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 *

160 related articles for article (PubMed ID: 15534219)

  • 1. A versatile statistical analysis algorithm to detect genome copy number variation.
    Daruwala RS; Rudra A; Ostrer H; Lucito R; Wigler M; Mishra B
    Proc Natl Acad Sci U S A; 2004 Nov; 101(46):16292-7. PubMed ID: 15534219
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation.
    Lucito R; Healy J; Alexander J; Reiner A; Esposito D; Chi M; Rodgers L; Brady A; Sebat J; Troge J; West JA; Rostan S; Nguyen KC; Powers S; Ye KQ; Olshen A; Venkatraman E; Norton L; Wigler M
    Genome Res; 2003 Oct; 13(10):2291-305. PubMed ID: 12975311
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Assessing the significance of conserved genomic aberrations using high resolution genomic microarrays.
    Guttman M; Mies C; Dudycz-Sulicz K; Diskin SJ; Baldwin DA; Stoeckert CJ; Grant GR
    PLoS Genet; 2007 Aug; 3(8):e143. PubMed ID: 17722985
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Challenges in array comparative genomic hybridization for the analysis of cancer samples.
    Nowak NJ; Miecznikowski J; Moore SR; Gaile D; Bobadilla D; Smith DD; Kernstine K; Forman SJ; Mhawech-Fauceglia P; Reid M; Stoler D; Loree T; Rigual N; Sullivan M; Weiss LM; Hicks D; Slovak ML
    Genet Med; 2007 Sep; 9(9):585-95. PubMed ID: 17873646
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Denoising array-based comparative genomic hybridization data using wavelets.
    Hsu L; Self SG; Grove D; Randolph T; Wang K; Delrow JJ; Loo L; Porter P
    Biostatistics; 2005 Apr; 6(2):211-26. PubMed ID: 15772101
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Construction and application of a full-coverage, high-resolution, human chromosome 8q genomic microarray for comparative genomic hybridization.
    van Duin M; van Marion R; Watson JE; Paris PL; Lapuk A; Brown N; Oseroff VV; Albertson DG; Pinkel D; de Jong P; Nacheva EP; Dinjens W; van Dekken H; Collins C
    Cytometry A; 2005; 63(1):10-9. PubMed ID: 15619731
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical array-based karyotyping of breast cancer with equivocal HER2 status resolves gene copy number and reveals chromosome 17 complexity.
    Gunn S; Yeh IT; Lytvak I; Tirtorahardjo B; Dzidic N; Zadeh S; Kim J; McCaskill C; Lim L; Gorre M; Mohammed M
    BMC Cancer; 2010 Jul; 10():396. PubMed ID: 20667129
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Visualization-based discovery and analysis of genomic aberrations in microarray data.
    Myers CL; Chen X; Troyanskaya OG
    BMC Bioinformatics; 2005 Jun; 6():146. PubMed ID: 15953389
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.
    Pinkel D; Segraves R; Sudar D; Clark S; Poole I; Kowbel D; Collins C; Kuo WL; Chen C; Zhai Y; Dairkee SH; Ljung BM; Gray JW; Albertson DG
    Nat Genet; 1998 Oct; 20(2):207-11. PubMed ID: 9771718
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. High resolution genomic analysis of sporadic breast cancer using array-based comparative genomic hybridization.
    Naylor TL; Greshock J; Wang Y; Colligon T; Yu QC; Clemmer V; Zaks TZ; Weber BL
    Breast Cancer Res; 2005; 7(6):R1186-98. PubMed ID: 16457699
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comparison of the Agilent, ROMA/NimbleGen and Illumina platforms for classification of copy number alterations in human breast tumors.
    Baumbusch LO; Aarøe J; Johansen FE; Hicks J; Sun H; Bruhn L; Gunderson K; Naume B; Kristensen VN; Liestøl K; Børresen-Dale AL; Lingjaerde OC
    BMC Genomics; 2008 Aug; 9():379. PubMed ID: 18691401
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of significant regional genetic variations using continuous CNV values in aCGH data.
    Kim KY; Lee GY; Kim J; Jeung HC; Chung HC; Rha SY
    Genomics; 2009 Nov; 94(5):317-23. PubMed ID: 19699295
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Comparative genomic hybridization.
    Pinkel D; Albertson DG
    Annu Rev Genomics Hum Genet; 2005; 6():331-54. PubMed ID: 16124865
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Global search for chromosomal abnormalities in infiltrating ductal carcinoma of the breast using array-comparative genomic hybridization.
    Somiari SB; Shriver CD; He J; Parikh K; Jordan R; Hooke J; Hu H; Deyarmin B; Lubert S; Malicki L; Heckman C; Somiari RI
    Cancer Genet Cytogenet; 2004 Dec; 155(2):108-18. PubMed ID: 15571796
    [TBL] [Abstract][Full Text] [Related]  

  • 18. High frequency of common DNA copy number abnormalities detected by bacterial artificial chromosome array comparative genomic hybridization in 24 breast cancer cell lines.
    Saito S; Morita K; Hirano T
    Hum Cell; 2009 Feb; 22(1):1-10. PubMed ID: 19222606
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Breast tumor copy number aberration phenotypes and genomic instability.
    Fridlyand J; Snijders AM; Ylstra B; Li H; Olshen A; Segraves R; Dairkee S; Tokuyasu T; Ljung BM; Jain AN; McLennan J; Ziegler J; Chin K; Devries S; Feiler H; Gray JW; Waldman F; Pinkel D; Albertson DG
    BMC Cancer; 2006 Apr; 6():96. PubMed ID: 16620391
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.
    Kloth JN; Oosting J; van Wezel T; Szuhai K; Knijnenburg J; Gorter A; Kenter GG; Fleuren GJ; Jordanova ES
    BMC Genomics; 2007 Feb; 8():53. PubMed ID: 17311676
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.