BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 20078226)

  • 1. Stationary wavelet packet transform and dependent laplacian bivariate shrinkage estimator for array-CGH data smoothing.
    Nguyen N; Huang H; Oraintara S; Vo A
    J Comput Biol; 2010 Feb; 17(2):139-52. PubMed ID: 20078226
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Array CGH data modeling and smoothing in Stationary Wavelet Packet Transform domain.
    Huang H; Nguyen N; Oraintara S; Vo A
    BMC Genomics; 2008 Sep; 9 Suppl 2(Suppl 2):S17. PubMed ID: 18831782
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Heavy-Tailed Noise Suppression and Derivative Wavelet Scalogram for Detecting DNA Copy Number Aberrations.
    Nha Nguyen ; An Vo ; Haibin Sun ; Heng Huang
    IEEE/ACM Trans Comput Biol Bioinform; 2018; 15(5):1625-1635. PubMed ID: 28692986
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A GC-wave correction algorithm that improves the analytical performance of aCGH.
    Leo A; Walker AM; Lebo MS; Hendrickson B; Scholl T; Akmaev VR
    J Mol Diagn; 2012 Nov; 14(6):550-9. PubMed ID: 22922130
    [TBL] [Abstract][Full Text] [Related]  

  • 5. WaveDec: A Wavelet Approach to Identify Both Shared and Individual Patterns of Copy-Number Variations.
    Cai H; Chen P; Chen J; Cai J; Song Y; Han G
    IEEE Trans Biomed Eng; 2018 Feb; 65(2):353-364. PubMed ID: 29346103
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Classification of array CGH data using smoothed logistic regression model.
    Huang J; Salim A; Lei K; O'Sullivan K; Pawitan Y
    Stat Med; 2009 Dec; 28(30):3798-810. PubMed ID: 19856275
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A very fast and accurate method for calling aberrations in array-CGH data.
    Benelli M; Marseglia G; Nannetti G; Paravidino R; Zara F; Bricarelli FD; Torricelli F; Magi A
    Biostatistics; 2010 Jul; 11(3):515-8. PubMed ID: 20207682
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hybrid algorithms for multiple change-point detection in biological sequences.
    Priyadarshana M; Polushina T; Sofronov G
    Adv Exp Med Biol; 2015; 823():41-61. PubMed ID: 25381101
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A shifting level model algorithm that identifies aberrations in array-CGH data.
    Magi A; Benelli M; Marseglia G; Nannetti G; Scordo MR; Torricelli F
    Biostatistics; 2010 Apr; 11(2):265-80. PubMed ID: 19948744
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Robust smoothing of quantitative genomic data using second-generation wavelets and bivariate shrinkage.
    Hatsuda H
    IEEE Trans Biomed Eng; 2012 Aug; 59(8):2099-102. PubMed ID: 22581128
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Array-based comparative genomic hybridization as a tool for analyzing the leukemia genome.
    Strefford JC; Parker H
    Methods Mol Biol; 2009; 538():151-77. PubMed ID: 19277573
    [TBL] [Abstract][Full Text] [Related]  

  • 13. VEGA: variational segmentation for copy number detection.
    Morganella S; Cerulo L; Viglietto G; Ceccarelli M
    Bioinformatics; 2010 Dec; 26(24):3020-7. PubMed ID: 20959380
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Multiple Break-Points Detection in Array CGH Data via the Cross-Entropy Method.
    Priyadarshana WJ; Sofronov G
    IEEE/ACM Trans Comput Biol Bioinform; 2015; 12(2):487-98. PubMed ID: 26357234
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A robust Correntropy-based method for analyzing multisample aCGH data.
    Mohammadi M; Hodtani GA; Yassi M
    Genomics; 2015 Nov; 106(5):257-64. PubMed ID: 26247398
    [TBL] [Abstract][Full Text] [Related]  

  • 16. MSMAD: a computationally efficient method for the analysis of noisy array CGH data.
    Budinska E; Gelnarova E; Schimek MG
    Bioinformatics; 2009 Mar; 25(6):703-13. PubMed ID: 19147666
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Zoom-in array comparative genomic hybridization (aCGH) to detect germline rearrangements in cancer susceptibility genes.
    Staaf J; Borg A
    Methods Mol Biol; 2010; 653():221-35. PubMed ID: 20721746
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Functional performance of aCGH design for clinical cytogenetics.
    Gambin T; Stankiewicz P; Sykulski M; Gambin A
    Comput Biol Med; 2013 Jul; 43(6):775-85. PubMed ID: 23668354
    [TBL] [Abstract][Full Text] [Related]  

  • 19. ADaCGH: A parallelized web-based application and R package for the analysis of aCGH data.
    Díaz-Uriarte R; Rueda OM
    PLoS One; 2007 Aug; 2(8):e737. PubMed ID: 17710137
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of DNA copy number aberrations associated with metastases of colorectal cancer using array CGH profiles.
    Nakao M; Kawauchi S; Furuya T; Uchiyama T; Adachi J; Okada T; Ikemoto K; Oga A; Sasaki K
    Cancer Genet Cytogenet; 2009 Jan; 188(2):70-6. PubMed ID: 19100508
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.