BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

325 related articles for article (PubMed ID: 16322765)

  • 1. 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]  

  • 2. PLASQ: a generalized linear model-based procedure to determine allelic dosage in cancer cells from SNP array data.
    Laframboise T; Harrington D; Weir BA
    Biostatistics; 2007 Apr; 8(2):323-36. PubMed ID: 16787995
    [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. High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray.
    Yin D; Ogawa S; Kawamata N; Tunici P; Finocchiaro G; Eoli M; Ruckert C; Huynh T; Liu G; Kato M; Sanada M; Jauch A; Dugas M; Black KL; Koeffler HP
    Mol Cancer Res; 2009 May; 7(5):665-77. PubMed ID: 19435819
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Improvements in the analysis strategy make single nucleotide polymorphism analysis a powerful tool in the detection and characterization of amplified chromosomal regions in human tumors.
    Korsching E; Agelopolous K; Schmidt H; Buchroth I; Gosheger G; Wülfing P; Boecker W; Brandt B; Buerger H
    Pathobiology; 2006; 73(1):18-25. PubMed ID: 16785764
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Toward accurate high-throughput SNP genotyping in the presence of inherited copy number variation.
    Macconaill LE; Aldred MA; Lu X; Laframboise T
    BMC Genomics; 2007 Jul; 8():211. PubMed ID: 17608949
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Major copy proportion analysis of tumor samples using SNP arrays.
    Li C; Beroukhim R; Weir BA; Winckler W; Garraway LA; Sellers WR; Meyerson M
    BMC Bioinformatics; 2008 Apr; 9():204. PubMed ID: 18426588
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genome-wide allelic imbalance analysis of pediatric gliomas by single nucleotide polymorphic allele array.
    Wong KK; Tsang YT; Chang YM; Su J; Di Francesco AM; Meco D; Riccardi R; Perlaky L; Dauser RC; Adesina A; Bhattacharjee M; Chintagumpala M; Lau CC
    Cancer Res; 2006 Dec; 66(23):11172-8. PubMed ID: 17145861
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Systematic assessment of copy number variant detection via genome-wide SNP genotyping.
    Cooper GM; Zerr T; Kidd JM; Eichler EE; Nickerson DA
    Nat Genet; 2008 Oct; 40(10):1199-203. PubMed ID: 18776910
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The consequences of uniparental disomy and copy number neutral loss-of-heterozygosity during human development and cancer.
    Lapunzina P; Monk D
    Biol Cell; 2011 Jul; 103(7):303-17. PubMed ID: 21651501
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Polymorphisms, mutations, and amplification of the EGFR gene in non-small cell lung cancers.
    Nomura M; Shigematsu H; Li L; Suzuki M; Takahashi T; Estess P; Siegelman M; Feng Z; Kato H; Marchetti A; Shay JW; Spitz MR; Wistuba II; Minna JD; Gazdar AF
    PLoS Med; 2007 Apr; 4(4):e125. PubMed ID: 17455987
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays.
    Zhao X; Li C; Paez JG; Chin K; Jänne PA; Chen TH; Girard L; Minna J; Christiani D; Leo C; Gray JW; Sellers WR; Meyerson M
    Cancer Res; 2004 May; 64(9):3060-71. PubMed ID: 15126342
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. High-resolution analysis of DNA copy number using oligonucleotide microarrays.
    Bignell GR; Huang J; Greshock J; Watt S; Butler A; West S; Grigorova M; Jones KW; Wei W; Stratton MR; Futreal PA; Weber B; Shapero MH; Wooster R
    Genome Res; 2004 Feb; 14(2):287-95. PubMed ID: 14762065
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inferring loss-of-heterozygosity from unpaired tumors using high-density oligonucleotide SNP arrays.
    Beroukhim R; Lin M; Park Y; Hao K; Zhao X; Garraway LA; Fox EA; Hochberg EP; Mellinghoff IK; Hofer MD; Descazeaud A; Rubin MA; Meyerson M; Wong WH; Sellers WR; Li C
    PLoS Comput Biol; 2006 May; 2(5):e41. PubMed ID: 16699594
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Integrated detection and population-genetic analysis of SNPs and copy number variation.
    McCarroll SA; Kuruvilla FG; Korn JM; Cawley S; Nemesh J; Wysoker A; Shapero MH; de Bakker PI; Maller JB; Kirby A; Elliott AL; Parkin M; Hubbell E; Webster T; Mei R; Veitch J; Collins PJ; Handsaker R; Lincoln S; Nizzari M; Blume J; Jones KW; Rava R; Daly MJ; Gabriel SB; Altshuler D
    Nat Genet; 2008 Oct; 40(10):1166-74. PubMed ID: 18776908
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High-resolution single nucleotide polymorphism array analysis of epithelial ovarian cancer reveals numerous microdeletions and amplifications.
    Gorringe KL; Jacobs S; Thompson ER; Sridhar A; Qiu W; Choong DY; Campbell IG
    Clin Cancer Res; 2007 Aug; 13(16):4731-9. PubMed ID: 17699850
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.
    Huang J; Wei W; Chen J; Zhang J; Liu G; Di X; Mei R; Ishikawa S; Aburatani H; Jones KW; Shapero MH
    BMC Bioinformatics; 2006 Feb; 7():83. PubMed ID: 16504045
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.