BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

555 related articles for article (PubMed ID: 16899659)

  • 1. High-resolution genomic profiling of chromosomal aberrations using Infinium whole-genome genotyping.
    Peiffer DA; Le JM; Steemers FJ; Chang W; Jenniges T; Garcia F; Haden K; Li J; Shaw CA; Belmont J; Cheung SW; Shen RM; Barker DL; Gunderson KL
    Genome Res; 2006 Sep; 16(9):1136-48. PubMed ID: 16899659
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ploidy status and copy number aberrations in primary glioblastomas defined by integrated analysis of allelic ratios, signal ratios and loss of heterozygosity using 500K SNP Mapping Arrays.
    Gardina PJ; Lo KC; Lee W; Cowell JK; Turpaz Y
    BMC Genomics; 2008 Oct; 9():489. PubMed ID: 18928532
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios.
    Staaf J; Vallon-Christersson J; Lindgren D; Juliusson G; Rosenquist R; Höglund M; Borg A; Ringnér M
    BMC Bioinformatics; 2008 Oct; 9():409. PubMed ID: 18831757
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole-genome profiling of chromosomal aberrations in hepatoblastoma using high-density single-nucleotide polymorphism genotyping microarrays.
    Suzuki M; Kato M; Yuyan C; Takita J; Sanada M; Nannya Y; Yamamoto G; Takahashi A; Ikeda H; Kuwano H; Ogawa S; Hayashi Y
    Cancer Sci; 2008 Mar; 99(3):564-70. PubMed ID: 18271875
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Whole genome DNA copy number changes identified by high density oligonucleotide arrays.
    Huang J; Wei W; Zhang J; Liu G; Bignell GR; Stratton MR; Futreal PA; Wooster R; Jones KW; Shapero MH
    Hum Genomics; 2004 May; 1(4):287-99. PubMed ID: 15588488
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical significance of previously cryptic copy number alterations and loss of heterozygosity in pediatric acute myeloid leukemia and myelodysplastic syndrome determined using combined array comparative genomic hybridization plus single-nucleotide polymorphism microarray analyses.
    Koh KN; Lee JO; Seo EJ; Lee SW; Suh JK; Im HJ; Seo JJ
    J Korean Med Sci; 2014 Jul; 29(7):926-33. PubMed ID: 25045224
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan.
    Ting JC; Ye Y; Thomas GH; Ruczinski I; Pevsner J
    BMC Bioinformatics; 2006 Jan; 7():25. PubMed ID: 16420694
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Allelic imbalance analysis by high-density single-nucleotide polymorphic allele (SNP) array with whole genome amplified DNA.
    Wong KK; Tsang YT; Shen J; Cheng RS; Chang YM; Man TK; Lau CC
    Nucleic Acids Res; 2004 May; 32(9):e69. PubMed ID: 15148342
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A genome-wide study of cytogenetic changes in colorectal cancer using SNP microarrays: opportunities for future personalized treatment.
    Jasmine F; Rahaman R; Dodsworth C; Roy S; Paul R; Raza M; Paul-Brutus R; Kamal M; Ahsan H; Kibriya MG
    PLoS One; 2012; 7(2):e31968. PubMed ID: 22363777
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cancer Sample Analysis Utilizing Single-Nucleotide Polymorphism Array and Array Comparative Genomic Hybridization.
    Kang B; Xiao H; Ackley T; Shao L
    Methods Mol Biol; 2024; 2825():151-171. PubMed ID: 38913308
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Progress in concurrent analysis of loss of heterozygosity and comparative genomic hybridization utilizing high density single nucleotide polymorphism arrays.
    Zhou X; Rao NP; Cole SW; Mok SC; Chen Z; Wong DT
    Cancer Genet Cytogenet; 2005 May; 159(1):53-7. PubMed ID: 15860358
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex changes and multiple forms of chromosomal instability in colorectal cancers.
    Gaasenbeek M; Howarth K; Rowan AJ; Gorman PA; Jones A; Chaplin T; Liu Y; Bicknell D; Davison EJ; Fiegler H; Carter NP; Roylance RR; Tomlinson IP
    Cancer Res; 2006 Apr; 66(7):3471-9. PubMed ID: 16585170
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Loss of heterozygosity and copy number abnormality in clear cell renal cell carcinoma discovered by high-density affymetrix 10K single nucleotide polymorphism mapping array.
    Toma MI; Grosser M; Herr A; Aust DE; Meye A; Hoefling C; Fuessel S; Wuttig D; Wirth MP; Baretton GB
    Neoplasia; 2008 Jul; 10(7):634-42. PubMed ID: 18592004
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Detection of chromosome changes by CGH, array-CGH and SNP array techniques in tumours].
    Vosecká T; Musil Z; Vícha A
    Cesk Patol; 2014 Jan; 50(1):25-9. PubMed ID: 24624983
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genome-wide analysis of recurrent copy-number alterations and copy-neutral loss of heterozygosity in head and neck squamous cell carcinoma.
    Marescalco MS; Capizzi C; Condorelli DF; Barresi V
    J Oral Pathol Med; 2014 Jan; 43(1):20-7. PubMed ID: 23750501
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genome-wide genetic characterization of bladder cancer: a comparison of high-density single-nucleotide polymorphism arrays and PCR-based microsatellite analysis.
    Hoque MO; Lee CC; Cairns P; Schoenberg M; Sidransky D
    Cancer Res; 2003 May; 63(9):2216-22. PubMed ID: 12727842
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide allelic state analysis on flow-sorted tumor fractions provides an accurate measure of chromosomal aberrations.
    Corver WE; Middeldorp A; ter Haar NT; Jordanova ES; van Puijenbroek M; van Eijk R; Cornelisse CJ; Fleuren GJ; Morreau H; Oosting J; van Wezel T
    Cancer Res; 2008 Dec; 68(24):10333-40. PubMed ID: 19074902
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arrays.
    Pfeifer D; Pantic M; Skatulla I; Rawluk J; Kreutz C; Martens UM; Fisch P; Timmer J; Veelken H
    Blood; 2007 Feb; 109(3):1202-10. PubMed ID: 17053054
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array.
    Hu N; Wang C; Hu Y; Yang HH; Kong LH; Lu N; Su H; Wang QH; Goldstein AM; Buetow KH; Emmert-Buck MR; Taylor PR; Lee MP
    BMC Genomics; 2006 Nov; 7():299. PubMed ID: 17134496
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 28.