27346615)

  • 1. Context and Applications of Targeted Genetic Testing, with Emphasis on Copy Number Variants.
    Ahn JW; Ogilvie C
    Adv Clin Chem; 2016; 75():33-51. PubMed ID: 27346615
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The impact of human copy number variation on a new era of genetic testing.
    Choy KW; Setlur SR; Lee C; Lau TK
    BJOG; 2010 Mar; 117(4):391-8. PubMed ID: 20105165
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Application of Nexus copy number software for CNV detection and analysis.
    Darvishi K
    Curr Protoc Hum Genet; 2010 Apr; Chapter 4():Unit 4.14.1-28. PubMed ID: 20373515
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The impact of human copy number variation on gene expression.
    Gamazon ER; Stranger BE
    Brief Funct Genomics; 2015 Sep; 14(5):352-7. PubMed ID: 25922366
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Family-Based Benchmarking of Copy Number Variation Detection Software.
    Nutsua ME; Fischer A; Nebel A; Hofmann S; Schreiber S; Krawczak M; Nothnagel M
    PLoS One; 2015; 10(7):e0133465. PubMed ID: 26197066
    [TBL] [Abstract][Full Text] [Related]  

  • 6. No association between general cognitive ability and rare copy number variation.
    McRae AF; Wright MJ; Hansell NK; Montgomery GW; Martin NG
    Behav Genet; 2013 May; 43(3):202-7. PubMed ID: 23417127
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Diagnosis of copy number variation by Illumina next generation sequencing is comparable in performance to oligonucleotide array comparative genomic hybridisation.
    Hayes JL; Tzika A; Thygesen H; Berri S; Wood HM; Hewitt S; Pendlebury M; Coates A; Willoughby L; Watson CM; Rabbitts P; Roberts P; Taylor GR
    Genomics; 2013 Sep; 102(3):174-81. PubMed ID: 23598253
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Detection of copy number variation using SNP genotyping.
    Cooper GM; Mefford HC
    Methods Mol Biol; 2011; 767():243-52. PubMed ID: 21822880
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evaluation of the efficacy of constitutional array-based comparative genomic hybridization in the diagnosis of aneuploidy using genomic and amplified DNA.
    Tan NH; Palmer R; Wang R
    J Obstet Gynaecol Res; 2010 Feb; 36(1):19-26. PubMed ID: 20178523
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.
    Saadati HR; Wittig M; Helbig I; Häsler R; Anderson CA; Mathew CG; Kupcinskas L; Parkes M; Karlsen TH; Rosenstiel P; Schreiber S; Franke A
    BMC Med Genet; 2016 Apr; 17():26. PubMed ID: 27037036
    [TBL] [Abstract][Full Text] [Related]  

  • 11. CNVinspector: a web-based tool for the interactive evaluation of copy number variations in single patients and in cohorts.
    Knierim E; Schwarz JM; Schuelke M; Seelow D
    J Med Genet; 2013 Aug; 50(8):529-33. PubMed ID: 23729504
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Progress from genome-wide association studies and copy number variant studies in epilepsy.
    Leu C; Coppola A; Sisodiya SM
    Curr Opin Neurol; 2016 Apr; 29(2):158-67. PubMed ID: 26886358
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genome-wide high-resolution screening in Dupuytren's disease reveals common regions of DNA copy number alterations.
    Shih BB; Tassabehji M; Watson JS; McGrouther AD; Bayat A
    J Hand Surg Am; 2010 Jul; 35(7):1172-1183.e7. PubMed ID: 20561756
    [TBL] [Abstract][Full Text] [Related]  

  • 14. COKGEN: a software for the identification of rare copy number variation from SNP microarrays.
    Yavaş G; Koyutürk M; Ozsoyoğlu M; Gould MP; Laframboise T
    Pac Symp Biocomput; 2010; ():371-82. PubMed ID: 19908389
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recent advances in array comparative genomic hybridization technologies and their applications in human genetics.
    Lockwood WW; Chari R; Chi B; Lam WL
    Eur J Hum Genet; 2006 Feb; 14(2):139-48. PubMed ID: 16288307
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype copy number variations using Gaussian mixture models: theory and algorithms.
    Lin CY; Lo Y; Ye KQ
    Stat Appl Genet Mol Biol; 2012 Oct; 11(5):5. PubMed ID: 23079517
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Detection and interpretation of genomic structural variation in health and disease.
    Vandeweyer G; Kooy RF
    Expert Rev Mol Diagn; 2013 Jan; 13(1):61-82. PubMed ID: 23256704
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Copy number variation and autism: new insights and clinical implications.
    Chung BH; Tao VQ; Tso WW
    J Formos Med Assoc; 2014 Jul; 113(7):400-8. PubMed ID: 24961180
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Characterization of copy number variation in genomic regions containing STR loci using array comparative genomic hybridization.
    Repnikova EA; Rosenfeld JA; Bailes A; Weber C; Erdman L; McKinney A; Ramsey S; Hashimoto S; Lamb Thrush D; Astbury C; Reshmi SC; Shaffer LG; Gastier-Foster JM; Pyatt RE
    Forensic Sci Int Genet; 2013 Sep; 7(5):475-81. PubMed ID: 23948316
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Chromosome microarrays in diagnostic testing: interpreting the genomic data.
    Peters GB; Pertile MD
    Methods Mol Biol; 2014; 1168():117-55. PubMed ID: 24870134
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.