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 *

103 related articles for article (PubMed ID: 25381101)

  • 1. 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]  

  • 2. 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]  

  • 3. Multisample aCGH data analysis via total variation and spectral regularization.
    Zhou X; Yang C; Wan X; Zhao H; Yu W
    IEEE/ACM Trans Comput Biol Bioinform; 2013; 10(1):230-5. PubMed ID: 23702561
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation.
    Karimpour-Fard A; Dumas L; Phang T; Sikela JM; Hunter LE
    Hum Genomics; 2010 Aug; 4(6):421-7. PubMed ID: 20846932
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. An Entropy-Regularized Framework for Detecting Copy Number Variants.
    Mohammadi M; Farahi F
    IEEE Trans Biomed Eng; 2019 Mar; 66(3):682-688. PubMed ID: 29993514
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Optimization of Signal Decomposition Matched Filtering (SDMF) for Improved Detection of Copy-Number Variations.
    Stamoulis C; Betensky RA
    IEEE/ACM Trans Comput Biol Bioinform; 2016; 13(3):584-91. PubMed ID: 27295643
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A statistical change point model approach for the detection of DNA copy number variations in array CGH data.
    Chen J; Wang YP
    IEEE/ACM Trans Comput Biol Bioinform; 2009; 6(4):529-41. PubMed ID: 19875853
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DNA Copy Number Selection Using Robust Structured Sparsity-Inducing Norms.
    Metsis V; Makedon F; Shen D; Huang H
    IEEE/ACM Trans Comput Biol Bioinform; 2014; 11(1):168-81. PubMed ID: 26355516
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Modeling the DNA copy number aberration patterns in observational high-throughput cancer data.
    van Wieringen WN; Roś BP; Wilting SM
    Stat Appl Genet Mol Biol; 2013 Apr; 12(2):143-74. PubMed ID: 23735435
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. A Projection Neural Network for Identifying Copy Number Variants.
    Mohammadi M; Mansoori A
    IEEE J Biomed Health Inform; 2019 Sep; 23(5):2182-2188. PubMed ID: 30235154
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Penalized weighted low-rank approximation for robust recovery of recurrent copy number variations.
    Gao X
    BMC Bioinformatics; 2015 Dec; 16():407. PubMed ID: 26652207
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Experimental designs for array comparative genomic hybridization technology.
    McDonnell SK; Riska SM; Klee EW; Thorland EC; Kay NE; Thibodeau SN; Parker AS; Eckel-Passow JE
    Cytogenet Genome Res; 2013; 139(4):250-7. PubMed ID: 23548696
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.