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 *

133 related articles for article (PubMed ID: 26954760)

  • 1. Sequential model selection-based segmentation to detect DNA copy number variation.
    Hu J; Zhang L; Wang HJ
    Biometrics; 2016 Sep; 72(3):815-26. PubMed ID: 26954760
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Detecting copy number variations from array CGH data based on a conditional random field model.
    Yin XL; Li J
    J Bioinform Comput Biol; 2010 Apr; 8(2):295-314. PubMed ID: 20401947
    [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. Joint segmentation, calling, and normalization of multiple CGH profiles.
    Picard F; Lebarbier E; Hoebeke M; Rigaill G; Thiam B; Robin S
    Biostatistics; 2011 Jul; 12(3):413-28. PubMed ID: 21209153
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of differential aberrations in multiple-sample array CGH studies.
    Wang HJ; Hu J
    Biometrics; 2011 Jun; 67(2):353-62. PubMed ID: 20618310
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fast Bayesian Inference of Copy Number Variants using Hidden Markov Models with Wavelet Compression.
    Wiedenhoeft J; Brugel E; Schliep A
    PLoS Comput Biol; 2016 May; 12(5):e1004871. PubMed ID: 27177143
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Genomic profiling of myeloma: the best approach, a comparison of cytogenetics, FISH and array-CGH of 112 myeloma cases.
    Rack K; Vidrequin S; Dargent JL
    J Clin Pathol; 2016 Jan; 69(1):82-6. PubMed ID: 26338801
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Modified screening and ranking algorithm for copy number variation detection.
    Xiao F; Min X; Zhang H
    Bioinformatics; 2015 May; 31(9):1341-8. PubMed ID: 25542927
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 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. Comparative genomic hybridization to detect variation in the copy number of large DNA segments.
    Holcomb IN; Trask BJ
    Cold Spring Harb Protoc; 2011 Nov; 2011(11):1323-33. PubMed ID: 22046040
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A statistical approach for array CGH data analysis.
    Picard F; Robin S; Lavielle M; Vaisse C; Daudin JJ
    BMC Bioinformatics; 2005 Feb; 6():27. PubMed ID: 15705208
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Simple binary segmentation frameworks for identifying variation in DNA copy number.
    Yang TY
    BMC Bioinformatics; 2012 Oct; 13():277. PubMed ID: 23107320
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A latent class model with hidden Markov dependence for array CGH data.
    DeSantis SM; Houseman EA; Coull BA; Louis DN; Mohapatra G; Betensky RA
    Biometrics; 2009 Dec; 65(4):1296-305. PubMed ID: 19397578
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Bayesian Random Segmentation Models to Identify Shared Copy Number Aberrations for Array CGH Data.
    Baladandayuthapani V; Ji Y; Talluri R; Nieto-Barajas LE; Morris JS
    J Am Stat Assoc; 2010 Dec; 105(492):1358-1375. PubMed ID: 21512611
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A comparative genomic hybridization approach to study gene copy number variations among Chinese hamster cell lines.
    Vishwanathan N; Bandyopadhyay A; Fu HY; Johnson KC; Springer NM; Hu WS
    Biotechnol Bioeng; 2017 Aug; 114(8):1903-1908. PubMed ID: 28409824
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Post-selection inference for changepoint detection algorithms with application to copy number variation data.
    Hyun S; Lin KZ; G'Sell M; Tibshirani RJ
    Biometrics; 2021 Sep; 77(3):1037-1049. PubMed ID: 33434289
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.