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 *

174 related articles for article (PubMed ID: 28692986)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Exploiting noise in array CGH data to improve detection of DNA copy number change.
    Hu J; Gao JB; Cao Y; Bottinger E; Zhang W
    Nucleic Acids Res; 2007; 35(5):e35. PubMed ID: 17272296
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The use of ultra-dense array CGH analysis for the discovery of micro-copy number alterations and gene fusions in the cancer genome.
    Przybytkowski E; Ferrario C; Basik M
    BMC Med Genomics; 2011 Jan; 4():16. PubMed ID: 21272361
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Comparative Genomic Hybridization (CGH) in Genotoxicology.
    Baumgartner A; Hartleb V; Taylor JD
    Methods Mol Biol; 2019; 2031():209-234. PubMed ID: 31473962
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Noise cancellation using total variation for copy number variation detection.
    Zare F; Hosny A; Nabavi S
    BMC Bioinformatics; 2018 Oct; 19(Suppl 11):361. PubMed ID: 30343665
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of De Novo and Rare Inherited Copy Number Variants in Children with Syndromic Congenital Heart Defects.
    Hussein IR; Bader RS; Chaudhary AG; Bassiouni R; Alquaiti M; Ashgan F; Schulten HJ; Al Qahtani MH
    Pediatr Cardiol; 2018 Jun; 39(5):924-940. PubMed ID: 29541814
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Semiconductor Sequencing Analysis of Chromosomal Copy Number Variations in Spontaneous Miscarriage.
    Wang MZ; Lin FQ; Li M; He D; Yu QH; Yang XX; Wu YS
    Med Sci Monit; 2017 Nov; 23():5550-5557. PubMed ID: 29162795
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Reference-unbiased copy number variant analysis using CGH microarrays.
    Ju YS; Hong D; Kim S; Park SS; Kim S; Lee S; Park H; Kim JI; Seo JS
    Nucleic Acids Res; 2010 Nov; 38(20):e190. PubMed ID: 20802225
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Diagnosis of fetal submicroscopic chromosomal abnormalities in failed array CGH samples: copy number by sequencing as an alternative to microarrays for invasive fetal testing.
    Cohen K; Tzika A; Wood H; Berri S; Roberts P; Mason G; Sheridan E
    Ultrasound Obstet Gynecol; 2015 Apr; 45(4):394-401. PubMed ID: 25510919
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Array CGH analysis of a cohort of Russian patients with intellectual disability.
    Kashevarova AA; Nazarenko LP; Skryabin NA; Salyukova OA; Chechetkina NN; Tolmacheva EN; Sazhenova EA; Magini P; Graziano C; Romeo G; Kučinskas V; Lebedev IN
    Gene; 2014 Feb; 536(1):145-50. PubMed ID: 24291026
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Mass spectrometry data processing using zero-crossing lines in multi-scale of Gaussian derivative wavelet.
    Nguyen N; Huang H; Oraintara S; Vo A
    Bioinformatics; 2010 Sep; 26(18):i659-65. PubMed ID: 20823336
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.