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 *

122 related articles for article (PubMed ID: 17048389)

  • 21. MutaGeneSys: estimating individual disease susceptibility based on genome-wide SNP array data.
    Stoyanovich J; Pe'er I
    Bioinformatics; 2008 Feb; 24(3):440-2. PubMed ID: 18048395
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Elucidating the altered transcriptional programs in breast cancer using independent component analysis.
    Teschendorff AE; Journée M; Absil PA; Sepulchre R; Caldas C
    PLoS Comput Biol; 2007 Aug; 3(8):e161. PubMed ID: 17708679
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Evaluation of gene importance in microarray data based upon probability of selection.
    Fu LM; Fu-Liu CS
    BMC Bioinformatics; 2005 Mar; 6():67. PubMed ID: 15784140
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Markers improve clustering of CGH data.
    Liu J; Ranka S; Kahveci T
    Bioinformatics; 2007 Feb; 23(4):450-7. PubMed ID: 17150994
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Meta-analysis of gene expression data: a predictor-based approach.
    Fishel I; Kaufman A; Ruppin E
    Bioinformatics; 2007 Jul; 23(13):1599-606. PubMed ID: 17463023
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Outcome signature genes in breast cancer: is there a unique set?
    Ein-Dor L; Kela I; Getz G; Givol D; Domany E
    Bioinformatics; 2005 Jan; 21(2):171-8. PubMed ID: 15308542
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A segmental maximum a posteriori approach to genome-wide copy number profiling.
    Andersson R; Bruder CE; Piotrowski A; Menzel U; Nord H; Sandgren J; Hvidsten TR; Diaz de Ståhl T; Dumanski JP; Komorowski J
    Bioinformatics; 2008 Mar; 24(6):751-8. PubMed ID: 18204059
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Gene expression profiling and gene copy-number changes in malignant mesothelioma cell lines.
    Zanazzi C; Hersmus R; Veltman IM; Gillis AJ; van Drunen E; Beverloo HB; Hegmans JP; Verweij M; Lambrecht BN; Oosterhuis JW; Looijenga LH
    Genes Chromosomes Cancer; 2007 Oct; 46(10):895-908. PubMed ID: 17620293
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The latent process decomposition of cDNA microarray data sets.
    Rogers S; Girolami M; Campbell C; Breitling R
    IEEE/ACM Trans Comput Biol Bioinform; 2005; 2(2):143-56. PubMed ID: 17044179
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Detecting gene copy number fluctuations in tumor cells by microarray analysis of genomic representations.
    Lucito R; West J; Reiner A; Alexander J; Esposito D; Mishra B; Powers S; Norton L; Wigler M
    Genome Res; 2000 Nov; 10(11):1726-36. PubMed ID: 11076858
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Gene selection using a two-level hierarchical Bayesian model.
    Bae K; Mallick BK
    Bioinformatics; 2004 Dec; 20(18):3423-30. PubMed ID: 15256404
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Aging impacts transcriptomes but not genomes of hormone-dependent breast cancers.
    Yau C; Fedele V; Roydasgupta R; Fridlyand J; Hubbard A; Gray JW; Chew K; Dairkee SH; Moore DH; Schittulli F; Tommasi S; Paradiso A; Albertson DG; Benz CC
    Breast Cancer Res; 2007; 9(5):R59. PubMed ID: 17850661
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Gene expression databases and data mining.
    Anderle P; Duval M; Draghici S; Kuklin A; Littlejohn TG; Medrano JF; Vilanova D; Roberts MA
    Biotechniques; 2003 Mar; Suppl():36-44. PubMed ID: 12664683
    [TBL] [Abstract][Full Text] [Related]  

  • 34. High-resolution copy number and gene expression microarray analyses of head and neck squamous cell carcinoma cell lines of tongue and larynx.
    Järvinen AK; Autio R; Kilpinen S; Saarela M; Leivo I; Grénman R; Mäkitie AA; Monni O
    Genes Chromosomes Cancer; 2008 Jun; 47(6):500-9. PubMed ID: 18314910
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Array comparative genomic hybridization copy number profiling: a new tool for translational research in solid malignancies.
    Costa JL; Meijer G; Ylstra B; Caldas C
    Semin Radiat Oncol; 2008 Apr; 18(2):98-104. PubMed ID: 18314064
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular decomposition of complex clinical phenotypes using biologically structured analysis of microarray data.
    Lottaz C; Spang R
    Bioinformatics; 2005 May; 21(9):1971-8. PubMed ID: 15677704
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Allele-specific amplification in cancer revealed by SNP array analysis.
    LaFramboise T; Weir BA; Zhao X; Beroukhim R; Li C; Harrington D; Sellers WR; Meyerson M
    PLoS Comput Biol; 2005 Nov; 1(6):e65. PubMed ID: 16322765
    [TBL] [Abstract][Full Text] [Related]  

  • 38. CNAnova: a new approach for finding recurrent copy number abnormalities in cancer SNP microarray data.
    Ivakhno S; Tavaré S
    Bioinformatics; 2010 Jun; 26(11):1395-402. PubMed ID: 20403815
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genome-driven integrated classification of breast cancer validated in over 7,500 samples.
    Ali HR; Rueda OM; Chin SF; Curtis C; Dunning MJ; Aparicio SA; Caldas C
    Genome Biol; 2014 Aug; 15(8):431. PubMed ID: 25164602
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Avoiding model selection bias in small-sample genomic datasets.
    Berrar D; Bradbury I; Dubitzky W
    Bioinformatics; 2006 May; 22(10):1245-50. PubMed ID: 16500931
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.