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    Results: 1 to 20 of 411

    1.

    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 18;7:25.PMID: 16420694 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio.

    Ting JC, Roberson ED, Miller ND, Lysholm-Bernacchi A, Stephan DA, Capone GT, Ruczinski I, Thomas GH, Pevsner J.

    Hum Mutat. 2007 Dec;28(12):1225-35.PMID: 17661425 [PubMed - indexed for MEDLINE]Related articles

    3.

    SNPchip: R classes and methods for SNP array data.

    Scharpf RB, Ting JC, Pevsner J, Ruczinski I.

    Bioinformatics. 2007 Mar 1;23(5):627-8. Epub 2007 Jan 4.PMID: 17204461 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    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.PMID: 18592004 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    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. Epub 2006 Aug 9.PMID: 16899659 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Visualization of genomic aberrations using Affymetrix SNP arrays.

    Müller A, Holzmann K, Kestler HA.

    Bioinformatics. 2007 Feb 15;23(4):496-7. Epub 2006 Nov 30.PMID: 17138589 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays.

    Carr J, Bown NP, Case MC, Hall AG, Lunec J, Tweddle DA.

    Cancer Genet Cytogenet. 2007 Jan 15;172(2):127-38.PMID: 17213021 [PubMed - indexed for MEDLINE]Related articles

    8.

    High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs.

    Slater HR, Bailey DK, Ren H, Cao M, Bell K, Nasioulas S, Henke R, Choo KH, Kennedy GC.

    Am J Hum Genet. 2005 Nov;77(5):709-26. Epub 2005 Sep 16. Erratum in: Am J Hum Genet. 2006 Mar;78(3):526. PMID: 16252233 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Frequent occurrence of uniparental disomy in colorectal cancer.

    Andersen CL, Wiuf C, Kruhøffer M, Korsgaard M, Laurberg S, Ørntoft TF.

    Carcinogenesis. 2007 Jan;28(1):38-48. Epub 2006 Jun 13.PMID: 16774939 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Direct inference of SNP heterozygosity rates and resolution of LOH detection.

    Li X, Self SG, Galipeau PC, Paulson TG, Reid BJ.

    PLoS Comput Biol. 2007 Nov;3(11):e244.PMID: 18052545 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    SNP-PHAGE--High throughput SNP discovery pipeline.

    Matukumalli LK, Grefenstette JJ, Hyten DL, Choi IY, Cregan PB, Van Tassell CP.

    BMC Bioinformatics. 2006 Oct 23;7:468.PMID: 17059604 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Genomewide scan for loss of heterozygosity and chromosomal amplification in breast carcinoma using single-nucleotide polymorphism arrays.

    Argos M, Kibriya MG, Jasmine F, Olopade OI, Su T, Hibshoosh H, Ahsan H.

    Cancer Genet Cytogenet. 2008 Apr 15;182(2):69-74.PMID: 18406867 [PubMed - indexed for MEDLINE]Related articles

    13.

    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 21;9:204.PMID: 18426588 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?

    Bejjani BA, Saleki R, Ballif BC, Rorem EA, Sundin K, Theisen A, Kashork CD, Shaffer LG.

    Am J Med Genet A. 2005 Apr 30;134(3):259-67.PMID: 15723295 [PubMed - indexed for MEDLINE]Related articles

    15.

    AffyMAPSDetector: a software tool to characterize Affymetrix GeneChip expression arrays with respect to SNPs.

    Kumari S, Verma LK, Weller JW.

    BMC Bioinformatics. 2007 Jul 30;8:276.PMID: 17663786 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Molecular allelokaryotyping of early-stage, untreated chronic lymphocytic leukemia.

    Lehmann S, Ogawa S, Raynaud SD, Sanada M, Nannya Y, Ticchioni M, Bastard C, Kawamata N, Koeffler HP.

    Cancer. 2008 Mar 15;112(6):1296-305.PMID: 18246537 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    SNP-VISTA: an interactive SNP visualization tool.

    Shah N, Teplitsky MV, Minovitsky S, Pennacchio LA, Hugenholtz P, Hamann B, Dubchak IL.

    BMC Bioinformatics. 2005 Dec 8;6:292.PMID: 16336665 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    High-resolution array copy number analyses for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors: four cases of homozygous deletions of the CDKN2A gene.

    Carén H, Erichsen J, Olsson L, Enerbäck C, Sjöberg RM, Abrahamsson J, Kogner P, Martinsson T.

    BMC Genomics. 2008 Jul 29;9:353.PMID: 18664255 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    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 17;32(9):e69.PMID: 15148342 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays.

    Wang L, Fidler C, Nadig N, Giagounidis A, Della Porta MG, Malcovati L, Killick S, Gattermann N, Aul C, Boultwood J, Wainscoat JS.

    Haematologica. 2008 Jul;93(7):994-1000. Epub 2008 May 27.PMID: 18508791 [PubMed - indexed for MEDLINE]Related articlesFree article

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