BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

121 related articles for article (PubMed ID: 17272296)

  • 1. 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]  

  • 2. 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]  

  • 3. Human and mouse oligonucleotide-based array CGH.
    van den Ijssel P; Tijssen M; Chin SF; Eijk P; Carvalho B; Hopmans E; Holstege H; Bangarusamy DK; Jonkers J; Meijer GA; Caldas C; Ylstra B
    Nucleic Acids Res; 2005 Dec; 33(22):e192. PubMed ID: 16361265
    [TBL] [Abstract][Full Text] [Related]  

  • 4. BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH).
    Ylstra B; van den Ijssel P; Carvalho B; Brakenhoff RH; Meijer GA
    Nucleic Acids Res; 2006; 34(2):445-50. PubMed ID: 16439806
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. CGHPRO -- a comprehensive data analysis tool for array CGH.
    Chen W; Erdogan F; Ropers HH; Lenzner S; Ullmann R
    BMC Bioinformatics; 2005 Apr; 6():85. PubMed ID: 15807904
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A forward-backward fragment assembling algorithm for the identification of genomic amplification and deletion breakpoints using high-density single nucleotide polymorphism (SNP) array.
    Yu T; Ye H; Sun W; Li KC; Chen Z; Jacobs S; Bailey DK; Wong DT; Zhou X
    BMC Bioinformatics; 2007 May; 8():145. PubMed ID: 17477871
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas.
    Espinosa AB; Mackintosh C; Maíllo A; Gutierrez L; Sousa P; Merino M; Ortiz J; de Alava E; Orfao A; Tabernero MD
    Eur J Hum Genet; 2008 Dec; 16(12):1450-8. PubMed ID: 18628790
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Determination of amplicon boundaries at 20q13.2 in tissue samples of human gastric adenocarcinomas by high-resolution microarray comparative genomic hybridization.
    Weiss MM; Snijders AM; Kuipers EJ; Ylstra B; Pinkel D; Meuwissen SG; van Diest PJ; Albertson DG; Meijer GA
    J Pathol; 2003 Jul; 200(3):320-6. PubMed ID: 12845628
    [TBL] [Abstract][Full Text] [Related]  

  • 11. SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data.
    Price TS; Regan R; Mott R; Hedman A; Honey B; Daniels RJ; Smith L; Greenfield A; Tiganescu A; Buckle V; Ventress N; Ayyub H; Salhan A; Pedraza-Diaz S; Broxholme J; Ragoussis J; Higgs DR; Flint J; Knight SJ
    Nucleic Acids Res; 2005; 33(11):3455-64. PubMed ID: 15961730
    [TBL] [Abstract][Full Text] [Related]  

  • 12. High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.
    Urban AE; Korbel JO; Selzer R; Richmond T; Hacker A; Popescu GV; Cubells JF; Green R; Emanuel BS; Gerstein MB; Weissman SM; Snyder M
    Proc Natl Acad Sci U S A; 2006 Mar; 103(12):4534-9. PubMed ID: 16537408
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data.
    Lai WR; Johnson MD; Kucherlapati R; Park PJ
    Bioinformatics; 2005 Oct; 21(19):3763-70. PubMed ID: 16081473
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome-wide detection of chromosomal imbalances in tumors using BAC microarrays.
    Cai WW; Mao JH; Chow CW; Damani S; Balmain A; Bradley A
    Nat Biotechnol; 2002 Apr; 20(4):393-6. PubMed ID: 11923847
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detecting single DNA copy number variations in complex genomes using one nanogram of starting DNA and BAC-array CGH.
    Guillaud-Bataille M; Valent A; Soularue P; Perot C; Inda MM; Receveur A; Smaïli S; Roest Crollius H; Bénard J; Bernheim A; Gidrol X; Danglot G
    Nucleic Acids Res; 2004 Jul; 32(13):e112. PubMed ID: 15284333
    [TBL] [Abstract][Full Text] [Related]  

  • 16. TAFFYS: An Integrated Tool for Comprehensive Analysis of Genomic Aberrations in Tumor Samples.
    Liu Y; Li A; Feng H; Wang M
    PLoS One; 2015; 10(6):e0129835. PubMed ID: 26111017
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A statistical method to detect chromosomal regions with DNA copy number alterations using SNP-array-based CGH data.
    Lai Y; Zhao H
    Comput Biol Chem; 2005 Feb; 29(1):47-54. PubMed ID: 15680585
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Chromosomal copy number changes in patients with non-syndromic X linked mental retardation detected by array CGH.
    Lugtenberg D; de Brouwer AP; Kleefstra T; Oudakker AR; Frints SG; Schrander-Stumpel CT; Fryns JP; Jensen LR; Chelly J; Moraine C; Turner G; Veltman JA; Hamel BC; de Vries BB; van Bokhoven H; Yntema HG
    J Med Genet; 2006 Apr; 43(4):362-70. PubMed ID: 16169931
    [TBL] [Abstract][Full Text] [Related]  

  • 20. High resolution oligonucleotide CGH using DNA from archived prostate tissue.
    Paris PL; Sridharan S; Scheffer A; Tsalenko A; Bruhn L; Collins C
    Prostate; 2007 Sep; 67(13):1447-55. PubMed ID: 17654530
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.