BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

353 related articles for article (PubMed ID: 19908389)

  • 1. 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]  

  • 2. Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans.
    Haraksingh RR; Abyzov A; Urban AE
    BMC Genomics; 2017 Apr; 18(1):321. PubMed ID: 28438122
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evaluation of copy number variation detection for a SNP array platform.
    Zhang X; Du R; Li S; Zhang F; Jin L; Wang H
    BMC Bioinformatics; 2014 Feb; 15():50. PubMed ID: 24555668
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Exploiting sequence similarity to validate the sensitivity of SNP arrays in detecting fine-scaled copy number variations.
    Wong G; Leckie C; Gorringe KL; Haviv I; Campbell IG; Kowalczyk A
    Bioinformatics; 2010 Apr; 26(8):1007-14. PubMed ID: 20189937
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An optimization framework for unsupervised identification of rare copy number variation from SNP array data.
    Yavas G; Koyutürk M; Ozsoyoğlu M; Gould MP; LaFramboise T
    Genome Biol; 2009; 10(10):R119. PubMed ID: 19849861
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.
    Komura D; Shen F; Ishikawa S; Fitch KR; Chen W; Zhang J; Liu G; Ihara S; Nakamura H; Hurles ME; Lee C; Scherer SW; Jones KW; Shapero MH; Huang J; Aburatani H
    Genome Res; 2006 Dec; 16(12):1575-84. PubMed ID: 17122084
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. A multi-array multi-SNP genotyping algorithm for Affymetrix SNP microarrays.
    Xiao Y; Segal MR; Yang YH; Yeh RF
    Bioinformatics; 2007 Jun; 23(12):1459-67. PubMed ID: 17459966
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.
    Lin CH; Huang MC; Li LH; Wu JY; Chen YT; Fann CS
    Hum Mutat; 2008 Aug; 29(8):1055-62. PubMed ID: 18470944
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
    Sokolowski M; Wasserman J; Wasserman D
    PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Copy number variations identified in the chicken using a 60K SNP BeadChip.
    Jia X; Chen S; Zhou H; Li D; Liu W; Yang N
    Anim Genet; 2013 Jun; 44(3):276-84. PubMed ID: 23173786
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Genome-wide algorithm for detecting CNV associations with diseases.
    Xu Y; Peng B; Fu Y; Amos CI
    BMC Bioinformatics; 2011 Aug; 12():331. PubMed ID: 21827692
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform.
    Eckel-Passow JE; Atkinson EJ; Maharjan S; Kardia SL; de Andrade M
    BMC Bioinformatics; 2011 May; 12():220. PubMed ID: 21627824
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Accuracy of CNV Detection from GWAS Data.
    Zhang D; Qian Y; Akula N; Alliey-Rodriguez N; Tang J; ; Gershon ES; Liu C
    PLoS One; 2011 Jan; 6(1):e14511. PubMed ID: 21249187
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A genome-wide scan for copy number variations using high-density single nucleotide polymorphism array in Simmental cattle.
    Wu Y; Fan H; Jing S; Xia J; Chen Y; Zhang L; Gao X; Li J; Gao H; Ren H
    Anim Genet; 2015 Jun; 46(3):289-98. PubMed ID: 25917301
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Modeling genetic inheritance of copy number variations.
    Wang K; Chen Z; Tadesse MG; Glessner J; Grant SF; Hakonarson H; Bucan M; Li M
    Nucleic Acids Res; 2008 Dec; 36(21):e138. PubMed ID: 18832372
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Detection and characterization of copy number variation in autism spectrum disorder.
    Marshall CR; Scherer SW
    Methods Mol Biol; 2012; 838():115-35. PubMed ID: 22228009
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.