BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 21989070)

  • 1. SNP and gene networks construction and analysis from classification of copy number variations data.
    Liu Y; Lee YF; Ng MK
    BMC Bioinformatics; 2011; 12 Suppl 5(Suppl 5):S4. PubMed ID: 21989070
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Shrunken methodology to genome-wide SNPs selection and construction of SNPs networks.
    Liu Y; Ng M
    BMC Syst Biol; 2010 Sep; 4 Suppl 2(Suppl 2):S5. PubMed ID: 20840732
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-wide analysis of copy number variation in type 1 diabetes.
    Grayson BL; Smith ME; Thomas JW; Wang L; Dexheimer P; Jeffrey J; Fain PR; Nanduri P; Eisenbarth GS; Aune TM
    PLoS One; 2010 Nov; 5(11):e15393. PubMed ID: 21085585
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Screening of lung cancer related SNPs and CNVs with SNP microarrays.
    Li TY; Zhang F
    Eur Rev Med Pharmacol Sci; 2015; 19(2):225-34. PubMed ID: 25683935
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Identification and validation of copy number variants using SNP genotyping arrays from a large clinical cohort.
    Valsesia A; Stevenson BJ; Waterworth D; Mooser V; Vollenweider P; Waeber G; Jongeneel CV; Beckmann JS; Kutalik Z; Bergmann S
    BMC Genomics; 2012 Jun; 13():241. PubMed ID: 22702538
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Cheek swabs, SNP chips, and CNVs: assessing the quality of copy number variant calls generated with subject-collected mail-in buccal brush DNA samples on a high-density genotyping microarray.
    Erickson SW; MacLeod SL; Hobbs CA
    BMC Med Genet; 2012 Jun; 13():51. PubMed ID: 22734463
    [TBL] [Abstract][Full Text] [Related]  

  • 9. CNVmap: A Method and Software To Detect and Map Copy Number Variants from Segregation Data.
    Falque M; Jebreen K; Paux E; Knaak C; Mezmouk S; Martin OC
    Genetics; 2020 Mar; 214(3):561-576. PubMed ID: 31882400
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits.
    da Silva JM; Giachetto PF; da Silva LO; Cintra LC; Paiva SR; Yamagishi ME; Caetano AR
    BMC Genomics; 2016 Jun; 17():454. PubMed ID: 27297173
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Genome-wide identification of copy number variations in Holstein cattle from Baja California, Mexico, using high-density SNP genotyping arrays.
    Salomón-Torres R; González-Vizcarra VM; Medina-Basulto GE; Montaño-Gómez MF; Mahadevan P; Yaurima-Basaldúa VH; Villa-Angulo C; Villa-Angulo R
    Genet Mol Res; 2015 Oct; 14(4):11848-59. PubMed ID: 26436509
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Copy number variations in Friesian horses and genetic risk factors for insect bite hypersensitivity.
    Schurink A; da Silva VH; Velie BD; Dibbits BW; Crooijmans RPMA; Franҫois L; Janssens S; Stinckens A; Blott S; Buys N; Lindgren G; Ducro BJ
    BMC Genet; 2018 Jul; 19(1):49. PubMed ID: 30060732
    [TBL] [Abstract][Full Text] [Related]  

  • 15. CONAN: copy number variation analysis software for genome-wide association studies.
    Forer L; Schönherr S; Weissensteiner H; Haider F; Kluckner T; Gieger C; Wichmann HE; Specht G; Kronenberg F; Kloss-Brandstätter A
    BMC Bioinformatics; 2010 Jun; 11():318. PubMed ID: 20546565
    [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. Whole genome resequencing of black Angus and Holstein cattle for SNP and CNV discovery.
    Stothard P; Choi JW; Basu U; Sumner-Thomson JM; Meng Y; Liao X; Moore SS
    BMC Genomics; 2011 Nov; 12():559. PubMed ID: 22085807
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
    Liu J; Zhou Y; Liu S; Song X; Yang XZ; Fan Y; Chen W; Akdemir ZC; Yan Z; Zuo Y; Du R; Liu Z; Yuan B; Zhao S; Liu G; Chen Y; Zhao Y; Lin M; Zhu Q; Niu Y; Liu P; Ikegawa S; Song YQ; Posey JE; Qiu G; ; Zhang F; Wu Z; Lupski JR; Wu N
    Hum Genet; 2018 Jul; 137(6-7):553-567. PubMed ID: 30019117
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel association strategy with copy number variation for identifying new risk Loci of human diseases.
    Chen X; Li X; Wang P; Liu Y; Zhang Z; Zhao G; Xu H; Zhu J; Qin X; Chen S; Hu L; Kong X
    PLoS One; 2010 Aug; 5(8):e12185. PubMed ID: 20808825
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients.
    Zhao L; Triche EW; Walsh KM; Bracken MB; Saftlas AF; Hoh J; Dewan AT
    BMC Pregnancy Childbirth; 2012 Jun; 12():61. PubMed ID: 22748001
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.