Pesquisa | Biblioteca Virtual em Saúde

1.

Genome-wide, high-resolution detection of copy number, loss of heterozygosity, and genotypes from formalin-fixed, paraffin-embedded tumor tissue using microarrays.

Jacobs, Sharoni; Thompson, Ella R; Nannya, Yasuhito; Yamamoto, Go; Pillai, Raji; Ogawa, Seishi; Bailey, Dione K; Campbell, Ian G.

Cancer Res; 67(6): 2544-51, 2007 Mar 15.

Artigo em Inglês | MEDLINE | ID: mdl-17363572

2.

A forward-backward fragment assembling algorithm for the identification of genomic amplification and deletion breakpoints using high-density single nucleotide polymorphism (SNP) array.

Yu, Tianwei; Ye, Hui; Sun, Wei; Li, Ker-Chau; Chen, Zugen; Jacobs, Sharoni; Bailey, Dione K; Wong, David T; Zhou, Xiaofeng.

BMC Bioinformatics; 8: 145, 2007 May 03.

Artigo em Inglês | MEDLINE | ID: mdl-17477871

3.

A whole genome long-range haplotype (WGLRH) test for detecting imprints of positive selection in human populations.

Zhang, Chun; Bailey, Dione K; Awad, Tarif; Liu, Guoying; Xing, Guoliang; Cao, Manqiu; Valmeekam, Venu; Retief, Jacques; Matsuzaki, Hajime; Taub, Margaret; Seielstad, Mark; Kennedy, Giulia C.

Bioinformatics; 22(17): 2122-8, 2006 Sep 01.

Artigo em Inglês | MEDLINE | ID: mdl-16845142

4.

A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.

Nannya, Yasuhito; Sanada, Masashi; Nakazaki, Kumi; Hosoya, Noriko; Wang, Lili; Hangaishi, Akira; Kurokawa, Mineo; Chiba, Shigeru; Bailey, Dione K; Kennedy, Giulia C; Ogawa, Seishi.

Cancer Res; 65(14): 6071-9, 2005 Jul 15.

Artigo em Inglês | MEDLINE | ID: mdl-16024607

5.

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation.

Friedman, J M; Baross, Agnes; Delaney, Allen D; Ally, Adrian; Arbour, Laura; Armstrong, Linlea; Asano, Jennifer; Bailey, Dione K; Barber, Sarah; Birch, Patricia; Brown-John, Mabel; Cao, Manqiu; Chan, Susanna; Charest, David L; Farnoud, Noushin; Fernandes, Nicole; Flibotte, Stephane; Go, Anne; Gibson, William T; Holt, Robert A; Jones, Steven J M; Kennedy, Giulia C; Krzywinski, Martin; Langlois, Sylvie; Li, Haiyan I; McGillivray, Barbara C; Nayar, Tarun; Pugh, Trevor J; Rajcan-Separovic, Evica; Schein, Jacqueline E; Schnerch, Angelique; Siddiqui, Asim; Van Allen, Margot I; Wilson, Gary; Yong, Siu-Li; Zahir, Farah; Eydoux, Patrice; Marra, Marco A.

Am J Hum Genet; 79(3): 500-13, 2006 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-16909388

6.

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

Slater, Howard R; Bailey, Dione K; Ren, Hua; Cao, Manqiu; Bell, Katrina; Nasioulas, Steven; Henke, Robert; Choo, K H Andy; Kennedy, Giulia C.

Am J Hum Genet; 77(5): 709-26, 2005 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-16252233

7.

Genomic maps and comparative analysis of histone modifications in human and mouse.

Bernstein, Bradley E; Kamal, Michael; Lindblad-Toh, Kerstin; Bekiranov, Stefan; Bailey, Dione K; Huebert, Dana J; McMahon, Scott; Karlsson, Elinor K; Kulbokas, Edward J; Gingeras, Thomas R; Schreiber, Stuart L; Lander, Eric S.

Cell; 120(2): 169-81, 2005 Jan 28.

Artigo em Inglês | MEDLINE | ID: mdl-15680324

8.

Transcriptional maps of 10 human chromosomes at 5-nucleotide resolution.

Cheng, Jill; Kapranov, Philipp; Drenkow, Jorg; Dike, Sujit; Brubaker, Shane; Patel, Sandeep; Long, Jeffrey; Stern, David; Tammana, Hari; Helt, Gregg; Sementchenko, Victor; Piccolboni, Antonio; Bekiranov, Stefan; Bailey, Dione K; Ganesh, Madhavan; Ghosh, Srinka; Bell, Ian; Gerhard, Daniela S; Gingeras, Thomas R.

Science; 308(5725): 1149-54, 2005 May 20.

Artigo em Inglês | MEDLINE | ID: mdl-15790807

9.

Analysis of SNP content of 82 common copy-number polymorphisms from the Database of Genomic Variations.

Slater, Howard R; Bailey, Dione K; Ren, Hua; Cao, Manqiu; Bell, Katrina; Nasioulas, Steven; Henke, Robert; Choo, K H Andy; Kennedy, Giulia C.

Am J Hum Genet; 78(4): 730-1, 2006 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-16532405

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