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Results: 1 to 20 of 42

References for PMC Articles for PubMed (Select 15514107)

1.

Insights from genomic microarrays into structural chromosome rearrangements.

Knijnenburg J, Szuhai K, Giltay J, Molenaar L, Sloos W, Poot M, Tanke HJ, Rosenberg C.

Am J Med Genet A. 2005 Jan 1;132A(1):36-40.

PMID:
15558722
2.

Detecting single DNA copy number variations in complex genomes using one nanogram of starting DNA and BAC-array CGH.

Guillaud-Bataille M, Valent A, Soularue P, Perot C, Inda MM, Receveur A, Smaïli S, Roest Crollius H, Bénard J, Bernheim A, Gidrol X, Danglot G.

Nucleic Acids Res. 2004 Jul 29;32(13):e112.

3.

High-resolution global profiling of genomic alterations with long oligonucleotide microarray.

Brennan C, Zhang Y, Leo C, Feng B, Cauwels C, Aguirre AJ, Kim M, Protopopov A, Chin L.

Cancer Res. 2004 Jul 15;64(14):4744-8.

4.

Use of whole genome amplification and comparative genomic hybridisation to detect chromosomal copy number alterations in cell line material and tumour tissue.

Hughes S, Lim G, Beheshti B, Bayani J, Marrano P, Huang A, Squire JA.

Cytogenet Genome Res. 2004;105(1):18-24.

PMID:
15218253
5.

High resolution microarray comparative genomic hybridisation analysis using spotted oligonucleotides.

Carvalho B, Ouwerkerk E, Meijer GA, Ylstra B.

J Clin Pathol. 2004 Jun;57(6):644-6.

6.

Balanced-PCR amplification allows unbiased identification of genomic copy changes in minute cell and tissue samples.

Wang G, Brennan C, Rook M, Wolfe JL, Leo C, Chin L, Pan H, Liu WH, Price B, Makrigiorgos GM.

Nucleic Acids Res. 2004 May 21;32(9):e76.

7.

Genome coverage and sequence fidelity of phi29 polymerase-based multiple strand displacement whole genome amplification.

Paez JG, Lin M, Beroukhim R, Lee JC, Zhao X, Richter DJ, Gabriel S, Herman P, Sasaki H, Altshuler D, Li C, Meyerson M, Sellers WR.

Nucleic Acids Res. 2004 May 18;32(9):e71.

8.

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.

9.

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 1;64(9):3060-71.

10.

Parallel genotyping of over 10,000 SNPs using a one-primer assay on a high-density oligonucleotide array.

Matsuzaki H, Loi H, Dong S, Tsai YY, Fang J, Law J, Di X, Liu WM, Yang G, Liu G, Huang J, Kennedy GC, Ryder TB, Marcus GA, Walsh PS, Shriver MD, Puck JM, Jones KW, Mei R.

Genome Res. 2004 Mar;14(3):414-25. Erratum in: Genome Res. 2004 Apr;14(4):786.

11.

A tiling resolution DNA microarray with complete coverage of the human genome.

Ishkanian AS, Malloff CA, Watson SK, DeLeeuw RJ, Chi B, Coe BP, Snijders A, Albertson DG, Pinkel D, Marra MA, Ling V, MacAulay C, Lam WL.

Nat Genet. 2004 Mar;36(3):299-303. Epub 2004 Feb 15.

PMID:
14981516
12.

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.

13.

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. Epub 2003 Sep 15.

14.

Unbiased whole-genome amplification directly from clinical samples.

Hosono S, Faruqi AF, Dean FB, Du Y, Sun Z, Wu X, Du J, Kingsmore SF, Egholm M, Lasken RS.

Genome Res. 2003 May;13(5):954-64. Epub 2003 Apr 14.

15.

DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones.

Fiegler H, Carr P, Douglas EJ, Burford DC, Hunt S, Scott CE, Smith J, Vetrie D, Gorman P, Tomlinson IP, Carter NP.

Genes Chromosomes Cancer. 2003 Apr;36(4):361-74. Erratum in: Genes Chromosomes Cancer. 2003 Jun;37(2):223.

PMID:
12619160
16.
17.

Whole genome analysis of genetic alterations in small DNA samples using hyperbranched strand displacement amplification and array-CGH.

Lage JM, Leamon JH, Pejovic T, Hamann S, Lacey M, Dillon D, Segraves R, Vossbrinck B, González A, Pinkel D, Albertson DG, Costa J, Lizardi PM.

Genome Res. 2003 Feb;13(2):294-307.

18.

Comprehensive human genome amplification using multiple displacement amplification.

Dean FB, Hosono S, Fang L, Wu X, Faruqi AF, Bray-Ward P, Sun Z, Zong Q, Du Y, Du J, Driscoll M, Song W, Kingsmore SF, Egholm M, Lasken RS.

Proc Natl Acad Sci U S A. 2002 Apr 16;99(8):5261-6.

19.

Assembly of microarrays for genome-wide measurement of DNA copy number.

Snijders AM, Nowak N, Segraves R, Blackwood S, Brown N, Conroy J, Hamilton G, Hindle AK, Huey B, Kimura K, Law S, Myambo K, Palmer J, Ylstra B, Yue JP, Gray JW, Jain AN, Pinkel D, Albertson DG.

Nat Genet. 2001 Nov;29(3):263-4.

PMID:
11687795
20.
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